| Identification | More | [Name]
Oestradiol 17-heptanoate | [CAS]
4956-37-0 | [Synonyms]
1,3,5(10)-ESTRATRIEN-3,17BETA-DIOL 17-ENANTHATE
17-BETA-ESTRADIOL 17-ENANTHATE
17-BETA-ESTRADIOL 17-HEPTANOATE
17BETA-ESTRADIOL ENANTHATE
17BETA-ESTRADIOL HEPTANOATE
3,17BETA-DIHYDROXY-1,3,5[10]-ESTRATRIENE 17-ENANTHATE
BETA-ESTRADIOL-17-ENANTHATE
estra-1,3,5(10)-triene-3,17b-diol 17-heptanoate
ESTRADIOL 17-HEPTANOATE
ESTRADIOL ENANTHATE
oestradiol 17-heptanoate
B-estradiol 17-enanthate
estra-1,3,5(10)-triene-3,17beta-diol 17-heptanoate
Estradiol enantate
ESTRADIOL ENANTHATE, MM(CRM STANDARD)
oestradiol enanthate
1,3,5(10)-Estratreine-3,17β-diol 17-enanthate, 3,17β-Dihydroxy-1,3,5(10)-estratriene 17-enanthate, Estradiol 17-heptanoate
Estra-1,3,5(10)-triene-3,17β-diol 17-heptanoate
SQ-16150 | [EINECS(EC#)]
225-599-8 | [Molecular Formula]
C25H36O3 | [MDL Number]
MFCD00056542 | [Molecular Weight]
384.55 | [MOL File]
4956-37-0.mol |
| Chemical Properties | Back Directory | [Melting point ]
94-96° | [Boiling point ]
509.5±50.0 °C(Predicted) | [density ]
1.11±0.1 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
10.25±0.60(Predicted) | [color ]
White to Off-White | [λmax]
286nm(EtOH)(lit.) | [Merck ]
14,3703 | [InChIKey]
RFWTZQAOOLFXAY-MTBKBWMONA-N | [SMILES]
C[C@]12CC[C@]3([H])C4C=CC(O)=CC=4CC[C@@]3([H])[C@]1([H])CC[C@@H]2OC(=O)CCCCCC |&1:1,4,15,17,21,r| | [CAS DataBase Reference]
4956-37-0(CAS DataBase Reference) |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS08 | [Signal word ]
Warning | [Hazard statements ]
H351-H361 | [Precautionary statements ]
P201-P202-P280-P308+P313-P405-P501 | [Hazard Codes ]
Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R40:Limited evidence of a carcinogenic effect. | [Safety Statements ]
S22:Do not breathe dust .
S36:Wear suitable protective clothing . |
| Hazard Information | Back Directory | [Uses]
Estrogen. | [Definition]
ChEBI: Estradiol enanthate is a steroid ester. | [Synthesis]
Step 1, estradiol as raw material, and heptanoyl chloride in the pyridine catalyzed reaction to obtain diheptanoic acid estradiyl ester; Step 2, the diheptanoic acid estradiyl ester in step 1 as raw material, in an alcohol solvent, under the acti |
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J & K SCIENTIFIC LTD.
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Energy Chemical
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www.energy-chemical.com |
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Spectrum Chemical Manufacturing Corp.
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021-021-021-67601398-809-809-809 15221380277 |
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NCE Biomedical Co.,Ltd.
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