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Chlormadinone acetate

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Name

Chlormadinone acetate

EINECS 206-118-0
CAS No. 302-22-7 Density 1.23 g/cm3
PSA 60.44000 LogP 4.75170
Solubility N/A Melting Point 212 °C
Formula C23H29ClO4 Boiling Point 512.5 °C at 760 mmHg
Molecular Weight 404.934 Flash Point 172.5 °C
Transport Information N/A Appearance crystalline solid
Safety 53-22-36/37/39-45 Risk Codes 60-61-40-48
Molecular Structure Molecular Structure of 302-22-7 (Chlormadinone acetate) Hazard Symbols ToxicT
Synonyms

17-(Acetyloxy)-6-chloropregna-4,6-diene-3,20-dione;6-Chloro-17-alpha-acetoxy-4,6-pregnadiene-3,20-dione;6-Chloro-6-dehydro-17alpha-acetoxyprogesterone;Chlordion;Progesterone, 6-chloro-6-dehydro-17-hydroxy-, acetate;

Article Data 26

Chlormadinone acetate Consensus Reports

IARC Cancer Review: Animal Limited Evidence IMEMDT    IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 21 , 1979,p. 365.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) ; Animal Sufficient Evidence IMEMDT    IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 6 , 1974,p. 149.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) .

Chlormadinone acetate Specification

The Chlormadinone acetate with cas registry number of 302-22-7 is a crystalline solid. It is also called 6-Chloro-delta(4,6)-pregnadiene-17a-ol-3,20-dionacetate; 6-Chloro-delta6-dehydro-17a-acetoxyprogesterone. It has an IUPAC name which is [(8R,9S,10R,13S,14S,17R)-17-acetyl-6-chloro-10,13-dimethyl-3-oxo-2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthren-17-yl] acetate. This chemical belongs to the following categories: Intermediates & Fine Chemicals; Pharmaceuticals; Steroids with EINECS registry number of 206-118-0.

The physical properties about this chemical are: (1)ACD/LogP: 3.42; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 3.42; (4)ACD/LogD (pH 7.4): 3.42; (5)ACD/BCF (pH 5.5): 235.55; (6)ACD/BCF (pH 7.4): 235.55; (7)ACD/KOC (pH 5.5): 1735.97; (8)ACD/KOC (pH 7.4): 1735.97; (9)#H bond acceptors: 4; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 3; (12)Index of Refraction: 1.562; (13)Molar Refractivity: 106.62 cm3; (14)Molar Volume: 328.5 cm3; (15)Surface Tension: 46.6 dyne/cm; (16)Density: 1.23 g/cm3; (17)Flash Point: 172.5 °C; (18)Enthalpy of Vaporization: 78.38 kJ/mol; (19)Boiling Point: 512.5 °C at 760 mmHg; (20)Vapour Pressure: 1.28E-10 mmHg at 25°C.

When you are using this chemical, please be cautious about it as the following:
Suspected carcinogen with experimental carcinogenic and tumorigenic data. Moderately toxic by intraperitoneal route. Human maternal and reproductive effects by ingestion, intramuscular, and possibly other routes: ovary, uterus, cervix, vagina, and fallopian tube changes; menstrual cycle changes or disorders; changes in fertility; and other unspecified female effects. A human teratogen that causes developmental abnormalities of the endocrine system in the fetus. Experimental teratogenic and reproductive effects. An oral contraceptive. When heated to decomposition it emits toxic fumes of Cl-.

You can still convert the following datas into molecular structure:
(1)InChI: InChI=1S/C23H29ClO4/c1-13(25)23(28-14(2)26)10-7-18-16-12-20(24)19-11-15(27)5-8-21(19,3)17(16)6-9-22(18,23)4/h11-12,16-18H,5-10H2,1-4H3/t16-,17+,18+,21-,22+,23+/m1/s1;
(2)Smiles: C12=CC(=O)CC[C@@]1([C@@H]1[C@@H](C=C2Cl)[C@H]2[C@@]([C@@](CC2)(OC(=O)C)C(=O)C)(CC1)C)C

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 3gm/kg (3000mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

ENDOCRINE: ADRENAL CORTEX HYPOPLASIA
Kiso to Rinsho. Clinical Report. Vol. 11, Pg. 571, 1977.
mouse LD50 intravenous > 2gm/kg (2000mg/kg) SENSE ORGANS AND SPECIAL SENSES: OTHER: EYE

BEHAVIORAL: ATAXIA

SKIN AND APPENDAGES (SKIN): HAIR: OTHER
Oyo Yakuri. Pharmacometrics. Vol. 15, Pg. 1121, 1978.
mouse LD50 oral > 15gm/kg (15000mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

ENDOCRINE: ADRENAL CORTEX HYPOPLASIA
Kiso to Rinsho. Clinical Report. Vol. 11, Pg. 571, 1977.
mouse LD50 subcutaneous > 10gm/kg (10000mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

ENDOCRINE: ADRENAL CORTEX HYPOPLASIA
Kiso to Rinsho. Clinical Report. Vol. 11, Pg. 571, 1977.
rat LD50 intraperitoneal 5gm/kg (5000mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) Oyo Yakuri. Pharmacometrics. Vol. 4, Pg. 217, 1970.
rat LD50 oral > 10gm/kg (10000mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

ENDOCRINE: ADRENAL CORTEX HYPOPLASIA
Kiso to Rinsho. Clinical Report. Vol. 11, Pg. 571, 1977.
rat LD50 subcutaneous > 10gm/kg (10000mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

ENDOCRINE: ADRENAL CORTEX HYPOPLASIA
Kiso to Rinsho. Clinical Report. Vol. 11, Pg. 571, 1977.

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