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GESTONORONE CAPROATE

CAS No.
1253-28-7
Chemical Name:
GESTONORONE CAPROATE
Synonyms
SH 582;ZK 5623;Depostat;SH 80582;SM-80582;NSC 84054;Primostat;Depostat (TN);Gestronol caproate;Gestronol hexanoate
CBNumber:
CB9718151
Molecular Formula:
C26H38O4
Molecular Weight:
414.58
MDL Number:
MFCD00867860
MOL File:
1253-28-7.mol
Last updated:2023-05-04 17:34:32

GESTONORONE CAPROATE Properties

Melting point 123-124°
alpha D +13° (chloroform)
Boiling point 453.43°C (rough estimate)
Density 1.11
refractive index 1.4840 (estimate)
storage temp. Refrigerator
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form Solid
color Off-White to Pale Beige
FDA UNII U38E620NS6

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS08
Signal word  Danger
Hazard statements  H351-H360-H362
Precautionary statements  P201-P202-P281-P308+P313-P405-P501-P201-P260-P263-P264-P270-P308+P313

GESTONORONE CAPROATE price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Usbiological 164282 Gestonorone Capronate 1253-28-7 500mg $460 2021-12-16 Buy
American Custom Chemicals Corporation API0011567 GESTONORONE CAPROATE 95.00% 1253-28-7 5MG $498.89 2021-12-16 Buy
Product number Packaging Price Buy
164282 500mg $460 Buy
API0011567 5MG $498.89 Buy

GESTONORONE CAPROATE Chemical Properties,Uses,Production

Originator

Depostat,Schering AG

Uses

Gestonorone Capronate, is a pro-drug of Gestonorone, which is a steroidal progestin. It has been shown to have accelerated body weight gain and caused the atrophy of the prostate, uterus, and seminal vesicles in rats. It is also an inhibitor of the reductive pathway of Testosterone (T155000) metabolism.

Uses

Gestonorone Caproate, is a pro-drug of Gestonorone, which is a steroidal progestin. It has been shown to have accelerated body weight gain and caused the atrophy of the prostate, uterus, and seminal vesicles in rats. It is also an inhibitor of the reductive pathway of Testosterone (T155000) metabolism.

Definition

ChEBI: Gestonorone caproate is an organic molecular entity.

Manufacturing Process

2 Methods of producing of 17-α-hydroxyl-19-norprogesteron-17-capronate:
1. To a solution of 1.0 g 17-α-hydroxy-19-norprogesteron in 32 ml capronic acid anhydride 1.32 g p-toluesulfonate (1 mole hydrate) were added, and allowed to stand for 3 h at 37°C. To the solution 1.43 ml conc. hydrochloric acid in 143 ml methanol were added and all this also for 1 h was left under N2. Then mixture was washed with water and treated with ether. Ether extract was washed with water, and dried with Na2SO4. After that ether was distilled and residue was recrystallised with isopropyl ether. 1.1 g of 17-α-hydroxyl-19- norprogesteron-17-capronate was obtained, melting point 123°-124°C.
2. 2.0 g 3-methoxy-17α-hydroxy-17β-acetyl-δ2,5(10)-oestradien, 60 ml capronic acid anhydride, 2.6 g p-toluensulfonate and 18.0 g water were mixed and left for 6 h at room temperature. Then solution obtained was treated ether and sodium bicarbonate and washed with water. Etheral solution was dried over sodium sulfate. After distillation of ether 3.1 g 3,17α-dihydroxy- δ3,5-19-norpregnadien-3,17-dicapronate was produced.
To solution of 3.1 g 3,17α-dihydroxy-δ3,5-19-norpregnadien-3,17-dicapronate in 250 ml methanol 2.5 g conc. hydrochloric acid were added and mixture was left for 1 h. Then mixture was filtered and residue was washed. After recrystallisation with isopropyl ether 17-α-hydroxyl-19-norprogesteron-17- capronate was obtained, melting point 121°-123°C.

Therapeutic Function

Progestin

GESTONORONE CAPROATE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 32)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9553 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29474 58
J & K SCIENTIFIC LTD. 010-82848833 400-666-7788 jkinfo@jkchemical.com China 96815 76
BOC Sciences 1-631-485-4226; 16314854226 info@bocsci.com United States 14059 65
Shanghai TaoSu Biochemical Technology Co., Ltd. 021-33632979 info@tsbiochem.com China 8073 58
BOC Sciences 16314854226 info@bocsci.com United States 9926 65
Hubei Yangxin Medical Technology Co., Ltd. 15374522761 3003392093@qq.com China 7851 55
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 13028896684 sales@rrkchem.com China 55672 58
Energy Chemical 021-58432009 400-005-6266 marketing1@energy-chemical.com China 44894 58

View Lastest Price from GESTONORONE CAPROATE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
GESTONORONE CAPROATE USP/EP/BP pictures 2021-06-03 GESTONORONE CAPROATE USP/EP/BP
1253-28-7
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited
GESTONORONE CAPROATE GestonoroneAcetateCaproate Depostat (TN) 17-Hydroxy-19-norpregn-4-ene-3,20-dione hexanoate 17α-Hydroxy-19-norprogesterone caproate 17α-Hydroxy-19-norprogesterone capronate 17β-Acetyl-17-hydroxyestr-4-ene-3-one hexanoate 19-Nor-17α-caproyloxy-4-pregnene-3,20-dione 19-Norpregn-4-ene-3,20-dione 17-caproate 19-Norpregn-4-ene-3,20-dione, 17-[(1-oxohexyl)oxy]- 19-Norpregn-4-ene-3,20-dione, 17-hydroxy-, hexanoate (6CI, 7CI, 8CI) Depostat Gestonorone capronate Gestronol caproate Gestronol hexanoate Hexanoic acid, ester with 17-hydroxy-19-norpregn-4-ene-3,20-dione (8CI) NSC 84054 Primostat SH 582 SH 80582 ZK 5623 SM-80582 GESTONORONE CAPROATE USP/EP/BP inhibit,Inhibitor,Progesterone Receptor,Gestonorone caproate,Gestonorone Capronate,NR3C3 Centhaquin Impurity 42 1253-28-7 Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals, Steroids