Our Products #11810268

Oxandrolone (Anavar)

Basic Info.

Model CAS No.: 53-39-4

Customized: Customized

Puirty: >98%

Transportation: FedEx, TNT, EMS

Solubility: Soluble in Water

Successful Rate: High

Specification: BP; USP

Powder: Yes

State: Solid

Storage: Dry and Ban on Damp

Deliverytime: 3-5 Days

Shief Time: 2 Years

Form: White Crystalline Powder

safety: 100%

Transport Package: 1kg/Foilbag or According to Customer Requirements

Origin: China

Description

Anavar (Oxanabol), unlike most oral compounds is categorized as a Class I anabolic steroid, most efficiently stacked with Class II compounds such as Dianabol or Anadrol. It adds little if anything to high-dose use of Class I anabolic steroids such as or to high-dose , which is classified as having mixed activity. It can be an aid, albeit an expensive one, to moderate dose testosterone usage.

Anavar is an intriguing drug. It seems to defy the definition and limitations of oral steroids. You have read about its clean gains and relative safety. Curiously, its so safe that unlike other steroids, which were used for malnutrition and anemia, Anavar was originally prescribed mainly for burn victims. In a randomized, double-blind study, patients with 40% total body surface area burns were selected to receive standard burn care plus oxandrolone, or without oxandrolone. Oxandrolone was used to help regain weight lost after surgery, severe trauma, or chronic infections. Those treated with oxandrolone showed quickened healing, improved body composition, preserved muscle mass and reduced catabolism and consequently lessened hospital stay time.

Oxandrolone is rapidly absorbed from the gastrointestinal tract, resulting in a maximum plasma concentration between 30 and 90 minutes and a plasma half-life of about 9 hours. Oxandrolone has been given orally in the treat-ment of constitutional delayed growth and puberty in boys. Courses of treatment are short (about 3 to 4 months) because of the risk of epiphyseal closure. Oxandrolone has been prescribed to post-menopausal women in the treatment of osteoporosis. Oxandrolone is also under investigation in the treatment of Turners syndrome in girls. As oxandrolone is C17-alpha-alkylated there is the potential for liver damage.

Application

Anavar has often been called a weak steroid. Part of the reason for this is that use of a Class I steroid alone never is maximally effective. The other cause is that bodybuilders and authors in the field sometimes make unfortunate and unreasonable comparisons when judging anabolic steroids.

Oxanabol(Anavar, Oxanabol) has given optimistic consequences in taking care of anemia and hereditary angioedema. Proven studies though have given links linking expanded use of the medicine and problems of liver toxicity like to those found with additional 17-alkylated steroids. Yet in little dosages, numerous patients shown gastro-intestinal troubles such as bloating, nausea, and diarrhea. Oxanabol(Anavar, Oxanabol)`s specificity targeting the androgen receptor predestined that, unlike lot other steroids, it had not been seen to give stunted development in teens people, as well at usual measure not often observed clear masculinising reactions external of stimulating strength growth. Oxanaboldoes not aromatize at any measure, and is not without problems ingested into DHT or estrogen. As such, a typical dose of 20-30 mg offered eminent androgen levels for up to eight hours. To enlarge use, bodybuilders classical "stacked" the Oxanabol(Anavar, Oxanabol) with others such as , advance enhancing corp power increase.

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Product Name:Andarine

Andarine Alias:GTX-007;S4

Andarine CAS:401900-40-1

Andarine Molecular Formula:C19H18F3N3O6

Andarine Molecular weight:441.36

Apperance:Pale Yellow Solid

Assay:99%

Shipping Time:3-7days after payment

Delivery Methods:fedex, ems, ups, dhl, tnt ect

Andarine (GTx-007, S-4) is an investigational selective androgen receptor modulator (SARM) developed by GTX, Inc for treatment of conditions such as muscle wasting, osteoporosis and benign prostatic hypertrophy, [1] using the non-steroidal androgen antagonist bicalutamide as a lead compound.

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testosterone cypionate

testosterone cypionate quick detail::

testosterone cypionate; good quality testosterone cypionate; test cypionate;

testosterone cypionate cas no: 58-20-8

testosterone cypionate molecular formula: c27h40o3

testosterone cypionate molecular weight: 412.61

testosterone cypionate assay: 99% min

testosterone cypionate appearance: white crystalline powder

testosterone cypionate quality standard: usp32

testosterone cypionate effective dose (men): 300-2000mg+ week

testosterone cypionate packing: aluminum foil bag testosterone cypionate

testosterone cypionate min. order quantity: 10g testosterone cypionate

testosterone cypionate payment: western union ;;t/t. testosterone cypionate

testosterone cypionate shipment: ems, dhl, fedex, etc testosterone cypionate

testosterone cypionate delivery: safe & timely, around 5-7 business days door-to-door after payment

testosterone cypionate shippment policy: re-sent

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17-Methyltestosterone

Quick Detail

Product Name: 17-Methyltestosterone

Other Name: Methyltestosterone

Model NO: 58-18-4

CAS: 58-18-4

Appearance: white powder

Molecular Formula: C20H30O2

Express: EMS, DHL, FedEx, etc(Door-to-Door)

Product Description

Methyltestosterone (brand names:[1] Android, Androral, Oraviron, Testred, Virilon) is a 17-alpha-alkylated anabolic steroid used to treat men with a testosterone deficiency.[2] It bears close structural similarity to testosterone, but has a methyl group at C17 in order to increase oral bioavailability.It is used as a feed additive to produce predominately male populations of tilapia. Methyltestosterone is a 17-alpha-alkylated anabolic steroid used to treat men with a testosterone deficiency. It is also used in women to treat breast cancer, breast pain, swelling due to pregnancy, and with the addition of estrogen it can treat symptoms of menopause

A testosterone can promote male sexual organs and use for seedling stage changes. Methyl testosterone is a steroid hormone derived from androgen, present in mammals and other vertebrates. Methyl testosterone is mainly secreted in e-mail and female ovarian tests, although a small amount is also secreted by the adrenal gland, methyltestosterone is the main male sex hormone and anabolic steroids.

Methyltestosterone plays a key role in male reproductive tissue such as testicular and prostate development. In addition, methyltestosterone is essential for both health and well-being and for the prevention of osteoporosis. Methylestosterone is conserved in most vertebrates, although fish are slightly different from the so-called 11-ketone testosterone.

Mestanolone

Quick detail

Product name: Mestanolone

Model NO: 521-11-9

EINECS: 208-302-6

Molecular Formula: C20H32O2

Molecular Weight: 304.47

Melting point: 224-226C

Appearance: White or Similar crystalline powder

Mestanolone Soluble in acetone, ethanol, ethyl ether, ethyl acetate, insoluble in water

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boldenone cypionate

quick detail:

product nameboldenone cypionate

other name17beta-hydroxy-androsta-1, 4-dien-3-one cyclopentanepropionate

cas register number106505-90-2

molecular formulac26h38o3

molecular weight398.58

structureboldenone cypionate bulking cycle muscle growth steroids powder cas 106505-90-2

specification200mg/ml

appearancewhite crystalline powder

assay99%

delivery time3-7 work days

minimum order10grams

supply abilitymass in stock

payment termswestern union , , t/t , bitcoin

packingdisguised package or as required

boldenone cypionate description:

boldenone cypionate is an ester of boldenone and is recommended as an aid for the treatment of debilitated horses when an improvement in weight, hair coat or general physical condition is desired. debilitation often follows disease or may occur following overwork and overexertion.

boldenone improves the general state of debilitated horses, thus aiding in correcting weight losses and improving appetite. it is not a substitute for a well-balanced diet. optimal results can be expected only when good management and feeding practices are utilized. boldenone should be considered only as adjunctive therapy to other specific and supportive therapy for diseases, surgical cases and traumatic injuries.

boldenone 200 usp injection provides boldenone cypionate is a long acting anabolic steroid used in veterinary medicine for the treatment of horses. boldenone possess marked anabolic properties and a minimal amount of androgenic activity. boldenone has a rapid onset of action; this is advantageous and is preferred over frequent oral dosing or even repeated injections.

the esterification of the 17-beta-hydroxyl group increases the duration of the action of boldenone. boldenone esters in oil injected intramuscularly are absorbed slowly from the lipid phase, thus boldenone 200 can be administered at intervals of every 2-3 weeks.

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Stanozolol (Winstrol)

Quick Detail

Product name: Stanozolol (Winstrol)

CAS : 10418-03-8

M. F: C21H32N2O

M. W: 328.49

What is Stanozolol Winstrol and used for?

Stanozolol Winstrol is one of the most popular anabolic steroids. Stiprolol Winstrol may be administered orally or intramuscularly. Some of its therapeutic uses include treatment for aplastic anemia and hereditary angioedema. It is also indicated as adjunctive therapies for the treatment of various other medical disorders such as vascular disease and growth failure.

Like many synthetic metabolic steroids, Stanozolol Winstrol is used to treat muscle wasting disorders, burn subjects, exposure to corticosteroids and osteoporosis. It is also used to help fracture healing, even in the presence of hormonal imbalance is also successfully used for obesity treatment. Breast cancer specific forms of treatment of angioedema and even some forms of delayed growth treatment for children have been shown to be successful. Unlike many synthetic metabolic steroids in the United States, Stanozolol Winstrol has never lost FDA approval.

Application and More description for Stanozolol Winstrol

Stanozolol Winstrol Is a DHT-based anabolic steroid. Specifically, Stanozolol Winstrolis is a structural variant of DHT hormones, and two specific changes in DHT give us Stanozolol Winstrol. The first modification is the addition of the ligated pyrazole group to the 3-membered ring instead of the 3-keto group. This makes Stanozolol Winstrol a heterocyclic steroid. The second change is to add methyl. This change occurs at the 17th carbon position and Stanozolol Winstrol is placed in the 17-alpha alkylation (C17-aa) category.

The structural changes of DHT given to our Stanozolol Winstrol significantly reduced the androgen of the hormone and greatly increased its anabolic activity. Stanozolol Winstrol has an anabolic rating of 320 with an orrogen score of 20, and real-life use will match these structural ratings.

Stanozolol Winstrol has a lot of features and features that can be best viewed by looking at each person individually

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Dianabol (Metandienone)

Quick Detail

Product NameDianabol

AliasMethandrostenolone

CAS Registry Number72-63-9

Einecs No200-787-2

Molecular FormulaC20H28O2

Molecular Weight300.44

Purity>99%

GradePharmaceutical Grade

AppearanceWhite Powder

Melting Point164.5-165.5C

Specific Rotation+9.3.0

Loss On Drying0.21%

Residue on ignition0.05%

Residual Solvents210ppm

Heavy Metals

Drostanolone Propionate (Masteron)

Product name: Drostanolone propionate

Alias: Masteron

CAS No: 521-12-0

Einecs No: 208-303-1

MF: C23H36O3

MW: 360.53

Appearance: white crystalloid powder and yellow liquid

Usage: As a therapeutic agent, Masteron enjoyed two decades of success in combating advanced inoperable breast cancer in postmenopausal women. It would also become a popular cutting steroid among bodybuilders, which is where Masteron is currently most commonly found.

Masteron description

Originally Dromostanolone (abbreviated to Drostanolone) known by trade name Masteron is an injectable oil-based anabolic steroid, derived from Dihydrotestosterone (DHT). It is a member of the DHT-derived family of anabolic steroids. Other known DHT-derivatives include: Winstrol, Anadrol, Anavar, Primobolan, and a few more. Drostanolone (Masteron) is considered a moderate strength anabolic steroid with anabolic rating: 62 - 130 and low androgenic strenght: 25 - 40.

There are two different variants of Masteron

Drostanolone Propionate

Drostanolone Enanthate

All anabolic steroid analogues and derivatives are derivates of the three natural anabolic steroids found in the human body:

Testosterone

Dihydrotestosterone

Nandrolone

Drostanolone is injected into the body as an ester (bonded to either Propionate or Enanthate). Enzymes cleave off the ester from the Masteron molecule - which takes varying amount of time depending on which ester was used. This process causes the gradual release rate and extended half-life of the steroid. Drostanolone Propionate has a half-life of 2.5 days, while Drostanolone Enanthate has a half-life of 10 days.

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Chemical Name :(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-cyanophenoxy)-2-hydroxy-2-methylpropanamide

Common Name MK-2866 (GTx-024) / Ostarine / Enobosarm

CAS 1202044-20-9

CAS:841205-47-8

MF C19H14F3N3O3

MW 389.3279696

Product Categories Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Hormone Drugs;SARMs(Selective androgen receptor modulator)

Appearance : Almost white or white powder

Purity 99.59%

Usage Nonsteroidal selective androgen receptor modulator (SARM) used in the treatment of osteoporosis and muscle wasting in animal models.

A potential compound for the treatment of hypoactive sexual desire disorder.

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Anabolic Steroid Sarms Raw Powder , MK 677 Ibutamoren Nutrobal Bodybuilding CAS 159752-10-0

MK-677 Alias:Ibutamoren

MK-677 CAS:159752-10-0/159634-47-6

MK-677 Molecular Formula:C27H36N4O5S.CH4O3S

MK-677 Molecular weight:624.776

Apperance:White Fine Powder

Assay:99%

MK-677 quality: 624.22900 PSA: 196.66000 LogP: 4.97440

MK-677 boiling point: 868.9C at 760 mmHg

MK-677 flash point: 479.3C

MK-677 vapor pressure: 3.05E-32mmHg at 25C

MK677 color: off-white powder or light yellow powder

Here are the anecdotal MK 677 dosage guidelines:

Beginner: 10 mg per day

Intermediate: 25 mg per day

Advanced: 50 mg per day

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Methoxydienone

Synonyms: 13-beta-ethyl-3-methoxygona-2, 5(10)-dien-17-one

CAS: 2322-77-2

EINECS: 219-034-4

MF: C20H28O2

MW: 300.44

Methoxydienone Steroid Intermediate Most Powerful Prohormones For Mass CAS 2322-77-2

Assay: 90% min.

Packing: 1kg net/foil bag or 10kg net/tin.

State:Solid

Shipping Method:EMS, FedEx.TNT, DHL and So on

Express Courier:Hkems, DHL, FedEx, UPS, TNT

Certificate:ISO9001, Kosher, Reach

Character: White crystalline powder. Melting point 150-160

Usage: 18-levonorgestrel, Gestrinone intermediates.

Description

Methoxydienone particular to a process of synthesis of levonorgestrel, Levonorgestrel is a quick, short-term oral contraceptives, contraceptive mechanism is significantly inhibit ovulation and prevent embryo implantation, and to increase the consistency of the cervical mucus, sperm penetration resistance increases, and thus play a fast-acting contraception.

Methoxydienone is a progestin derived steroid and not a 17-alpha alkylated steroid. Methoxydienone is structurally related to RU-486 and acts as an antiprogesterone, decreasing estrogen-like effects. Great for those needing fast weight gain and unconcerned about looking smooth or fat.

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CAS No.: 315-37-7

M.F.: C26H40O3

M.W.: 400.59

Reference Standard: EP5

Appearance: White to yellowish-white crystalline powder

Dosage:Average Dose: Men 250-1000 mg/week

Half life: 15-16 days

Usage: Testosterone Enanthate is a slow acting release form of the testosterone hormone, and is one of the most commonly used testosterones to treat the people lacking of testosterone .The side effect of using testosterone enanthate we are easy to control . Everyone like it because it was necessary .

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Oxymetholone (Anadrol)

CAS:434-07-1

MF:C21H32O3

MW:332.48

EINECS:207-098-6

Melting point:172-180C

alpha 34

Boiling point:409.59C (rough estimate)

Density 1.0834 (rough estimate)

refractive index 38 (C=1, CHCl3)

storage temp. 2-8C

solubility H2O: 0.5 mg/mL

form solid

color white to light yellow

The Benefits of Anadrol:

As a steroid designed to treat weight deficiency and muscle wasting disease this is one of the more prominent bulking steroids we can use for a bulking purpose. While many anabolic steroids can serve both bulking and cutting purposes most have a primary role and Anadrol makes no exception. There is one purpose for Anadrol while on a cutting cycle and we will touch on it as we go but for the majority of steroid users bulking and only bulking will be the only time they use this steroid.

With its immense power, Anadrol is one of the most powerful oral steroids ever made, individuals can see their weight increase by as much as 20-30lbs in a mere few weeks of use as well as see their strength shoot through the roof. Further, as this steroid is almost always used as part of a stack and not alone, due to its low androgen binding characteristics it will allow other steroids you are taking to more aptly fill this role and more or less create a higher level of synergy between the various anabolic androgenic steroids you are taking.

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Fluoxymesterone (Halotestin)

Quick details

Product Name: Fluoxymesterone

Alias: Halotestin, Halotestin

CAS No: 76-43-7

Einecs No: 200-961-8

MF: C20H29FO3

MW: 336.44

Purity: 99%

Appearance: white powder.

Use: Fluoxymesteron Powder For Cutting Cycles Halotestin Steroids

Grade: Pharmaceutical grade

Package: Disguised package ; Foil bag

Certificate: ISO 9001, USP, GMP

Product description

Fluoxymesteron is an extremely powerful synthetic metabolic androgen steroid, released by Upjohn for the first time by trade name Halotestin in the late 1950s. Soon after, Ciba Pharmaceuticals will release hormones under the Ultandren name, but Halotestin is still the most well-known brand. Pharmacia, formerly known as Upjohn, now manufactures Halotestin brand names.

Halotestin is one of the most powerful synthetic metabolites present. Despite its strength, it only has some favorable features for most individuals, making it a poor choice for most athletes to improve performance. The average gym mouse does not find this is a steroid he wants to include in his cycle. There is no strategic advantage, the risk is far more than the reward. The average athlete's rat can easily reach his target with the use of other compounds. Of course, some gymnasium rats try to try it, the strength of the rapid and dramatic increase sounds attractive, but it is important to remember the harsh nature of this steroid.

Fluoxy is a synthetic androgen steroid hormone that can be obtained by formulation. It can be given to men who have the medical condition of women who reduce or inhibit the production of testosterone naturally or have certain forms of breast cancer. Health care providers often warn that the drug may cause various possible side effects and may not be recommended for use in certain patients, due to potentially serious side effects.

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product name: lidocaine hcl

other name: lidocaine hydrochloride

cas: 73-78-9

appearance: white crystals powder

purity: 99%

trademark: pharmlab

original: china

grade: pharmaceutical grade

package: disguised package ; foil bag

delivery date: 3-5 work days

certificate: iso 9001, usp, gmp

payment: western union, , t/t, bitcoin

shipping: ems, hkems, eub, etk, fedex, dhl, ups, aramex, etc

policy: re-shipping policy

mf: c14h23cln2o

mw: 270.7982

melting point: 350.8 c at 760 mmhg

usage: local anesthetics, antiarrhythmic drugs, used for a variety of anesthesia and rapid ventricular arrhythmia

product description

lidocaine hydrochloride is a local anesthetic is characterized by rapid onset and mid-term efficacy. thus, lidocaine is suitable for osmotic, obstructive and topical anesthesia. long-acting substances such as bupivacaine are sometimes given priority to subdural and epidural anesthesia. on the other hand, lidocaine has the advantage of rapid onset. it can prevent adrenaline vasoconstriction formation bleeding, may also delay the absorption of lidocaine, anesthesia duration almost doubled. for surface anesthesia, several formulations that can be used can be used. g. for endoscopy, before intubation. the ph of the buffered lidocaine makes the local freezing less painful. lidocaine eye drops can be used for eye short ophthalmic surgery.

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Product Name:Yohimbine Hydrochloride

Synonyms:Corynine hydrochloride;Aphrodine hydrochloride;Aphrosol hydrochloride;

17-hydroxyyohimban-16-carboxylic acid methyl ester hydrochloride;

17a-hydroxyyohimban-16a-carboxylic acid methyl ester hydrochloride;

Yohimbe hcl;Yohimbine hcl

CAS:65-19-0

EINECS:200-600-4

MF:C21H27ClN2O3

MW:390.9

Molecular Structure:98% Purity Natural Plant Extract Yohimbine Hydrochloride for Neurological Disorders

Grade:Pharmaceutical grade

Standard:Enterprise Standard

Assay:98%

Appearance:White to slightly yellow powder

Solubility:H2O: 10 mg/mL

Usage:Indole alkaloid with 2-adrenergic blocking activity. Mydriatic. Used in the treatment of neurological disorders.

Packing:1kg/Foil bag

First, Yohimbine HCl must NOT be taken with food or vitamin supplements of any kind. It must be taken by itself on an empty stomach in between meals or in a fasted state when you first wake up in the morning. It also is best to spread dosing throughout the day as this also helps with its appetite suppressing effects which will help maximize your weight loss when taking it.

The minimum dosing is set at 5 mg per day, with 2.5 mg taken 2 times per day on an empty stomach in between meals as described above. Wait at least 20-30 minutes until you eat after administration.

Maximum Results: In order to achieve the maximum effects when taking this supplement, the following dosing guidelines should be met.

Dosages of 0.2mg/kg bodyweight have been successfully used to increase fat burning without significant implications on cardiovascular parameters like heart rate and blood pressure. This results in a dosage of: 14 mg for a 150lb person, 18 mg for a 200lb person, and 22 mg for a 250lb person.

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Product Name: Tween 80

Synonyms: armotanpmo-20;atlox1087;atlox8916tf;atolox8916tf;capmulpoe-o;crill10;crill11;crillet4

CAS: 9005-65-6

MF: C24H44O6

MW: 428.600006103516

EINECS: 500-019-9

Product Categories: Ester Ether Type (Surfactants);Functional Materials;Nonionic Surfactants;Surfactants;Biochemistry;Nonionic Surfactants (for Biochemistry);Surfactants (for Biochemistry);Cosmetic Ingredients & Chemicals;detergent;emulsifier

bp >100C

density 1.08 g/mL at 20 C

vapor pressure 230 F

storage temp. Store at RT.

form viscous liquid

Water Solubility 5-10 g/100 mL at 23 oC

Merck 14, 7582

Chemical Properties Yellow to amber liquid

Product Categories: Ester Ether Type (Surfactants);Functional Materials;Nonionic Surfactants;Surfactants;Biochemistry;Nonionic Surfactants (for Biochemistry);Surfactants (for Biochemistry);Cosmetic Ingredients & Chemicals;detergent;emulsifier

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Name: SR9009

Synonyms: Stenabolic

CAS No.: 1379686-30-2

Molecular formular: C20H24ClN3O4S

Molecular Weight: 437.94

Appearance: White powder

Purity: 99%

Application: SR9009 increase exercise endurance and loss weight.

Dosages of 20-100mg a day have been reported by users without any negative side effects. From the information we have received, results from SR9009 treatment appear to be dose dependent up to a maximum dosage of 100mg per day. After this dosage, results tend to taper off.

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Quick Detail

Product Name: L-Carnitine

CAS:541-15-1

Assay: 99%

MF: C7H15NO3

MW: 161.2

EINECS: 208-768-0

Chemical Properties: White crystalline

Sample: Available

Storage: Cool and Dry Place

Trademark: Pharmlab

HS Code: 2923900090

Suitable for: Elderly, Adult

Usage: Body Slimming, Weight Loss, pharmaceutical raw materials, the hormone

OEM Service: Available

Shelf Life: 36 Months

Overview

1. Carnitine is a kind of B-class vitamin. Owing to its similar structure as amino acids, some people therefore also classify it as an amino acid. Its main function is to supply energy through facilitating the transport of long chain fatty acids. This prevents the fat accumulation in the heart, liver and skeletal muscle. It can control diabetes, fatty liver, and the fat metabolism disorder in heart disease. Taking carnitine can reduce damage to the heart. It can lower the level of blood triglyceride and also have certain role in boosting weight loss. Carnitine can further enhance the antioxidant effect of vitamin E and vitamin C.

2. Carnitine deficiency is sometimes congenital such as genetically deficiency of carnitine synthesis with symptoms including heartburn, muscle atrophy and obesity. Men need more carnitine than women. Vegetarian are more prone to get carnitine deficiency.

3. If the body has sufficient iron, thiamin, vitamin B6, lysine, methionine and vitamin C, carnitine would not be lacking. Carnitine-rich foods contain meat and offal.

4. Synthetic carnitine is divided into three forms including L-body, dextral and racemic with L-carnitine having the best efficacy.

5. L-carnitine is a kind of compound with various kinds of physiological activities. Its major function is to promote the beta-oxidation of fatty acid as well as regulate the acyl ratio inside mitochondrial to affect the energy metabolism. L-carnitine can participate in the transport of branched chain amino acid metabolites, and thus promoting the normal metabolism of branched chain amino acids. In addition, L-carnitine can take effect in the elimination and utilization of ketone bodies and play a role of biological antioxidants for scavenging free radicals, maintain the stability of the membrane, improve animal's immunity and the ability of anti-stress and disease resistance.

6. L-carnitine is not a weight loss drug. Its main role is to burn fat which is not the same thing as losing weight. To use L-carnitine for losing weight, in addition to burning fat with its help, a lot of movement is still the key for weight loss; instead carnitine only play a supporting role. If exercise is

product name: theobromine

other name: 3, 7-dimethylxanthine, 3, 7-dihydro-3, 7-dimethyl-1h-purine-2, 6-dione

cas: 83-67-0

appearance: white crystals powder

purity: 99%

trademark: pharmlab

original: china

grade: pharmaceutical grade

package: disguised package ; foil bag

delivery date: 3-5 work days

certificate: iso 9001, usp, gmp

payment: western union, , t/t, bitcoin

shipping: ems, hkems, eub, etk, fedex, dhl, ups, aramex, etc

policy: re-shipping policy

mf: c33h57n11o9

mw: 751.9

product description

theobromine, formerly known as xanthate, is a bitter alkaloid of a cocoa plant with a chemical formula of c7h8n4o2. it is classified as a xanthine alkaloid, which also includes similar theophylline compounds. the degree of methylation of the compounds is different.

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Product Name:Paracetamol

CAS:103-90-2

MF:C8H9NO2

MW:151.16

EINECS:203-157-5

Appearance:White powder

package:25kg/bag

Grade:Pharmaceutical grade

Usage:AcetanilidesAnalgesicsAntipyretics

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Ropivacaine hydrochloride

Synonyms: S-ROPIVACAINE HCL;

CAS: 132112-35-7

MF: C17H26N2O.ClH.H2O

MW: 328.88

Product Categories: Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals

Mol File: 132112-35-7.mol

use:anesthetic (local), Pharmaceutical raw materials

Packing:Foil bag or as requirments

Ropivacaine hydrochloride-------Clinical Use:

1. Ropivacaine is indicated for local anaesthesia including infiltration, nerve block, epidural and intrathecalanaesthesia in adults and children over 12 years. It is also indicated for peripheral nerve block and caudalepidural in children 1-12 years for surgical pain.

2. It is also sometimes used for infiltration anaesthesia for surgical pain in children.Ropivacaine is often coadministered with fentanyl for epidural analgesia, for example in pregnant women during labour.

chloroprocaine hydrochloride / chloroprocaine hcl

cas no.: 3858-89-7

m.f: c13h20cl2n2o2

m.w: 307.21600

pure content: 99%

appearance: white crystalline powder

minimun order quantity: 100 gram

certification: iso 9001, iso 14001, gmp

usage: muscling

qulification: usp

delivery method: hkems, dhl, tnt, ups, fedex, ems etc. by air or by sea.

delivery time: 5-14 working days, tracking number available

payment terms: t/t, , western union and bitcoin

origin: hubei province, china

brand name: pharmlab

production capacity: chloroprocaine hcl 500kg/month

what is chloroprocaine hydrochloride?

chloroprocaine hydrochloride is a short-acting spinal anesthesia performed under the waist. anesthesia of spinal nerves using spinal anesthesia, so that patients remain sober, but in the course of surgery will not be pain.

application

chloroprocaine (trade name nesacaine, nesacaine-mpf) (usually in the form of hydrochloride in the above-mentioned trade name) is a local anesthetic administered by injection during surgery and during childbirth.

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product name: creatine monohydrate

other name: n- methyl guanidine acetic acid, creatine, creatine, sarcosine methyl guanidine acetic acid

cas: 6020-87-7

appearance: white crystals powder

purity: 99%

trademark: pharmlab

original: china

grade: pharmaceutical grade

package: disguised package ; foil bag

delivery date: 3-5 work days

certificate: iso 9001, usp, gmp

payment: western union, , t/t, bitcoin

shipping: ems, hkems, eub, etk, fedex, dhl, ups, aramex, etc

policy: re-shipping policy

molecular formula: h2o - c4h9n3o2

molecular weight: 149.15

uses: 1 food additives, cosmetic surfactants, feed additives, beverage additives, pharmaceutical raw materials and additives, can also be directly made capsules, tablets, oral.

creatine monohydrate ------------introduction

water creatine is a medicinal raw material and health care additive. can inhibit the production of muscle fatigue factors, relieve fatigue and tension, restore the body, can speed up the body protein synthesis, make muscle stronger, enhance muscle elasticity, lower cholesterol, lower blood lipids, lower blood sugar levels, improve the elderly blood sugar muscle nutrition bad, anti-aging.

creatine monohydrate is a dietary supplement for athletes and many bodybuilders used to increase high-intensity exercise performance, increase strength, have more muscle, increase body mass and faster muscle recovery after exercise.

creatine monohydrate----------- nutrition supplements

creatine is creatively known as the most popular and effective nutritional supplements. highly enough to keep up with the status of protein products, ranking "best-selling supplements" list. was rated as "must use" the body, there are other items of athletes, such as football, basketball players, etc., want to improve their energy level, the power of people widely used.

the chemical name of creatine is methyl guanidine-acetic acid. creatine is a natural substance found in our muscle cells, especially around skeletal muscle (about 95% of the body's creatine supply) and the remaining 5% in other parts of the body. creatine is a metabolite produced by the body, consisting essentially of three amino acids - methionine, arginine and glycine.

our liver has the ability to combine these three amino acids and creatine. the pancreas and kidneys also synthesize a small amount of creatine when necessary. another source of creatine is our diet. we can also obtain creatine by using it as a dietary supplement. although it has many different forms, the most commonly used formula for sports purposes is creatine monohydrate.

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Product Name:Casein Protein

Synonyms:Caseins;CASEIN;CASEIN 2;CASEIN 1;CASEIN-AGAROSE;CASEIN, VITAMIN FREE;CASEIN, NEW ZEALAND;CASEIN(MILK)

CAS:9000-71-9

MF:C47H48N3NaO7S2

MW:0

EINECS:232-555-1

Purity:98%

Appearance:White powder

Grade:Food Grade

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Product Name: Vitamin B12

Synonyms: Cyanocobalamin

CAS: 68-19-9

MF: C63H88CoN14O14P

MW: 1355.37

EINECS: 200-680-0

mp: >300C

storage temp: 2-8C

solubility: Soluble

Water Solubility: Soluble

Appearance: Dark Red Powder

Trademark: Pharmlab

Origin: China

Description

Vitamin B12 is a cyanide ion substituted cobalamin derivative (cyanocobalamin) with the presence of cobalt mineral at 6 position. Vitamin B12 is the only vitamin which contains metal ion (trivalent cobalt). Cobalamin is sometimes defined as the synonym of Vitamin B12, although they are not same compound but closely related compounds to fulfill folic acid role. Vitamin B12 is typically any substituted cobalamin derivative having similar biological activity. Hydroxocobalamin (abbreviated OHCbl), a cobalamin derivative in which the substituent is a hydroxyl group, is called vitamin B12b.

Vitamin B12 is a water soluble with a key role in the normal functioning of the and , and for the formation of . It is one of the eight . It is normally involved in the of every of the body, especially affecting synthesis and regulation, but also synthesis and energy production.

Vitamin B12 is the name for a class of chemically-related compounds, all of which have vitamin activity. It is structurally the most complicated vitamin. of the basic structure of the vitamin can only be accomplished by , but conversion between different forms of the vitamin can be accomplished in the human body. A common synthetic form of the vitamin, , does not occur in nature, but is used in many pharmaceuticals, supplements and as food additive, due to its stability and lower cost. In the body it is converted to the physiological forms, and leaving behind the albeit in minimal concentration. More recently, methylcobalamin and, adenosylcobalamin can also be found in more expensive pharmacological products and food supplements. The utility of these is presently debated.

Historically, vitamin B12 was discovered from its relationship to the disease , which is an autoimmune disease that destroys parietal cells in the stomach that secrete intrinsic factor. Intrinsic factor is crucial for the normal absorption of B12, therefore, a lack of intrinsic factor, as seen in pernicious anemia, causes a vitamin B12 deficiency. Many other subtler kinds of , and their biochemical effects, have since been elucidated.

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CAS No.53-41-8

SynonymsU 6036;U 60366;Androtin;NSC 9898;Androtine;Androkinin;Androkinine;Androtin-d5;Androstrone;Atromide ICI

CBNumber:CB9853748

Molecular Formula:C19H30O2

Formula Weight:290.44

MOL File:53-41-8.mol

Melting point:181-184 C(lit.)

alpha 96 (c=1, C2H5OH)

Boiling point:372.52C (rough estimate)

Density 1.0320 (rough estimate)

refractive index 1.4709 (estimate)

storage temp. 20C

form neat

Merck 13, 645

BRN 2217626

CAS DataBase Reference53-41-8(CAS DataBase Reference)

Chemical Properties

white to light beige crystalline powder

Uses

It was isolated from male urine after removed of the phenolic estrogen fraction.

Uses

Antihypertensor

Definition

ChEBI: An androstanoid that is 5alpha-androstane having a hydroxy substituent at the 3alpha-position and an oxo group at the 17-position. It is a metabolite of dehydroepiandrosterone .

Purification Methods

Crystallise androsterone from Me2CO/Et2O or Me2CO and sublime it in high vacuum. The acetate [1164-95-0] crystallises from Et2O, Me2CO/Et2O or aqueous EtOH and sublimes in high vacuum with m 165-166o, [] D 25 +87o (c 2, EtOH). [Ruzicka Helv Chim Acta 17 1389 1934, Marker J Am Chem Soc 57 1755 1935, Gnds & Orr J Chem Soc Chem Commun 1239 1982, Beilstein 8 IV 462.]

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Letrazole (Femara)

Quick detail

Prodcut name: Letrazole

Other name: Femara

CAS: 12809-51-5

Appearance: White powder

Grade: Pharmaceutical grade

Package: Disguised package ; Foil bag

Delivery date: 3-5 work days

Purity: >99%

MF: 306.44

MW: 285.30274

Prodcut description

Letrazole Is a powerful aromatase inhibitor that has been developed for the fight against breast cancer. For athletes and bodybuilders, it is a medicament for estrogen side effects against synthetic metabolic steroids, acne and celiac disease. Due to decreased estrogen in the body, can also cause elevated testosterone levels. Side effects include reduced sexual behavior and continuous use can lead to reduced lipid function and impaired immune system.

Femara is only used for women without childbearing age. Possible candidates must no longer have menstruation. Often used in patients who have received other cancer treatments, such as radiotherapy, chemotherapy, and other cancer drugs such as tamoxifen. This non-steroidal aromatase inhibitor can help prevent any remaining cancer cells from spreading.

Femara is used to treat postmenopausal breast cancer.

Product application

Letrazole Is a type II (nonsteroidal) third generation aromatase inhibitor. Clinically used for the treatment of estrogen receptor-positive or estrogen receptor unknown breast cancer in postmenopausal women.

In women with breast cancer, estrogen levels have been reduced by more than 98%.

However, its use is not limited to the elimination of estrogen in women.

For the bodybuilder before the game, Femara is almost necessary to eliminate water retention conditions, and to achieve in today's fitness world in the necessary torn appearance of competition. However, according to my experience, only need to use in the past 4-6 weeks to eliminate excessive estrogen and water retention. After using Femara, I recommend not to suppress any estrogen for at least a month in an attempt to normalize the body.

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hydrochloride

English Synonyms: DAPOXETIN;;(S-(+)-N, N-Dimethyl-a-[2-(naphthalenyloxy)ethyl]benzenemethanamine hydrochloride; hydrochloride

CAS NO.: 119356-77-3

Assay: 99%

Molecular Formula: C21H23NO HCL

Molecular Weight: 341.88

Packing: 1kg/ Foil Bag

Appearance: This product is light yellow powder, odorless, sweet, soluble in water, alcohol. Can be made into tablets, beverages, wine, capsules and other dosage forms

Usage: () as a new fast SSRI, a short half life, a selective 5 - HT reuptake inhibitor (SSRI), for the treatment of premature ejaculation and erectile dysfunction. is a selective 5 - HT reuptake inhibitor (SSRI), such drugs widely used to treat depression and related affective disorders

hydrochloride is a drug that is used to treat premature ejaculation in men. It is available by prescription and is taken orally, prior to sexual intercourse. The drug belongs to the class called serotonin reuptake inhibitors (SSRIs), which have mainly been used to treat depression.

Sexual dysfunction, including premature ejaculation, is an extremely common condition worldwide. The cause of premature ejaculation has not been fully elucidated, but may include both psychological and physiological factors. Premature ejaculation refers to a short ejaculation time, which can affect the satisfaction of both partners during sexual intercourse.

How to use :

The best time to consume is to take the drug 60 to 120 minutes before the planned sex. is capable to delay the ejaculate after penetration hence providing more time to the couple to enjoy and have fun. However, in most men the effect loses after 3 to 5 hours however some have claimed to retain the effect for as long as 8 hours. Research has revealed that , in its oral form has found to give better result in more than 75% of men. However, it may react in different person with different intensity, but has found to provide satisfactory results in most of the cases.

Dutasteride (Avodart)

English Synonyms: (5alpha, 17beta)-n-2, 5-bis(trifluoromethyl)phenyl-3-oxo-4-azaandrost-l-ene-17-carboxamide;DUTASTERIDE;GG-745, GI-198745, ;5, 17)-N-[2, 5-Bis(trifluoromethyl)phenyl]-3-oxo-4- Aza -androst-1-ene-17-carboxamide;Duagen;(5a, 17)-N-[2, 5-Bis(trifluoromethyl)phenyl]-3-oxo-4-azaandrost-1-ene-17-carboxamide;Avodart;GI 198745

CAS NO.: 164656-23-9

Assay: 99%

Molecular Formula:C27H30F6N2O2

Molecular Weight:528.53

Packing:1kg/tin/foil bag

Standard: Enterprise/USP

Appearance: White or almost white crystalline powder

Usage: Prostate enlargement, male pattern hair loss, seborrheic alopecia, hereditary hair loss

1. Prostate enlargement

Dutasteride is useful for treating benign prostatic hyperplasia (BPH); colloquially known as an "enlarged prostate".

2. Prostate cancer

In those who are being regularly screened, 5-reductase inhibitors such as finasteride and dutasteride reduce the overall risk of being diagnosed with prostate cancer; however, there is insufficient data to determine if they have an effect on the risk of death and may increase the chance of more serious cases.

3. Pattern hair loss

Dutasteride is approved for the treatment of male androgenetic alopecia in South Korea at a dosage of 0.5 mg per day. It has been found in several studies to improve hair growth in men more rapidly and to a greater extent than 2.5 mg/day finasteride.Dutasteride has also been used off-label in the treatment of female pattern hair loss.

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Name:Finasteride

Alias:Finasteride

CAS:98319-26-7

Assay:>99%

Appearance:White crystalline powder

Molecular Formula:C23H36N2O2

Standard:SGS, GMP, ISO9001

Origin:China

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Benzyl Benzoate

CAS No.:120-51-4

EC No.: 204-402-9

Molecular formula: C14H12O2

Molecular weight: 212

Properties: In standard conditions, benzyl benzoate is a colorless or pale yellow viscous transparent liquid. In temperature conditions of 17 degrees centigrade or lower, it will be solidified into white solid. Benzyl benzoate of high-purity would send out slight fragrance.

Freezing point: 17C

Boiling point: 323C

Solubility: Benzyl benzoate is insoluble in water but soluble in organic solvents. Benzyl benzoate itself, a high-temperature solvent, is the only solvent of Musk. Benzyl benzoate has applications to pharmacy and perfume industry just because of its characters of low volatilization and relative stability.

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Product name: Grape seed oil

Alias: Vitis vinifera

CAS: 85594-37-2

Einecs: 287-896-9

MW: 428.65

Purity: 99%

Appearance: Pale Yellow Liquid

Refractive Power: 1.470-1.475

Relative Density (20 ) 0.915 0.925

Refractive index (20 ) 1.4700 1.4750

Linoleic acid (%) 70 76

Grade: Natural Plant Extract; Flavors & Fragrances

Storage: The oil should be stored at a cool and dry place, protected from light.

Shelf life: The shelf life of the oil is two years if unopened in the original package. Once opened the oil should be Blanketed under nitrogen and used within six months.

1. Grape seed through the most advanced cold pressing method and refined, is one of the very popular in the base oil and the effect is outstanding varieties. Grape seed oil is a natural non-toxic properties, children, pregnant women, the elderly and athletes are applicable.

2. Atioxidant, dilute the stain.

3. Endocrine disorders caused by dry skin, reduce melanin, whitening skin, removing chloasma.

4. To stimulate cell division and tissue regeneration, activation of the surface cells, reduce wrinkles, delay aging.

5. Inhibit and remove the body of free radicals, anti-cancer anti allergic effect.

6. Anti prostate cancer, the role of anti liver tumor, but also against damage to the nervous system.

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Ethyl Oleate

Alias: (Z)-9-Octadecenoic acid ethyl ester Ethyl, 9-octadeceneoate

Purity : 98.0%

CAS Registry Number: 111-62-6

MF: C20H38O2

MW: 310.51

Grade : Pharmaceutical Grade

Storage: Shading, confined preservation

Lead time :within 24 hours upon receipt of payment

Appearance: clear pale yellow oily liquid

Usage: It was obtained by the hydrolysis of various animal and vegetable fats and oils.

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product name: guaiacol

purity: 99%

cas: 90-05-1

appearance: white or light yellow crystalline or colorless to pale yellow transparent oily liquid

trademark: pharmlab

original: china

grade: pharmaceutical grade

package: disguised package ; foil bag

delivery date: 3-5 work days

certificate: iso 9001, usp, gmp

payment: western union, , t/t, bitcoin

shipping: ems, hkems, eub, etk, fedex, dhl, ups, aramex, etc

guaiacol mf: c7h8o2

guaiacol mw: 124.14

guaiacol einecs: 201-964-7

product categories: pharmaceutical intermediates;aromatic ethers;aromatics

compounds;antioxidant;biochemistry;aromatics

mp: 26-29 c(lit.)

bp: 205 c(lit.)

density 1.129 g/ml at 25 c(lit.)

storage temp. refrigerator

chemical properties light yellow oil

usage: gb 96 - 2760 for the temporary use of edible spices. mainly used in the preparation of coffee, vanilla, smoked tobacco and tobacco and other flavor. can also be used in medicine, dyes and spices intermediates .

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Product name:Polyethylene glycol

Other name:Alcox E 30; alcoxe30; alkapolpeg-200;

CAS register number:25322-68-3

EINECS:200-849-9

Molecular formula:HO(CH2CH2O)nH

Molecular weight:380-420

Melting point:typically near 8C

Reacted with fatty acid to make different performance surfactant, PEG can be used as a pharmaceutical binder, cream and shampoo base material. Used as lubricants, binders and plasticizers, wetting agents for fiber processing, pottery, metal processing, rubber molding, and also it can be used in water soluble paints and printing inks. Used as a wetting agent in the electroplating industry.

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DMAA (1, 3-dimethylamylamine) is an amphetamine derivative that has been widely used in sports supplements sold in the United States. Also known as methylhexanamine or geranium extract, DMAA is often touted as a natural stimulant, with many claimed functional uses including a body-building aid, an athletic performance enhancer, and a weight-loss aid. Although DMAA at one time was approved as a drug for nasal decongestion, no medical use of DMAA is recognized today. FDA is not aware of any reliable science indicating that DMAA exists naturally in plants.

Using and Dosage

A typical starting dose of 1, 3-DMAA is in the 10-20mg range and eventually reaching up to 40-60mg a day, there is no actual evidence to support this dosage range but it seems to be the standard dosages range for supplemental 1, 3-DMAA on the market.

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Rimonabant (Acomplia) Details:

Product Name:Rimonabant

CAS:168273-06-1

Purity:99.43%

MF:C22H21Cl3N4O

MW:463.79

Appearance:White to off white powder

Melting point:272.25C

Usage:Fat burn

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product name: cla

other name: conjugated linoleic acid

cas: 2420-56-6

mf:c18h32o2

mw:280.45

einecs:607-342-5

flash point:14

storage temp. 20c

appearance: pale yellow liquid

purity: 99%

trademark: pharmlab

original: china

grade: pharmaceutical grade

package: disguised package ; foil bag

delivery date: 3-5 work days

certificate: iso 9001, usp, gmp

payment: western union, , t/t, bitcoin

shipping: ems, hkems, eub, etk, fedex, dhl, ups, aramex, etc

policy: re-shipping policy

product description

cla is a fatty acid found in beef and milk fat. in 1988, when the university of wisconsin researchers in the fried burgers in the rat study found its antioxidant properties, the cla's scientific interest to be stimulated. cla can not be produced by the human body, but can be through whole milk, butter, beef and lamb and other food to get. cla may be one of the most effective antioxidants in our diet.

in the preliminary study, cla has also been shown to reduce the body fat of overweight people. cla may be beneficial in other areas, including prevention of breast and colon cancer. other potential benefits include reduced food-induced allergic reactions, and overall enhancement of the immune system.

product stocking

conjugated linoleic acid (cla) is a family of at least 28 linoleic acid isomers, found primarily in ruminants of meat and dairy products. cla can be cis or trans fats, and the double bonds of cla are conjugated and separated by their single bonds.

the product should be stored in a gas-tight barrel under nitrogen to reduce oxidation. the product should not be stored in uncoated drums.

cla is sold as a dietary supplement based on its assumed health benefit. however, there is no convincing evidence that taking cla supplements is good for human health.

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product name: orlistat

cas: 96829-58-2

mf: c29h53no5

mw: 495.73

einecs:639-755-1

purity: 99%

appearance: white crystals powder

grade: pharmaceutical grade

certificate: iso 9001, usp, gmp

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orlistat introduciton

orlistat blocks some of the fat which you eat, keeping it from being absorbed because of your body. orlistat is used to aid in weight reduction, or to lessen the risk of regaining weight lost.

this medicine is employed together with a reduced-calorie diet. orlistat is good for use only in grown-ups. orlistat (prescription and nonprescription) is utilized with an individualized low-calorie, low-fat eating and working out program to help lose weight. prescription orlistat is used in overweight people who can also have high blood pressure, diabetes, high-cholesterol, or coronary disease.

orlistat is also used after weight-loss to help keep from gaining back that weight. orlistat is within a class of medications called lipase inhibitors. it functions by preventing a number of the fat in foods eaten from being absorbed from the intestines. this unabsorbed fat will be removed from our bodies in the stool.

orlistat is currently internationally recognized as a new type of weight loss lipid-lowering drugs with the marketed product being under the name of xenical. it was first listed in new zealand in 1998 with annual sale of $ 146 million at that time. in 2007, the sale reaches $ 538 million, orlistat occupy 80% of the market share of the global weight-loss market with the annual sale of only china hong kong year reaching 80 million us dollars.

orlistat is a long-acting and potent specific inhibitor of gastrointestinal tract lipase, appearing as white or white-like powder at room temperature and being insoluble in water, soluble in chloroform and easily soluble in ethanol. it can form covalent bonds with the active serine sites of the gastric lipase and the pancreatic lipase in the stomach and small intestine cavity, resulting in inactivation of the enzymes. fat in food cant be broken down into free fatty acids and monoacylglycerols so that the fat cant be absorbed and utilized, thereby having reduced the body's calorie intake to control the body weight.

the drug does not need to be absorbed through the body. at normal doses, the absorption of fat can be inhibited by 30%. there is little absorption after oral administration. it can be subject to metabolic inactivation in the intestine with the metabolic sites located in the gastrointestinal wall. the elimination half-life is about 14 to 19 hours. about 97% of the goods are excreted with the feces, of which 83% are in the prototype.

clinically orlistat can be applied to the treatment of obesity and hyperlipidemia. under normal circumstances, it can be subject to oral administration at a dose of 120 mg for three times per day. take it during the meal or 1 hour after a meal. after 2 weeks of administration, the body weight can begin to decline. it can be taken continuously for 6 to 12 months. if the dose is increased to above 400 mg daily, the effect will no longer be further enhanced.

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cas:94-09-7

mf:c9h11no2

mw:165.19

einecs:202-303-5

melting point:88-90 c

boiling point:172 c (12.7517 mmhg)

density 1.17

appearance: white powder

storage temp. 0-6c

purity: 99%

original: china

grade: pharmaceutical grade

package: disguised package ; foil bag

delivery date: 3-5 work days

certificate: iso 9001, usp, gmp

payment: western union, , t/t, bitcoin

shipping: ems, hkems, eub, etk, fedex, dhl, ups, aramex, etc

policy: re-shipping policy

usage : used for application direct to the skin.

product description

benzocaine hydrochloride is a local anesthetic in the form of hydrochloride salt benzocaine, pharmacological effects with benzocaine, procaine than anesthetic effect is weak. part of the absorption is slow and lasting effect. because they are insoluble in water, can not be used for anesthesia, relieve pain, anti-itching, drugs are usually made of powder or oil paste for the treatment of wound clinical, ulcers, burns, skin abrasions and hemorrhoids.

benzocaine is also known as aminobenzoate, cenuxacin.

benzocaine hcl acts by creating a chemical barrier that prevents the accumulation of sodium, and when the nerve endings are stimulated by pain, sodium accumulates. when the sodium accumulates, the electrical signal will also increase the nerve endings. these are eventually passed to the brain, which interprets the signal as pain.

benzocaine hcl is also known as ethyl aminobenzoate, colorless or white diagonal needle-like crystals or crystalline powders. benzocaine hydrochloride is the hydrochloride form of local anesthesia benzocaine, and benzocaine has the same pharmacological effect and weaker anesthesia compared to procaine. local absorption is slow, sustained effect. because it is insoluble in water, can not be used for anesthesia. can be used for pain and itching.

benzazacaine hydrochloride is usually made into powder or ointment for the treatment of wounds, ulcers, burns, skin abrasions and hemorrhoids.

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CAS:137-58-6

MF:C14H22N2O

MW:234.34

EINECS:205-302-8

Appearance:White crystalline powder

Lidocaine Hydrochloride Description

Lidocaine hydrochloride is chemically designated as acetamide, 2 - (diethylamino)-N-(2, 6-dimethyl) -, monohydrochloride and has a molecular weight of 270.8. The molecular formula is C14H22N2O.HCl. For lidocaine hydrochloride solutions containing epinephrine, which is chemically designated as (-) -3, 4-dihydroxy--[(methylamino) methyl] benzyl alcohol and has the molecular weight of 183 21. Its molecular formula is C9H13NO3. Lidocaine sterile lidocaine hydrochloride with epinephrine hydrochloride solution of lidocaine hydrochloride injections are sterile pyrogen-free solutions, water containing a local anesthetic with or without epinephrine and are administered intravenously injection.Dosage forms listed as xylocaine-MPF indicates a single dose solutions are methyl Araben REE P F (MPF).

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Prilocaine

Synonyms: 2-(propylamino)-o-propionotoluidid; 2-(Propylamino)-o-propionotoluidide; 2-Methyl-alpha-propylaminopropionanilide; Alpha-n-Propyl-amino-2-methylpropionanilide; Alpha-n-propylamino-2-methylpropionanilide; Astra 1512; Astra 1515; Astra1512

Category: Pharmaceutical raw materials

Grade: Medical grade

CAS: 721-50-6

EINECS: 211-957-0

MF: C13H20N2O

MW: 220.31

Assay: 99%

Packing: 1kg/bag, 25kg/drum

Character: Needle-like crystals. Melting point 37-38 C, boiling point 159-162 C (0.133kPa), refractive index (nD20) 1.5299. Its hydrochloride ([1786-81-8]) is a white crystalline powder. Mp 167-168 C. Soluble in water and ethanol, slightly soluble in chloroform. Sour taste bitter, no foul.

Usage: Local anesthetic. The product efficacy Bipuluka due to good local anesthesia with lidocaine similar strength and speed, but the role of longer, less toxic, due to fast metabolism, accumulation is also smaller. Suitable for epidural anesthesia, conduction anesthesia and infiltration anesthesia.

Description

Prilocaine is a local anesthetic of the amino amide type first prepared by Claes Tegner and Nils Lfgren. In its injectable form (trade name Citanest), it is often used in dentistry. It is also often combined with lidocaine as a preparation for dermal anesthesia (lidocaine/prilocaine or EMLA), for treatment of conditions like paresthesia. As it has low cardiac toxicity, it is commonly used for intravenous regional anaesthesia (IVRA).

In some patients, a metabolite of prilocaine may cause the unusual side effect of methemoglobinemia, which may be treated with methylene blue.

Local anesthetic is a substance that causes loss of sensation only to the area to which it is applied without affecting consciousness. Most local anesthetics structures have amino-ester or an amino-amide group which are linked to hydrophilic (secondary or tertiary amine) and to hydrophobic group (aromatics) on the other side.

Local anesthetics, long duration, lower toxicity, chemicals that are also small Suitable for epidural anesthesia, block anesthesia and infiltration anesthesia, etc.

Application

Application It is a kind of local anesthetic drug . The product has better efficacy than procaine and the local anesthesia intensity and speed being similar as lidocaine but with longer duration time and less toxicity as well as smaller accumulation effect . It is suitable for epidural anesthesia , conduction anesthesia and infiltration anesthesia.

Lidocaine and Prilocaine - Clinical Pharmacology

quick detail

product name: benzocaine hcl

other name: benzocaine hydrochloride

cas: 23239-88-5

appearance: white powder

purity: 99%

trademark: pharmlab

original: china

grade: pharmaceutical grade

package: disguised package ; foil bag

delivery date: 3-5 work days

certificate: iso 9001, usp, gmp

payment: western union, , t/t, bitcoin

shipping: ems, hkems, eub, etk, fedex, dhl, ups, aramex, etc

policy: re-shipping policy

mf: c9h11no2.clh

mw: 201.65

mol file : 23239-88-5.mol

usage : used for application direct to the skin.

content: 99-101%

melting point: greater than 208 degrees

standard: usp26

loss on drying: 0.5%

residue on ignition: 0.1%

heavy metals: 10ppm

product description

benzocaine hydrochloride is a local anesthetic in the form of hydrochloride salt benzocaine, pharmacological effects with benzocaine, procaine than anesthetic effect is weak. part of the absorption is slow and lasting effect. because they are insoluble in water, can not be used for anesthesia, relieve pain, anti-itching, drugs are usually made of powder or oil paste for the treatment of wound clinical, ulcers, burns, skin abrasions and hemorrhoids.

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product name: procaine hcl

other name: procaine hydrochloride

cas: 51-05-8

mf: c13h21cln2o2

mw: 272.77

einecs: 200-077-2

product: categories

appearance: white crystals powder

purity: 99%

trademark: pharmlab

original: china

grade: pharmaceutical grade

certificate: iso 9001, usp, gmp

payment: western union, , t/t, bitcoin

shipping: ems, hkems, eub, etk, fedex, dhl, ups, aramex, et

procaine hcl procaine hydrochloride local anesthetic drugs for pain killer cas 51-05-8

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alias:prilocaine

cas:1786-81-8

mf:c13h21cln2o

mw:256.77

einecs:217-244-0

key words:prilocaine , local anesthesia

character:white powder

delivery time:within 24 hours after payment

shipping ways:ems, tnt, fedex, dhl, by air, etc

payment:western union, , bank transfer

export markets:global

trademark:pharmlab

packing:safe ways 99% pass customs

standard:gmp, iso, up, sp,

origin:guangdong, china

production capacity:6000kg/month

product categories: active pharmaceutical ingredients

packing:foil bag or as requirments

onset and duration of action

when used for infiltration injection in dental patients, the time of onset of anesthesia averages less than 2 minutes with an average duration of soft tissue anesthesia of approximately 2 hours.

based on electrical stimulation studies, prilocaine hydrochloride injection, usp, 4% provides a duration of pulpal anesthesia of approximately 10 minutes in maxillary infiltration injections. in clinical studies, this has been found to provide complete anesthesia for procedures lasting an average of 20 minutes.

when used for inferior alveolar nerve block, the time of onset of prilocaine hydrochloride injection, usp, 4% averages less than three minutes with an average duration of soft tissue anesthesia of approximately 21/2 hours.

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product name: aarticaine hcl

other name: aarticaine hydrochloride

cas: 23964-57-0

appearance: white crystals powder

purity: 99%

trademark: pharmlab

original: china

grade: pharmaceutical grade

package: disguised package ; foil bag

delivery date: 3-5 work days

certificate: iso 9001, usp, gmp

payment: western union, , t/t, bitcoin

shipping: ems, hkems, eub, etk, fedex, dhl, ups, aramex, etc

policy: re-shipping policy

m.f.: c13h21cln2o3s

m.w.: 320.8354

what is aarticaine hcl?

aarticaine hcl is a dental amide type local anesthetic. aspirin is used to control pain. like other local anesthetics, arthritis can cause short, completely reversible anesthesia (loss of sensation) during the (dental) procedure.

in dentistry, altexine is used both for infiltration and blockage, and the blocking technique produces the greatest duration of anesthesia. of patients with hypokalemia who are overly stimulated, lidocaine is not very effective, but adeficin is effective.

comparative studies of lidocaine and aldicaine have found that adriptone is more effective in bilocaine in the first molar area after anesthesia in the case of osmotic injection. as with lidocaine, the possibility of successful anesthesia was as high as 3.81 times. however, there is no evidence to support the use of lidocaine for lower alveolar nerve blockers. in addition, despite the successful use of lidocaine for poor dental nerve blockade, it has been shown that aldicaine is superior to the use of supplemental infiltration of persistent pain after lidocaine.

articaine hcl is a dental local anesthetic. it is the most widely used local anesthetic in many european countries and can be used in many countries around the world. the amide structure of aldicaine is similar to that of other local anesthetics, but its molecular structure differs depending on the presence of the thiophene ring rather than the benzene ring. atacaine is special because it contains additional ester groups that are metabolized by the esterase in the blood and tissue.

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product name: levobupivacaine hcl

other name: levobupivacaine hydrochloride

cas: 27262-48-2

appearance: white crystals powder

purity: 99%

trademark: pharmlab

original: china

grade: pharmaceutical grade

package: disguised package ; foil bag

delivery date: 3-5 work days

certificate: iso 9001, usp, gmp

payment: western union, , t/t, bitcoin

shipping: ems, hkems, eub, etk, fedex, dhl, ups, aramex, etc

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mf:c18h29cln2o

levobupivacaine (rinn) is a local anesthetic that is an aminoamide group. it is the s-enantiomer of bupivacaine. it is an amide derivative of azobicaine hydrochloride with an anesthetic properties.

left bupivacaine reversibly binds to voltage-gated sodium channels to regulate ion flux and prevent neuronal impulses from initiating and delivering (stabilizing neuronal membranes), leading to analgesia and anesthesia. compared with racemic bupivacaine, levobupivacaine is associated with less vasodilatation and has a longer duration of action.

zambucaine hydrochloride is a sodium channel blocker for long-acting local anesthetics for epidural anesthesia. bupivacaine is an isomer of bupivacaine, whose efficacy is similar to that of bupivacaine, reducing the risk of cardiotoxicity.

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English name: Ropivacaine mesylate

English Synonyms: (S) -Ropivacaine Mesilate; S-Ropivacaine mesylate

CAS: 854056-07-8

MF: C18H30N2O4S

MW: 370.5068

Appearance White crystalline powder

Assay 99.5%

Trademark: Pharmlab

Origin: China

Description

Razivacaine Mesylate, is a new long-acting amide type local anesthetic, pure isoleine, with anesthesia and analgesic dual role, high concentrations of ropivacaine mesylate (molecular formula C17H26N2O CH4O3S, English name Ropivacaine Mesylate Injection) Resulting in surgical anesthetic effects, lower concentrations can effectively block the sensory nerve transmission and the impact of motor nerve is very small. Its pharmacological properties for the lower cardiac toxicity, sensory block separation is more obvious, there is vasoconstriction, so no need to add adrenaline. Clinical mainly for surgical anesthesia, local anesthesia and acute pain control.

Pharmacological effects

With anesthesia and analgesic dual role, high concentration can produce surgical anesthesia, lower concentrations can effectively block the sensory nerve transmission and the impact of motor nerve is very small. Its pharmacological properties for the lower cardiac toxicity, sensory block separation is more obvious, there is vasoconstriction, so no need to add adrenaline.

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