ChemicalBook >> CAS DataBase List >>Cyproterone acetate

Cyproterone acetate

CAS No.
427-51-0
Chemical Name:
Cyproterone acetate
Synonyms
CIPROTERONE ACETATE;ANDROCUR;CYPROSTAT;SH-714;nsc-81430;Cyproviron;cyprosteroneacetate;CYPROTERONE ACETATE;CYPROFERONE ACETATE;cyproteron-racetate
CBNumber:
CB7338955
Molecular Formula:
C24H29ClO4
Molecular Weight:
416.94
MDL Number:
MFCD00864671
MOL File:
427-51-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-27 17:00:41
Product description Number Pack Size Price
Cyproterone acetate for peak identification European Pharmacopoeia (EP) Reference Standard Y0001390 15 mg $127
Cyproterone acetate Pharmaceutical Secondary Standard; Certified Reference Material, certified reference material PHR2809 50MG $400
Cyproterone acetate ≥98% C3412 250mg $350
Cyproterone acetate European Pharmacopoeia (EP) Reference Standard C3283000 30 mg $241
Cyproterone acetate British Pharmacopoeia (BP) Reference Standard BP688 100mg $339
More product size

Cyproterone acetate Properties

Melting point 200-201°C
Boiling point 528.8°C (rough estimate)
Density 1.0677 (rough estimate)
refractive index 1.4429 (estimate)
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility Practically insoluble in water, very soluble in methylene chloride, freely soluble in acetone, soluble in methanol, sparingly soluble in anhydrous ethanol.
form Solid
color White to Off-White
λmax 281nm(MeOH)(lit.)
Merck 14,2774
InChIKey UWFYSQMTEOIJJG-KIXORDEXNA-N
SMILES C[C@@]12C(=CC(=O)[C@@H]3C[C@H]13)C(Cl)=C[C@@]1([H])[C@]3([H])CC[C@@](C(=O)C)(OC(=O)C)[C@@]3(C)CC[C@]21[H] |&1:1,6,8,12,14,18,26,30,r|
FDA UNII 4KM2BN5JHF
NCI Dictionary of Cancer Terms cyproterone acetate
NCI Drug Dictionary cyproterone acetate
EPA Substance Registry System 3'H-Cyclopropa[1,2]pregna-1,4,6-triene-3,20-dione, 17-(acetyloxy)-6-chloro-1,2-dihydro-, (1.beta.,2.beta.)- (427-51-0)
UNSPSC Code 41116107
NACRES NA.77

Pharmacokinetic data

Protein binding Approx 96%
Excreted unchanged in urine <1%
Volume of distribution 10-30(L/kg)
Biological half-life 32.1-56.7 / -

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS07,GHS08
Signal word  Warning
Hazard statements  H312+H332-H351
Precautionary statements  P202-P261-P280-P302+P352+P312-P304+P340+P312-P308+P313
PPE Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  Xn,Xi
Risk Statements  20/21/22-40-36/37/38
Safety Statements  22-36-26
WGK Germany  3
RTECS  GZ2230000
HS Code  29372900
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Carc. 2
Hazardous Substances Data 427-51-0(Hazardous Substances Data)
NFPA 704
0
4 0

Cyproterone acetate price More Price(72)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0001390 Cyproterone acetate for peak identification European Pharmacopoeia (EP) Reference Standard 427-51-0 15 mg $127 2026-04-30 Buy
Sigma-Aldrich PHR2809 Cyproterone acetate Pharmaceutical Secondary Standard; Certified Reference Material, certified reference material 427-51-0 50MG $400 2026-04-30 Buy
Sigma-Aldrich C3412 Cyproterone acetate ≥98% 427-51-0 250mg $350 2026-04-30 Buy
Sigma-Aldrich C3283000 Cyproterone acetate European Pharmacopoeia (EP) Reference Standard 427-51-0 30 mg $241 2026-04-30 Buy
Sigma-Aldrich BP688 Cyproterone acetate British Pharmacopoeia (BP) Reference Standard 427-51-0 100mg $339 2026-04-30 Buy
Product number Packaging Price Buy
Y0001390 15 mg $127 Buy
PHR2809 50MG $400 Buy
C3412 250mg $350 Buy
C3283000 30 mg $241 Buy
BP688 100mg $339 Buy

Cyproterone acetate Chemical Properties,Uses,Production

Description

Cyproterone acetate (CPA) is an androgen receptor antagonist. It binds to human androgen receptors (Ki = 14 nM) and inhibits dihydrotestosterone-induced androgen receptor activation in CV-1 cells (IC50 = 26 nM). CPA (30 mg/kg) decreases ventral prostate weight in castrated immature rats. It also suppresses accessory sexual glands and fertility in adult male rats when administered at a dose of 10 mg/kg. CPA (0.3 μM) also induces apoptosis in primary adult female rat hepatocytes. Formulations containing cyproterone acetate have been used in the treatment of androgenization in females.

Chemical Properties

Crystalline Solid

Originator

Androcur ,Schering,W. Germany,1973

Uses

Cyproterone acetate (CPA) has been shown to exert gestagenic and glucocorticoid effects. Because it inhibits the negative diencephalic pituitary testicular feedback system, it lowers luteinizing hormone (LH) and testosterone production and plasma levels. cyproterone acetate is both an anti-androgen and a progestogen. CPA is used in combined birth control pills, in the treatment of androgen-dependent skin and hair conditions such as acne (Combined with estrogen), seborrhea, excessive hair growth, and scalp hair loss, high androgen levels, in transgender hormone therapy, to treat prostate cancer, to reduce sex drive in sex offenders or men with paraphilias or hypersexuality, to treat early puberty, and for other uses. It is used both at low doses and at higher doses.

Indications

Cyproterone acetate is a progestational antiandrogen that blocks androgen receptor binding and suppresses androgen-sensitive tissues. It is available in a topical form in Europe for the treatment of hirsutism.

Definition

ChEBI: Cyproterone acetate is a steroid ester resulting from the formal condensation of the carboxy group of acetic acid with the 17-hydroxy group of cyproterone. It is an antiandrogenic drug which has recently been recognized to promote the occurrence and growth of intracranial meningiomas. It has a role as an androgen antagonist, a progestin and a geroprotector. It is a 20-oxo steroid, a 3-oxo-Delta(4) steroid, a chlorinated steroid, a steroid ester and an acetate ester. It is functionally related to a cyproterone.

Manufacturing Process

2.34 g of 1,2α-methylene-δ4,6-pregnadiene-17α-ol-3,20-dione-17-acetate are dissolved in 18.25 cc of ethylene chloride which contains 844 rng of perbenzoic acid. The solution is stored for 16 hours at +5°C and 7 hours at room temperature. It is then diluted with methylene chloride and, with aqueous ferrous sulfate solution, sodium bicarbonate solution and with water washed until neutral.
The organic phase is dried over sodium sulfate and then concentrated to dryness. 1.62 g of the thus obtained crude 1,2α-methylene-6,7α-oxido-δ4- pregnene-17α-ol-3,20-dione-17-acetate are dissolved in 109 cc of glacial acetic acid. This solution is then saturated at room temperature with hydrogen chloride gas and stored for 20 hours, It is then diluted with methylene chloride and washed with water until neutral.
The organic phase is dried over sodium sulfate and then concentrated to dryness. The thus obtained crude 6-chloro-1α-chloromethyl-δ4,6-pregnadiene17α-ol-3,20-dione-17-acetate is heated to boiling in 20 cc of collidine for 20 minutes under nitrogen. After dilution with ether it is washed with 4 N hydrochloric acid and washed with water until neutral.
After drying over sodium sulfate and concentration to vacuum the remaining residue is subjected to chromatography over silica gel. Using a benzene-ethyl acetate mixture (19:1) there is eluated 900 mg of 6-chloro-1,2α-methyleneδ4,6-pregnadiene-17α-ol-3,20-dione-17-acetate, which upon recrystallization from isopropyl ether melts at 200° to 201°C.

Therapeutic Function

Antiandrogen

Mechanism of action

The mechanism of action of Cyproterone acetate at the molecular level has never been described conclusively. Studies have found that in rat ventral prostate nuclei, CPA interferes with androgen binding to the androgen receptor. It is possible that CPA interferes with the translocation of the androgen receptor from the cytoplasm to the nuclear compartment. At the transcription level, the effects of CPA also include a reduction of androgen-dependent cellular functions, such as a reduction of acid phosphatase, prostate-specific androgen, and androgen-dependent enzymes such as 5-a-reductase[1].

Side effects

Vbreast tenderness and swelling. Tiredness and weakness (fatigue). Depression or mood changes. Hot flushes or sweats. Swelling in parts of the body (fluid build up). Weight changes. Liver changes (you will have regular blood tests to check for this). Shortness of breath.

Metabolism

Cyproterone is metabolised by various pathways including hydroxylation and conjugation; about 35% of a dose is excreted in urine, the remainder being excreted in the bile. The principal metabolite, 15β-hydroxycyproterone, has anti-androgenic activity

References

[1] Schrder F, et al. Cyproterone Acetate-Mechanism of Action and Clinical Effectiveness in Prostate Cancer Treatment. Cancer, 1993; 72: 3810-3815.

Cyproterone acetate Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 464)Suppliers
Supplier Tel Email Country ProdList Advantage
Nanjing Shizhou Biotechnology Co., Ltd
+86-15850508050 sean.lv@synzest.com China 323 58
CHONGQING CHENCHENG PHARMACEUTICAL CO.,LTD.
15923947264 lf19823605252@163.com China 121 58
Hebei Anlijie Biotechnology Co., Ltd
8615502221916 ably@aljbio.com China 144 58
Hebei Zhuanglai Chemical Trading Co Ltd
+86-16264648883 niki@zlchemi.com China 7245 58
Wuhan JiyunZen Tech Co., Ltd.
+86-18062099985 Amyjiyunzen@yeah.net China 672 58
Beijing Cooperate Pharmaceutical Co.,Ltd
010-60279497 sales01@cooperate-pharm.com CHINA 1803 55
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21585 55
Nanjing Finetech Chemical Co., Ltd.
025-85710122 17714198479 sales@fine-chemtech.com CHINA 885 55
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29812 58
Xiamen AmoyChem Co., Ltd
+86-86-5926051114 sales@amoychem.com China 6366 58

View Lastest Price from Cyproterone acetate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Cyproterone acetate pictures 2026-07-31 Cyproterone acetate
427-51-0
1KG 97%-103%; EP 100 KG WUHAN FORTUNA CHEMICAL CO., LTD
Cyproterone acetate pictures 2026-07-27 Cyproterone acetate
427-51-0
$33.00 99.83% 10g TargetMol Chemicals Inc.
Cyproterone acetate pictures 2026-06-30 Cyproterone acetate
427-51-0
1KG 98.0% 10000KGS Shaanxi Dideu New Materials Co. Ltd
cyprosteroneacetate 1,2-alpha-methylene-6-chloro-delta-(sup4,6)-pregnadiene-17-alpha-ol-3,20-dio 1,2-alpha-methylene-6-chloro-delta(sup6)-17-alpha-hydroxyprogesteroneacetat 1,2-alpha-methylene-6-chloro-pregna-4,6-diene-3,20-dione17-alpha-acetate 17-alpha-acetoxy-6-chloro-1-alpha,2-alpha-methylenepregna-4,6-diene-3,20-dio 20-dione,6-chloro-17-hydroxy-1-alpha,2-alpha-methylene-pregna-6-diene-3 6)-pregnadiene-17-alpha-ol-3,20-dione17-2-alpha-methylene-6-chloro-(sup4 6-chlor-delta(sup6)-1,2-alpha-methylen-17-alpha-hydroxyprogesteronacetat 6-chloro-1,2-alpha-methylene-17-alpha-hydroxy-delta(sup6)-progesteroneaceta 6-chloro-1,2-alpha-methylene-6-dehydro-17-alpha-hydroxyprogesteroneacetate 6-chloro-17-hydroxy-1-alpha,2-alpha-methylenepregna-4,6-diene-3,20-dioneacet 6-chloro-delta(sup6)-1,2-alpha-methylene-17-alpha-hydroxyprogesteroneacetat CYPROSTAT CYPROTERONE ACETATE CYPROFERONE ACETATE 6-CHLORO-1BETA,2BETA-DIHYDRO-17-HYDROXY-3'H-CYCLOPROPA[1,2]-PREGNA-1,4,6-TRIENE-3,20-DIONE ACETATE 6-chloro-1b,2b-dihydro-17-hydroxy-3'h-cyclopropa[1,2]pregna-1,4,6-triene-3,20-dione 17-acetate ANDROCUR 4,6-PREGNADIEN-6-CHLORO-1-ALPHA, 2-ALPHA-METHYLENE-17-OL-3,20-DIONE ACETATE cyproterone17-alpha-acetate cyproteron-racetate nsc-81430 Cyproterone D3 Acetate Cyproterone Acetate BP2000,EP2000 6-chloro-1-beta,2-beta-dihydro-17-hydroxy-3'H-cyclopropa[1,2]pregna-1,4,6-triene-3,20-dione 17-acetate Androcur, Cyprostat 3H-Cyclopropa1,2pregna-1,4,6-triene-3,20-dione, 17-(acetyloxy)-6-chloro-1,2-dihydro-, (1.beta.,2.beta.)- 6-Chloro-1α,2α-methylene-3,20-dioxopregna-4,6-dien-17-yl acetate CyproteroneAcetateedmfep5 CyproteroneAcetateEdmf 6-Chloro-1β,2β-dihydro-17-hydroxy-3μH-cyclopropa(1,2)-pregna-1,4,6-triene-3,20-dione acetate Androcurone acetate SH-714 Cyproterone acetate(Androcur) Cyproviron (1β,2β)-17-(acetyloxy)-6-chloro-1,2-dihydro-3'H-cyclopropa[1,2]pregna-1,4,6-triene-3,20-dione Cyproterone acetate for peak identification * Color Pronk (cyproterone) Cyproterone acetate, 98%, an androgen receptor (AR) antagonist Cyproterone acetate CRS Cyproterone acetate for peak identification CRS Cyproterone Acetate > Cyproterone 17-O-acetate 6-Chloro-3,20-dioxo-1β,2β-dihydro-3′H-cyclopropa-[1,2]pregna-1,4,6-trien-17-yl acetate (1aR,5aR,5bS,8R,8aS,9aS,9bS,9cS)-8-Acetyl-4-chloro-8a,9b-dimethyl-2-oxo-1a,2,5a,5b,6,7,8,8a,9,9a,9b,9c-dodecahydro-1H-cyclopropa[a]pentaleno[1,2-h]naphthalen-8-yl acetate Cyproterone acetate USP/EP/BP Cyproterone Acetate-13C,d3 Cyproterone acetate (C3283000) Cyproterone Acetate D3Q: What is Cyproterone Acetate D3 Q: What is the CAS Number of Cyproterone Acetate D3 Q: What is the storage condition of Cyproterone Acetate D3 Q: What are the applications of Cyproterone Acetate D3 Cyproterone acetateQ: What is Cyproterone acetate Q: What is the CAS Number of Cyproterone acetate Q: What is the storage condition of Cyproterone acetate Q: What are the applications of Cyproterone acetate Cyproterone acetate API Cyproterone acetate chloride Cyproterone (+)-bitartrate salt 3'H-Cyclopropa[1,2]pregna-1,4,6-triene-3,20-dione, 17-(acetyloxy)-6-chloro-1,2-dihydro-, (1β,2β)- 4, 6-PREGNADIEN-6-CHLORO-1α, 2α-METHYLENE-17-OL-3, 20-DIONE ACETATE (2aR,3aS,3bS,3cS,5aS,6R,8aS,8bR)-6-acetyl-10-chloro-3b,5a-dimethyl-2-oxo-2,2a,3,3a,3b,3c,4,5,5a,6,7,8,8a,8b-tetradecahydrocyclopenta[a]cyclopropa[g]phenanthren-6-yl acetate Cyproterone acetate, 10 mM in DMSO Cyproterone caetate