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Allylestrenol

CAS No.
432-60-0
Chemical Name:
Allylestrenol
Synonyms
organon;Turinal;gestanin;gestanol;gestanon;gestanyn;orageston;NSC 37723;ALLYLESTRENOL;allyl-estreno
CBNumber:
CB7739529
Molecular Formula:
C21H32O
Molecular Weight:
300.48
MDL Number:
MFCD00198957
MOL File:
432-60-0.mol
MSDS File:
SDS
Last updated:2024-11-20 11:41:24

Allylestrenol Properties

Melting point 79.5-80°
Boiling point 381.7°C (rough estimate)
Density 0.9914 (rough estimate)
refractive index 1.4800 (estimate)
storage temp. -20°C Freezer
solubility Chloroform (Slightly), Methanol (Slightly)
pka 14.95±0.40(Predicted)
form Solid
color White to Pale Yellow
Merck 14,291
CAS DataBase Reference 432-60-0(CAS DataBase Reference)
FDA UNII I47VB5DZ8O
ATC code G03DC01

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
RTECS  KG7960000

Allylestrenol price More Price(21)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC A554755 Allylestrenol 432-60-0 100mg $50 2021-12-16 Buy
Biosynth Carbosynth FA55289 Allylestrenol 432-60-0 500mg $60 2021-12-16 Buy
Chem-Impex 28191 Allylestrenol,97-102%(assay) 97-102%(assay) 432-60-0 250MG $44.8 2021-12-16 Buy
Chem-Impex 28191 Allylestrenol,97-102%(assay) 97-102%(assay) 432-60-0 10G $817.6 2021-12-16 Buy
Medical Isotopes, Inc. 18468 Allylestrenol 432-60-0 5mg $950 2021-12-16 Buy
Product number Packaging Price Buy
A554755 100mg $50 Buy
FA55289 500mg $60 Buy
28191 250MG $44.8 Buy
28191 10G $817.6 Buy
18468 5mg $950 Buy

Allylestrenol Chemical Properties,Uses,Production

Originator

Alilestrenol ,Terapia

Uses

A synthetic steroid with progestational activity.

Uses

Allylestrenol, is a synthetic sexualsteroid, that is used worldwide in case of endangered pregnancies.

Definition

ChEBI: Allylestrenol is a steroid. It derives from a hydride of an estrane.

Manufacturing Process

To 145 ml of dry methylamine which is cooled to -20°C 1.5 g of lithium cut to small pieces are added. To the solution which is blue in color after 10-20 min, a solution of 3.0 g of oestradiol-3-methylether in 145 ml of absolute ether is added drop wise. Subsequently the reaction mixture is stirred at -10°C for 40 h, after which 50 ml of absolute ethanol are added. Then the methylamine is distilled off at law pressure.
To the remaining solution 50 ml of ether and 50 ml of water are added. The water layer is separated and extracted with ether. The ethereal layer is washed with a 2 N hydrochloric acid solution, subsequently with a saturated sodium bicarbonate solution, and then with water. The ethereal solution is dried and evaporated to dryness. The resulting crude reaction product is dissolved in a mixture of benzene and petroleum ether (1:3) and chromatographed over aluminium oxide. The δ4-17β-hydroxy-oestrene obtained after chromatographic purification has a melting point of 80°-90°C and 95°-100°C after repeated crystallization from petroleum ether.
A solution of 13.2 g of chromium trioxide in a mixture of 120 ml of water and 20 ml of acetic acid is added, with stirring, to a solution of 20 g of δ4-17β- hydroxy-oestrene in 400 ml of benzene. Subsequently the reaction mixture is vigorously stirred at room temperature for 16 h, after which the benzene layer is separated.
The remaining aqueous layer is extracted a few times with benzene and the benzene extracts collected are then added to the separated benzene layer. The benzene extracts are successively washed with dilute sulfuric acid and water and then evaporated to dryness. The residue is crystallized from acetone, and the δ4-17β-oxo-oestrene, melting point 114°-116°C is obtained. To a mixture of 22.4 ml of absolute ether and 1.84 g of magnesium, a mixture of 2.72 ml of allyl bromide and 2.72 ml of absolute ether is added in nitrogen atmosphere. Subsequently a solution of 2 g of δ4-17β-oxo-oestrene in 30 ml of absolute ether is added to this reaction mixture, after which the whole is stirred for 4 h. Then the reaction mixture is poured into acidified ice water. The aqueous mixture is extracted with ether; the ether layer is separated, washed with water, dried over sodium sulfate and evaporated to dryness. The residue is recrystallized from a mixture of ether and petroleum ether, giving δ4-17β-hydroxy-17α-allyl-oestrene, melting point 79.5°-80°C.

Therapeutic Function

Progestin; Antiandrogen

Allylestrenol Preparation Products And Raw materials

Global( 294)Suppliers
Supplier Tel Email Country ProdList Advantage
Wuhan Haorong Biotechnology Co.,ltd
+86-18565342920; +8618565342920 sales@chembj.net China 289 58
Nantong Guangyuan Chemicl Co,Ltd
+undefined17712220823 admin@guyunchem.com China 615 58
Hebei Kangcang new material Technology Co., LTD
+8615713292910 Nancy@kangcang.com.cn China 341 58
BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
+86-18600796368 +86-18600796368 sales@sjar-tech.com China 444 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806 sales@capot.com China 29791 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21634 55
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29884 58
Xiamen AmoyChem Co., Ltd
+86-86-5926051114 +8618959220845 sales@amoychem.com China 6383 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22963 58
Shanghai Longyu Biotechnology Co., Ltd.
+8619521488211 info@longyupharma.com China 2529 58

View Lastest Price from Allylestrenol manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Allylestrenol pictures 2024-11-19 Allylestrenol
432-60-0
US $30.00 / mL 100% 10g TargetMol Chemicals Inc.
Allylestrenol pictures 2024-11-18 Allylestrenol
432-60-0
US $0.00 / g 1g More Than 99% 100kg/Month BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
Allylestrenol pictures 2024-10-25 Allylestrenol
432-60-0
US $0.00-0.00 / KG 1KG 99% 5000 Wuhan Haorong Biotechnology Co.,Ltd
  • Allylestrenol pictures
  • Allylestrenol
    432-60-0
  • US $0.00 / g
  • More Than 99%
  • BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
  • Allylestrenol pictures
  • Allylestrenol
    432-60-0
  • US $0.00-0.00 / KG
  • 99%
  • Wuhan Haorong Biotechnology Co.,Ltd
17-allylestr-4-en-17-beta-ol 17-alpha-allyl-17-beta-hydroxy-4-estrene 17-alpha-allyl-17-beta-hydroxy-delta(sup4)-estren 17-alpha-allyl-3-deoxy-19-nortestosterone 17-alpha-allyl-4-estren-17-beta-ol 17-alpha-allyl-4-oestrene-17-beta-ol 17-alpha-allylestr-4-en-17-beta-ol 17-alpha-allylhydroxy-19-nor-4-androstene 17-hydroxy-17-alpha-allyl-4-estrene 21-methylene-19-nor-17-alpha-preg-4-en-17-o 21-methylene-19-nor-17-alpha-preg-4-en-17-ol ALLYLESTRENOL orageston organon 17-Allyl estr-4-en-17β-ol 17α-Allyl-17β-hydroxy-D4-estren 17α-Allyl-4-oestren-17β-ol 17α-Allylestrenol Estr-4-en-17b-ol, 17-allyl- (6CI, 8CI) Estr-4-en-17-ol, 17-(2-propenyl)-, (17β)- NSC 37723 Turinal 4-ESTREN-17-ALPHA-ALLYL-17-BETA-OL 13-methyl-17-prop-2-enyl-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1h-cyclopenta[a]phenanthren-17-ol 17-alpha-allyloestr-4-en-17-beta-ol 3-deoxy-17-alpha-allyl-19-nortestosterone allyl-estreno allyloestrenol gestanin gestanol gestanon gestanyn 17-allyl-estr-4-en-17-beta-o 1-(1,2,3,4,5,6,7,8,9,10,11,12,14,15-tetradecahydrocyclopenta[a]phenanthren-13-yl)-3-buten-1-ol Estr-4-en-17-ol, 17-(2-propen-1-yl)-, (17β)- Allylestrenol USP/EP/BP AllylestrenolQ: What is Allylestrenol Q: What is the CAS Number of Allylestrenol Q: What is the storage condition of Allylestrenol Q: What are the applications of Allylestrenol USP grade Allyl estrenol API Allylestrenol Estrogen Hormone Raw Powder 4-ESTREN-17α-ALLYL-17β-OL Estr-4-en-17-ol, 17-(2-propenyl)-, (17b)- F9(3-keto-4-aza-5Α-androst-17Β-tert-butyramide) 432-60-0 C21H32O Steroid and Hormone Inhibitors Medicine intermediate