Products Categories
CAS No.: | 33765-68-3 |
---|---|
Name: | Oxendolone |
Article Data: | 6 |
Molecular Structure: | |
Formula: | C20H30 O2 |
Molecular Weight: | 302.457 |
Synonyms: | Estr-4-en-3-one,16b-ethyl-17b-hydroxy- (8CI); 16b-Ethyl-17b-hydroxyestr-4-en-3-one; 16b-Ethyl-19-nortestosterone;Oxendolone; TSAA 291 |
Density: | 1.1g/cm3 |
Melting Point: | 152-153℃ |
Boiling Point: | 451.7°Cat760mmHg |
Flash Point: | 192.4°C |
Safety: | Moderately toxic by intraperitoneal route. Mildly toxic by ingestion. Experimental reproductive effects. A steroid. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS. |
PSA: | 37.30000 |
LogP: | 4.12520 |
Chemical Name: Oxendolone
IUPAC NAME: (8R,9S,10R,13S,14S,16S,17S)-16-ethyl-17-hydroxy-13-methyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one ; (9S,14S,17S)-16-ethyl-17-hydroxy-13-methyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one
CAS No.: 33765-68-3
Molecular Formula: C20H30O2
Molecular Weight: 302.45 g/mol
Density: 1.1 g/cm3
Flash Point: 192.4 °C
Boiling Point: 451.7 °C at 760 mmHg
Following is the structure of 16-Ethyl-17-hydroxyester-4-en-3-one (CAS No.33765-68-3):
The chemical synonymous of 16-Ethyl-17-hydroxyester-4-en-3-one (CAS No.33765-68-3) are Oxendolone ; 16b-Ethyl-17b-Hydroxyestr-4-En-3-One ; 16b-Ethyl-19-Nortestosterone ; Estr-4-En-3-One, 16b-Ethyl-17b-Hydroxy- (8ci) ; Estr-4-En-3-One, 16-Ethyl-17-Hydroxy-, (16b,17b)- (9ci) ; Tsaa 291 ; Estr-4-En-3-One ; 16β-Ethyl-17β-Hydroxyestr-4-En-3-One
1. | ims-rat TDLo:150 mg/kg (female 30D pre):REP | YACHDS Yakuri to Chiryo. Pharmacology and Therapeutics. 7 (1979),943. | ||
2. | orl-rat LD50:12,105 mg/kg | YACHDS Yakuri to Chiryo. Pharmacology and Therapeutics. 7 (1979),937. | ||
3. | ipr-rat LD50:5879 mg/kg | YACHDS Yakuri to Chiryo. Pharmacology and Therapeutics. 7 (1979),937. | ||
4. | orl-mus LD50:5480 mg/kg | IYKEDH Iyakuhin Kenkyu. Study of Medical Supplies. 12 (1981),1204. | ||
5. | ipr-mus LD50:2925 mg/kg | YACHDS Yakuri to Chiryo. Pharmacology and Therapeutics. 7 (1979),937. |
Moderately toxic by intraperitoneal route. Mildly toxic by ingestion. Experimental reproductive effects. A steroid. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS.