chemical-categories

Ansion pharma is a factory providing pharmaceutical intermediate and custom synthesis service. 

 

More products infomation, pls contact us: ann.xu@ansionpharma.com; www.ansionpharma.com

Ansion pharma is a factory providing pharmaceutical intermediate and custom synthesis service. 

 

More products infomation, pls contact us: ann.xu@ansionpharma.com; www.ansionpharma.com

Ansion pharma is a factory providing pharmaceutical intermediate and custom synthesis service. 

 

More products infomation, pls contact us: ann.xu@ansionpharma.com; www.ansionpharma.com

 

99% Purity Steroids Arimidex 120511-73-1 Anastrozole For Women Breast Cancer

 

Anastrozole Basic Info.:

 

Product Name: Anastrozole

Synonyms: Anastrozole;Arimidex

CAS No: 120511-73-1

Molecular formula: C17H19N5

Molecular weight: 293.37

Appearance: White powder.

Assay: 99%

Melting point: 81-82°C

Storage temp.: Store at RT

Minimum order: 10g

Quality standard: USP 32 

 

Anastrozole Descriptions:

 

Anastrozole will begin taking it the day they start their cycle, Anastrozole will run it throughout the duration of steroid administration. Anastrozole is also important to point out GP Anastrozole's ability to increase testosterone in the body. Some studies have shown that natural testosterone levels have increases as much as 60% after the use of this substance for 7 days. Because of this, bodybuilders find Anastrozole extremely effective during PCT where as they are trying to elevate natural levels as much as possible in order to avoid a post cycle "crash".

 

Anastrozole Applications:

 

High Purity Anastrozole/Arimidex/CAS No: 120511-73-1

The drug is appropriately used when using substantial amounts of aromatizing steroids, or when one is prone to gynecomastia and using moderate amounts of such steroids. Arimidex does not have the side effects of aminoglutethimide (Cytadren) and can achieve a high degree of estrogen blockade, much moreso than Cytadren. It is possible to reduce estrogen too much with Arimidex, and for this reason blood tests, or less preferably salivary tests, should be taken after the first week of use to determine if the dosing is correct.

 

 

Effective Legal Muscle Building Steroids Hormone Powder Mebolazine 3625-07-8

 

Mebolazine Basic Info.

 

Product Name: Mebolazine

Alias: Mebolazine; Diarethyl; Dimetazin; Dimetina; Dostalon; Roxilon; 2-alpha-Dimethyl-5-alpha-androstan-17-beta-ol-3

CAS No.: 3625-07-8

Molecular Formula: C42H68N2O2

Molecular Weight: 633.011

EINECS: 214-983-0

Density: 1.24

Purity: ≥99%

Appearance: White Powder

Usage: Diamethazine is an C17-alkylated, anabolic-androgenic steroid, that exhibits similar effects to Superdrol (M226010).

 

Mebolazine Description:

 

Mebolazine is really a variant of the Superdrol molecule with almost the exact same features. It is really just two superdrol molecules paired together and those molecules break apart in the body to form two Superdrol molecules.

 

Mebolazine is very similar in effects to Superdrol, but may be slightly milder on the liver, due to the bonding. No one knows where the molecule actually splits, so it is possible that the molecule makes it past the liver and misses the first pass, thus making it less liver stressful. That being said, Mebolazine has just about the same characteristics as superdrol, meaning it will likely be very supressive to natural androgen production and can’t convert to estrogen, making the need to stack it with something “wet” pretty common.

 

Mebolazine should have the same harsh effects on cholesterol and blood pressure as Superdrol, since it is a DHT compound that is very dry. Common side effects will be similar like extreme back pumps, the ability to gain 15-18lbs of dry mass in a 3 week period, aggressive moods and acne.

 

Mebolazine Application:

 

Dymethazine is really a variant of the Superdrol molecule with almost the exact same features. It is really just two superdrol molecules paired together and those molecules break apart in the body to form two Superdrol molecules.

 

Dymethazine is very similar in effects to Superdrol, but may be slightly milder on the liver, due to the bonding. No one knows where the molecule actually splits, so it is possible that the molecule makes it past the liver and misses the first pass, thus making it less liver stressful.

 

That being said, Dymethazine has just about the same characteristics as superdrol, meaning it will likely be very supressive to natural androgen production and can't convert to estrogen, making the need to stack it with something "wet" pretty common.

 

Dymethazine should have the same harsh effects on cholesterol and blood pressure as Superdrol, since it is a DHT compound that is very dry. Common side effects will be similar like extreme back pumps, the ability to gain 15-18lbs of dry mass in a 3 week period, aggressive moods and acne.

 

 

High Purity 99.5% Tetracaine White Fine Powder For Local Anaesthesia 94-24-6

 

Tetracaine Basic Info.:

 

Product Name: Tetracaine

Synonym: Anetain, Amethocaine, Pontocaine,Ametop,Dicaine

CAS: 94-24-6

MF: C15H24N2O2

MW: 264.36

EINECS: 202-316-6

Assay: 99%

Quality Standards: EnterpriseStandard/Pharma Grade

Appearance: White powder

Package: 25kg/Drum

Usage: Tetracaine is a topical local anesthetic for the eyes. Tetracaine works by interfering with entry of sodium ions into nerve cells. This reduces the ability of nerves to generate an impulse and send pain sensations.

 

Tetracaine Description:

 

Tetracaine (INN, also known as amethocaine; trade name Pontocaine. Ametop and Dicaine) is a potent local anesthetic of the ester group. It is mainly used topically in ophthalmology and as an antipruritic, and it has been used in spinal anesthesia. It is on the World Health Organization's List of Essential Medicines, a list of the most important medication needed in a basic health system.

(1) In biomedical research, tetracaine is used to alter the function of calcium release channels (ryanodine receptors) that control the release of calcium from intracellular stores. Tetracaine is an allosteric blocker of channel function. At low concentrations, tetracaine causes an initial inhibition of spontaneous calcium release events, while at high concentrations, tetracaine blocks release completely.

(2) Tetracaine is the T in Tac, a mixture of 5 to 12 per cent tetracaine, 5M(per myriad), a half per mille (0.5‰), or .05 per cent (1 part in 2000) , and 4 or 10 per cent hydrochloride used in ear, nose & throat surgery and in the emergemcy department where numbing of the surface is needed rapidly, especially when children have been injured in the eye, ear, or other sensitive locations.

(3) Tetracaine is synthesized from 4-butylaminobenzoic acid. The ethyl ester is formed through an acid-catalyzed esterification reaction. Base-catalyzed transesterification is achieved by boiling the ethyl ester of 4-butylaminobenzoic acid with excess 2-dimethylaminoethanol in the presence of a small amount of sodium ethoxide.

 

Tetracaine Applications:

 

Tetracaine is used in different parts of the body to cause numbness or loss of feeling in some patients before having a medical test or procedure.

 

 

Human Growth Hormone Active Pharmaceutical Ingredient Gonadorelin 33515-09-2

 

Gonadorelin Basic Info.:

 

Product Name: Gonadorelin

Other Name: LH-RH, human, Gonadoreline

CAS: 33515-09-2

Purity (HPLC): 98.0%min.

Appearance: White powder

Molecular Formula: C59H83N17O17

Molecular Weight: 1302.39

Single Impurity (HPLC): 0.5%max

Amino Acid Composition: ±10% of theoretical

Peptide Content (N%): ≥80.0% 

Water Content(Karl Fischer): ≤8.0%

Acetate Content(HPIC): ≤10.0%

Specific Rotation (20/D): -55.0~-65.0°(c=1 1%HAc)

MS (ESI): Consistent

Mass Balance: 95.0~105.0%

 

Gonadorelin Description:

 

Gonadorelin is another name for gonadotropin-releasing hormone (GnRH). It is a synthetic decapeptide prepared using solid phase peptide synthesis. GnRH is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary.

GnRH is available as gonadorelin hydrochloride(Factrel®)and gonadorelin diacetate tetrahydrate(Cystorelin®)for injectable use. Studies have described it being used via an infusion pump system to induce ovulation in patients with hypothalamic hypogonadism. It is also used in veterinary medicine as a treatment for cattle with cystic ovarian disease.

 

Gonadorelin Application:

 

Gonadorelin is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary. In the pituitary GnRH stimulates synthesis and release of FSH and LH, a process that is controlled by the frequency and amplitude of GnRH pulses, as well as the feedback of androgens and estrogens. The pulsatility of GnRH secretion has been seen in all vertebrates, and it is necessary to ensure a correct reproductive function. Thus a single hormone, GnRH, controls a complex process of follicular growth, ovulation, and corpus luteum maintenance in the female, and spermatogenesis in the male. Its short half life requires infusion pumps for its clinical use.

 

Ansion pharma is a factory providing pharmaceutical intermediate and custom synthesis service. 

 

More products infomation, pls contact us: ann.xu@ansionpharma.com; www.ansionpharma.com

 

Oral Finasteride / Proscar Steroids Powder For Hairloss Treatment 98319-26-7

 

Finasteride Basic Info.

 

Product Name: Finasteride

Synonyms: Finasteride;Proscar;Prostide;

CAS: 98319-26-7

Molecular Formula: C23H36N2O2

Molecular Weight: 372.5441

Assay: 99%

Appearance: White or off-white crystal powder

Density: 1.066g/cm3

Boiling Point: 576.61°C at 760 mmHg

Flash Point: 177.448°C

Vapour Pressure: 0mmHg at 25°C

Usage: It is 5 alpha - reductase inhibitor that can inhibit testosterone to convert into DHT. Also used for the treatment of Hyperplasia of prostate. Finasteride is a 4-- aza-steroid compound which is a specific inhibitor of the metabolism of testosterone within dihydro testosterone become stronger during the cell type-II enzyme 5a-reductase. The enlarged prostate called benign prostatic hyperplasia or prostate depends on the conversion of testosterone to dihydro-testosterone.

 

Finasteride Description:

 

Finasteride is a popular anti-androgen medication manufactured by Merck most commonly known as either Proscar or Propecia. Based on the progesterone skeleton, Finasteride belongs to a class of medications known as 5alpha-reductase inhibitors and as such is used for the treatment revolving around type 2 5-AR based occurrences.

 

This is important for performance enhancers as DHT based anabolic steroids have specific side-effects that may occur that can largely be remedied with the use of a 5-AR inhibitor such as Finasteride. As a type 2 5-AR inhibitor Finasteride was designed for the purpose of treating hair-loss, prostate enlargement, as well as prostate cancer.

 

Finasteride is very common among those who supplement with anabolic steroids yet fear hair-loss but there are important things you need to understand before you consider Finasteride use. As an androgen suppressor Finasteride can seriously inhibit the gains made while on cycle, severely and on that basis it is not highly recommended for on-cycle hair preservation.

 

Finasteride Applications:

 

Propecia (finasteride) is used to treat male pattern baldness (androgenic alopecia) in men. Oral use though will reduce DHT levels systemically, which may adversely affect training and sex drive.

 

It is also used in combination with doxazosin in the treatment of benign prostatic hyperplasia (BPH).] Finasteride is an orally active testosterone Type II 5-alpha reductase inhibitor, inhibiting the enzyme that converts testosterone to dihydrotestosterone (DHT).

Topically (on the scalp itself) it is of some effect in minimizing further hair loss. In combination with Nizoral and spironolactone (which smells awful, by the way) it can actually reverse loss moderately.

 

For use in cycles with testosterone, I don't think it is bad at all. One simply doesn't want less DHT than normal. As the amount of testosterone in the system increases, the amount of finasteride needed to keep levels down to normal increases. I consider 5 mg/day reasonable at the gram per week level, and proportionally less at lower dosages of testosterone.

 

 

Pharmaceutical Grade Reducing Fat Mass Chemicals Sr9011 SR-9011 1379686-29-9

 

SR9011 Basic Info:

 

Product Name: SR9011

Synonyms: 3-(((4-chlorobenzyl)((5-nitrothiophen-2-yl)methyl)amino)methyl)-N-pentylpyrrolidine-1-carboxamide

CAS No: 1379686-29-9

Molucelar Formula: C23H31ClN4O3S

Molucelar Weight: 479.03524

Solubility: DMSO up to 100 mM

 

Sr9011 Description:

 

SR9011 is a trifunctional methacrylate monomer that provides exceptional adhesion to metal substrates.

SR9011 is recommended for use in peroxide cured coatings, sealants, and PVC-based plastisols. Usage levels of 5% to 10% by weight are recommended.

 

SR9011 is a potent and specific synthetic REV-ERB agonist that binds to REV ERB α with an EC50 ~790 nM and REV-ERB-β with EC50 ~560 nM. It also has good in vivo plasma/brain exposure. The nuclear receptors REV-ERB-α and REV-ERB-β play an integral role in regulating the expression of core clock proteins, driving rhythms in activity and metabolism. Administration of SR9011 alters circadian behavior and the circadian pattern of core clock gene expression in the hypothalami of mice. The circadian expression pattern of an array of metabolic genes in the liver, skeletal muscle and adipose tissue was also altered, resulting in increased energy expenditure. Treatment of diet induced obese mice with SR9011 decreased obesity by reducing fat mass and markedly improved dyslipidaemia and hyperglycaemia. These results indicate that synthetic REV-ERB ligands that pharmacologically target the circadian rhythm may be beneficial in the treatment of sleep disorders as well as metabolic diseases.

 

Sr9011 Application:

 

In vitro: SR9011 was used at 5-10 μM concentration in vitro and in cellular assays.

In vivo: IP administration of SR9011 was used at 100 mg/kg once or twice per day for 12-30 days in different mouse models.