chemical-categories

 

USP Grade Pharmaceutical Raw Materials 99%Min Idebenone For Cerebral Infarction 58186-27-9

 

Idebenone Basic Info.:

 

Product Name: Idebenone

CAS: 58186-27-9

Chemical name: 6-(10-Hydroxydecyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone

Molecular formula: C19H30O5

Molecular weight: 338.44

Melting point: (52- 55 °C )

Loss on drying: ≤ 0.5%

Relevant impurities(HPLC ): ≤ 0.8%

Content(HPLC ): ≥ 99.5%

Packing specification: 5Kg / tin, 25Kg / tin

Storage: Sealed and stored at room temperature.

Executive standard:Enterprise standard

Appearance: Orange yellow or orange crystalline powder, odorless, flavorless.

Property: This product is orange yellow or orange crystalline powder, soluble in methanol, ethanol, insoluble in water, odorless, flavorless.

Used for cerebral infarction, cerebral hemorrhage and cerebral artery sclerosis associated with depression, such as language barriers and intelligence impairment, etc.

 

Idebenone Introduction:

 

Idebenone is a kind of new drug for treating senile dementia and improving mental symptom. Also, it is a better antioxidant in cosmetics and health care than Coenzyme Q10 and Vitamin.

 

Idebenone is a modified version of coenzyme Q10 (CoQ10), which is absolutely crucial for metabolic function. Without it, the electron respiratory chain breaks and cells cannot produce energy. It is also the only lipid-soluble antioxidant that is synthesized in our bodies. Natural levels of CoQ10 begin to decrease after age 30.

 

CoQ10 would be a perfect supplement for athletes that expend excessive energy or push the anaerobic envelope were it not for one important detail: under hypoxic conditions (like going anaerobic), CoQ10 becomes pro-oxidative and creates a powerful free radical that can damage DNA, mitochondria, and lipid membranes.

 

There is a synthetic variation of CoQ10 called ubiquinol, also known as idebenone. It has been formulated to have all the advantages of CoQ10 without the pro-oxidative drawback.

 

 

Anabolic Steroid Hormones Powder Metribolone Legal Oral Steroids Methyltrienolone 965-93-5 

 

Methyltrienolone Basic Info.

 

Product Name: Methyltrienolone (Steroids)

Synonyms: Metribolone;Methyltrienolone 

CAS: 965-93-5

MF: C19H24O2

MW: 284.39

EINECS: N/A

Assay: 99%

Chemical Properties: Pale Yellow Solid.

Storage temp.: 2-8°C

Product Categories: Steroids;Intermediates & Fine Chemicals;Pharmaceuticals;trenbolone series

Usage: An anabolic steroid.

Quality standard: Enterprise standard

 

Methyltrienolone Description:

 

Methyltrienolone is a steroid compound that is mostly unavailable on the market black or otherwise. The reason for its obscurity is because it is so highly toxic to the liver that even doses of as little as 2 mgs a week have caused jaundice of the liver. Besides its toxicity to the liver, it will also cause sexual dysfunction and can cause other compounds it is stacked with to exaggerate the effects of estrogen in the body. Although this compound is obviously dangerous and not recommended for use by anybody who values their health, it is worth noting that its muscle-building and fat-burning properties are on par with the highest-rated steroids available today.

Character: White to light yellow crystalline powder.

Usage An anabolic steroid. pharmaceutical material, Steroid hormone, Anabolin.

 

Methyltrienolone Applications:

 

1. Metribolone (methyltrienolone aka R1881) is a potent, non-aromatizable androgen that is structurally similar to trenbolone and has been referred to as “oral tren.” Methyltrienolone binds strongly to the androgen receptor (AR) and is a more potent agonist (activator) of the androgen receptor than is DHT. 17a-methyltrienolone is listed at 30,000 times more anabolic than methyltestosterone according to Julius Vida in “Androgens and Anabolic Agents: Chemistry and Pharmacology.” Effective dosages begin at only 25mcg.

 

2. Studies have shown that taking an oral anabolic steroid with food may decrease its bioavailability.630 This is caused by the fat-soluble nature of steroid hormones, which can allow some of the drug to dissolve with undigested dietary fat, reducing its absorption from the gastrointestinal tract. For maximum utilization, methyltrienolone should be taken on an empty stomach.

 

 

High Quality Pharmaceutical Raw Material Conform USP Diethylstilbestrol 56-53-1 / 6898-97-1

 

Diethylstilbestrol Basic Info.:

 

Product Name: Diethylstilbestrol

Synonyms: Stilbestrol;Diethylstilbesterol;Domestrol;Grafestrol;Estrosyn;Fonatol;LABOTEST-BB LT00233101;

CAS: 56-53-1 / 6898-97-1

MF: C18H20O2

MW: 268.35

EINECS: 200-278-5

Assay: 99%

Melting point: 170-172 °C(lit.)

Storage temp.: 0-6°C

Solubility methanol: 0.1 g/mL, clear, faintly yellow

Stability: Isomerizes rapidly in Benzene, Chloroform, and Ether. Keep Shielded from light.

Water Solubility: Practically insoluble

Chemical Properties: White Solid

Product Categories: Miscellaneous Biochemicals;Intermediates & Fine Chemicals;Pharmaceuticals;STILBESTROL;Other APIs

Usage: Mainly used for low disease and estrogen hormone imbalance caused by functional bleeding, amenorrhea, can also be used before induction of labor stillbirth to increase myometrial oxytocin sensitivity.

 

Diethylstilbestrol Description:

 

Diethylstilbestrol (DES, former BAN stilboestrol) is a synthetic nonsteroidal estrogen that was first synthesized in 1938. It is also classified as an endocrine disruptor. Human exposure to DES occurred through diverse sources, such as dietary ingestion from supplemented cattle feed and medical treatment for certain conditions, including breast and prostate cancers.:)

 

From about 1940 to 1971, DES was given to pregnant women in the mistaken belief it would reduce the risk of pregnancy complications and losses.:)

 

In 1971, DES was shown to cause a rare vaginal tumor in girls and women who had been exposed to this drug in utero. The United States Food and Drug Administration subsequently withdrew DES from use in pregnant women. Follow-up studies have indicated that DES also has the potential to cause a variety of significant adverse medical complications during the lifetimes of those exposed.:)

 

The United States National Cancer Institute recommends women born to mothers who took DES undergo special medical exams on a regular basis to screen for complications as a result of the drug. Individuals who were exposed to DES during their mothers' pregnancies are commonly referred to as "DES daughters" and "DES sons".

 

Diethylstilbestrol Application:

 

A synthetic, nonsteroidal estrogen. Recomended solvents are DMSO, DMF and ethanol, even in these solvents do not store in solution for any prolonged period of time.

 

 

98% Pharmaceutical Anabolic Weight Loss Steroids Raw Powder Halodrol-50 Turinadiol 2446-23-3

 

Halodrol Basic Info.:

 

Product Name: Halodrol (Turinadiol)

Chemical Name: Halodrol-50; Turinadiol; Turinabol-oral; 4-Chlorodehydromethyltestosterone; 4-Chlorodehydrone Thyltestosterone;Oral turinabol;4-ChlordehydroMethyl Testosterone

CAS Number: 2446-23-3

Molecular Formula: C20H31CLO2

Molecular Weight: 336.8960

Assay: 99.5%

Appearance: White powder

 

Halodrol Description:

 

Halodrol also known as 4-chloro-17a-methyl-androst-1,4-diene-3b,17b-diol, or HD is an excellent compound for adding lean hard muscles as well as strength gains. Halodrol is good for improved vascularity, dry gains with only a small to no amount of water retention.

 

Halodrol exhibits an extremely high anabolic to androgenic ratio translating into hard and consistent muscle gains with No aromatization. These gains are notably extremely lean and dry in nature, making this a favorite for the pre-contest athlete, or as an anabolic addition to many stacks. Mainly used to increase muscle mass most particularly in the abdomen region and will increase muscle endurance and decrease your recovery time after workouts.

 

Halodrol Application:

 

1. It is common for Halodrol users to see strength and size gains within the first 1-2 weeks.

2. Halodrol provides exactly that, lean, hard, dry gains as well as strength gains.