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ChemicalBook >> CAS DataBase List >>Metandienone

Metandienone

CAS No.
72-63-9
Chemical Name:
Metandienone
Synonyms
DBOL;Metandrostenolone;Danabol;Dianabole;Methandrolone;17beta-Hydroxy-17-methylandrosta-1,4-dien-3-one;(8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13,17-triMethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-3-one;Crein;Abirol;Geabol
CBNumber:
CB0502711
Molecular Formula:
C20H28O2
Molecular Weight:
300.44
MDL Number:
MFCD00003650
MOL File:
72-63-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-27 22:47:56
Product description Number Pack Size Price
Methandienone solution 1.0?mg/mL in 1,2-dimethoxyethane, ampule of 1?mL, certified reference material, Cerilliant? M-912 1mL $108
17β-Hydroxy-17-methylandrosta-1,4-dien-3-one analytical standard 90151 100mg $186
Metandienone ≥98% 21172 1mg $36
Metandienone ≥98% 21172 10mg $153
Metandienone ≥98% 21172 1mg $32
More product size

Metandienone Properties

Melting point 165-166 °C
Boiling point 381.66°C (rough estimate)
Density 1.0597 (rough estimate)
refractive index 1.4800 (estimate)
Flash point -2℃
storage temp. 2-8°C
solubility Acetonitrile: 1 mg/ml; Ethanol: 1 mg/ml; Methanol: 1 mg/ml
form liquid
pka 15.12±0.60(Predicted)
optical activity [α]1.15/D 0.5±0.5° in chloroform
Merck 5951
BRN 2056255
Henry's Law Constant 4.5×103 mol/(m3Pa) at 25℃, HSDB (2015)
Major Application clinical testing
InChI InChI=1/C20H28O2/c1-18-9-6-14(21)12-13(18)4-5-15-16(18)7-10-19(2)17(15)8-11-20(19,3)22/h6,9,12,15-17,22H,4-5,7-8,10-11H2,1-3H3/t15-,16+,17+,18+,19+,20+/s3
InChIKey XWALNWXLMVGSFR-HLXURNFRSA-N
SMILES [C@]12(CCC3=CC(=O)C=C[C@]3(C)[C@]1(CC[C@]1(C)[C@](O)(C)CC[C@@]21[H])[H])[H] |&1:0,9,11,14,16,21,r|
CAS DataBase Reference 72-63-9(CAS DataBase Reference)
FDA UNII COZ1R7EOCC
ATC code A14AA03,D11AE01
NIST Chemistry Reference Methandrostenolone(72-63-9)
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Flame (GHS02)Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS02,GHS07,GHS08
Signal word  Danger
Hazard statements  H225-H332-H360FD
Precautionary statements  P201-P210-P280-P308+P313-P370+P378-P403+P235
Hazard Codes  F,T
Risk Statements  60-61-11-19-38
Safety Statements  53-45
RIDADR  3249
WGK Germany  3
RTECS  BV8000000
8
HazardClass  6.1(b)
PackingGroup  III
HS Code  29329970
Storage Class 3 - Flammable liquids
Hazard Classifications Acute Tox. 4 Inhalation
Flam. Liq. 2
Repr. 1B
Skin Irrit. 2
Hazardous Substances Data 72-63-9(Hazardous Substances Data)
Toxicity LD50 oral in rat: > 1gm/kg
DEA Controlled Substances CSCN: 4000
CSA SCH: Schedule III
NARC: No

Metandienone price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich M-912 Methandienone solution 1.0?mg/mL in 1,2-dimethoxyethane, ampule of 1?mL, certified reference material, Cerilliant? 72-63-9 1mL $108 2026-04-30 Buy
Sigma-Aldrich 90151 17β-Hydroxy-17-methylandrosta-1,4-dien-3-one analytical standard 72-63-9 100mg $186 2026-04-30 Buy
Cayman Chemical 21172 Metandienone ≥98% 72-63-9 1mg $36 2026-04-30 Buy
Cayman Chemical 21172 Metandienone ≥98% 72-63-9 10mg $153 2026-04-30 Buy
Cayman Chemical 21172 Metandienone ≥98% 72-63-9 1mg $32 2024-03-01 Buy
Product number Packaging Price Buy
M-912 1mL $108 Buy
90151 100mg $186 Buy
21172 1mg $36 Buy
21172 10mg $153 Buy
21172 1mg $32 Buy

Metandienone Chemical Properties,Uses,Production

Indications and Usage

Metandienone is a dehydrogenation derivative of methyltestosterone. Its protein assimilating effects are similar to those of testosterone propionate, but its androgen effects are slightly weaker and are about 1/100 those of the latter. This drug can promote protein synthesis, inhibit protein heterogeneity, maintain a positive nitrogen balance, improve appetite, aid muscle growth, and encourage weight gain. It can cause calcium and phosphorous deposition in bone tissue, promote bone mesenchymal cell formation, and increase bone calcification and growth. It can encourage tissue generation and granulation and speed up healing of wounds. It lowers blood cholesterol and improves fat metabolism.
Metandienone is an androgen and anabolic hormone drug. It is suitable for people with insufficient protein synthesis and increased protein decomposition, such as patients with negative nitrogen balance caused by chronic wasting diseases, severe infections, trauma, and burns, as well as malignant tumors, osteoporosis, stunted children, dwarfism, fractures, less healing, and high cholesterol.

Drug Interactions

When Metandienone is used with oxyphenbutazone, the blood concentration of oxyphenbutazone may increase.

Adverse reactions

1. Metandienone’s adverse are identical to those of regular androgen and anabolic steroids. There may be nausea, vomiting, indigestion, diarrhea, and other digestive tract reactions. Long term, high dosage use may lead to bone weight, water-sodium retention, increased blood supply to skin, hypocalcemia, hyperosteogeny, etc. Women may experience slight virilism, with effects including acne, hirsuitism, lowered voice, clitoral hypertrophy, irregular menstruation, etc. 2. Metandienone’s side effects on the liver include jaundice and liver failure. There have been reports of liver cancer and benign hepatocellular adenoma tied to Metandianone use.

Contradictions

1. Do not use this drug if allergic.
2. Do not use if experiencing liver failure.
3. Do not use during pregnancy or if pregnancy may occur during treatment.
4. Do not use if experiencing prostate cancer, kidney disease, hypertension, or prostate hypertrophy.

Warnings and Precautions

1. Monitor liver functions while using Metandienone.
2. Dosage for elderly patients should be reduced accordingly.
3. Consume appropriate amounts of protein, sugar and vitamins during treatment to improve efficacy.

Chemical Properties

White Solid

Originator

Dianabol,Ciba,US,1960

Uses

Anabolic steroid. Androgen. Controlled substance.

Definition

ChEBI: Methandrostenolone is an organic molecular entity.

Manufacturing Process

As described in US Patent 2,929,763, methandrostenolone may be made by a fermentation route. 2 g of sodium nitrate, 1 g of primary potassium orthophosphate, 0.5 g of magnesium sulfate heptahydrate, 0.5 g of potassium chloride, 50 g of glucose and 1 g of Difco yeast extract are dissolved in one liter of tap water, brought to pH 5 by addition of a sodium hydroxide solution and sterilized. The resulting nutrient solution is inoculated with 50 cc of a 4- day-old shaking culture of Didymella lycopersici and shaken for 48 hours at 27°C, whereby the culture becomes well developed.
To two liters of a culture so prepared there is added under sterile conditions a solution of 500 mg of 17α-methyl-testosterone in 15 cc of acetone. Shaking is carried out for 3 days at 27°C, the mycellium then filtered off with suction, washed with water and ethyl acetate and the combined filtrates extracted with ethyl acetate. The extraction residue obtained after evaporation of the solvent is dissolved in a little acetone. On addition of ether, the 1-dehydro-17αmethyl-testosterone is obtained in compact crystals. MP 163° to 164°C.
An alternative synthetic route is described in US Patent 2,900,398 as follows. A suspension of 30 g of 17α-methyl-testosterone and 10 g of selenium dioxide in 600 cc of tertiary amyl alcohol is treated with 60 g of magnesium powder and 6 cc of glacial acetic acid.
The mixture is refluxed for 24 hours with good stirring in an atmosphere of nitrogen, another 10 g of selenium dioxide being added after 10 hours. After some cooling, the suspension is filtered through some Hyflo and washed thoroughly with ethyl acetate. The resulting brown solution is evaporated in vacuo and the residue dissolved in ethyl acetate.
The ethyl acetate solution is then washed with water, dried and evaporated. To remove any selenium still present, the residue is dissolved in 200 cc of methanol and mixed with 100 g of iron powder and 2 g of active carbon. The mixture is heated for 30 minutes with stirring under reflux, then filtered with suction, washed with methanol and the solution evaporated in vacuo. The residue is then chromatographed on 900 g of aluminum oxide. The residues of the evaporated benzene and ether fractions are treated with active carbon in methanol or acetone, evaporated again, and the residue recrystallized from a mixture of acetone and ether. There are obtained 17.5 g of pure 1-dehydro17α-methyl-testosterone which melts at 163° to 164°C.

Therapeutic Function

Androgen, Anabolic

74-83-9
897-06-3
72-63-9
Synthesis of Metandienone from Methyl bromide and Androsta-1,4-diene-3,17-dione

Metandienone Preparation Products And Raw materials

Global( 312)Suppliers
Supplier Tel Email Country ProdList Advantage
Zhejiang J&C Biological Technology Co.,Limited
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Doublewin Biological Technology Co., Ltd
+86-19971437628 doublewin-bella@nandrolonesteroid.com China 97 58
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+8615571922873 15571922873@163.com China 102 58
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View Lastest Price from Metandienone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Methandienone pictures 2026-06-08 Methandienone
72-63-9
$1.00 1KG 99.9% 500KG .GZ HONESTCHEM CO.,LTD
Methandienone pictures 2026-06-08 Methandienone
72-63-9
$1.00 1g 99.8% 1 .GZ HONESTCHEM CO.,LTD
Metandienone / Methandrostenolone / Dianabol pictures 2026-06-08 Metandienone / Methandrostenolone / Dianabol
72-63-9
1kg 99% 1000kg Shaanxi Xianhe Biotech Co., Ltd
1,2-Dimethoxyethane (test Methandienone, 1.0 )mg/mL Dianabol Tablet Metandienone (Dianabol) Tablet Methandrostenolone 1-Dehydro-17alpha-methyltestosterone Dianabol Methandienone 1,4-Androstadien-17a-Methyl-17-ol-3-one-2,4,6a-d3 1,4-Androstadien-17a-Methyl-17-ol-3-one-d3 Methandrostenolone/Dianabol/Methandienone Methandienone solution Methandienone/danabol Androsta-1,4-dien-3-one,17-hydroxy-17-Methyl-, (17b)- Methandione 17-beta-hydroxy-17-alpha-methyl-androsta-4-dien-3-one 17-beta-Hydroxy-17-alpha-methylandrostra-1,4-dien-3-one 17-beta-hydroxy-17-methyl-androsta-4-dien-3-one 17beta-hydroxy-17-methyl-androsta-4-dien-3-one 17-hydroxy-17-methyl-4-dien-3-on(17-beta)-androsta- 17-hydroxy-17-methyl-4-dien-3-on(17beta)-androsta- 17-Hydroxy-17-methylandrosta-1,4-dien-3-one 17-Methyl-17-hydroxy-1,4-androstadi-en-3-one 1-Dehydro-17-methyltestosterone a1-dehydromethyltesterone Abirol Anabolicum Medivet Anabolin Andoredan Androsta-1,4-dien-3-one, 17beta-hydroxy-17alpha-methyl- Androsta-1,4-dien-3-one, 17beta-hydroxy-17-methyl- Androsta-1,4-dien-3-one, 17-hydroxy-17-methyl-, (17beta)- Androsta-1,4-diene-3-one, 17-hydroxy-17-methyl-, (17beta)- Ciba 17309-Ba ciba17309ba ciba17309-ba Compound 17309 compound17309 Crein dehydromethyltesterone Dehydromethyltestosterone delta(1)-17alpha-methyltestosterone delta(sup1)-17-alpha-methyltestosterone delta(Sup1)-17alpha-Methyltestosterone delta’-17-methyltestosterone delta-1,17-alpha-Methyltestosterone delta'-17-Methyltestosterone Encephan Geabol Metanabol Metandienon Metandienonum Metandrostenolon Metastenol Naposim Nerobol Nerobolettes NSC-42722 Protobolin Stenolon Stenolone Sterolon
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