Substance
ID:177345
Names and Identifiers
Synonyms
Hexestrol己烷雌酚二羟二苯己烷4,4′-(1,2-二乙基亚乙基)二苯酚六羟春情素
IUPAC name
4-[(3S,4R)-4-(4-hydroxyphenyl)hexan-3-yl]phenol
IUPAC Traditional name
4-[(3S,4R)-4-(4-hydroxyphenyl)hexan-3-yl]phenol
Registration numbers
Beilstein Number
MDL Number
CAS Number
PubChem SID
EC Number
Properties
Safety Information
German water hazard class
2
GHS Signal Word
Danger
GHS Hazard statements
H350
Personal Protective Equipment
Eyeshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
GHS Precautionary statements
P201-P308+P313
Safety Statements
53-45
GHS Pictograms
Respiratory sensitization, category 1
Germ cell mutagenicity, categories 1A,1B,2
Carcinogenicity, categories 1A,1B,2
Reproductive toxicity, categories 1A,1B,2
Specific Target Organ Toxicity – Single exposure, categories 1,2
Specific Target Organ Toxicity – Repeated exposure, categories 1,2
Aspiration Hazard, category 1
European Hazard Symbols
Toxic (T)Risk Statements
45
RTECS
SL0560850
Pharmacology Properties
Gene Information
human ... ESR1(2099)rat ... Esr1(24890)
Product Information
Grade
analytical standard
Purity
≥98%
Molecule Details
Biochem/physiol Actions
The carcinogen hexestrol is a nonsteroidal synthetic estrogen. Metabolic activation of hexestrol to its quinone, which reacts with DNA to form analogous depurinating adducts, may be a primary critical event leading to oncogenic mutations and cancer initiation.
Linkage
己烯雌酚的还原类似物。
The carcinogen hexestrol is a nonsteroidal synthetic estrogen. Metabolic activation of hexestrol to its quinone, which reacts with DNA to form analogous depurinating adducts, may be a primary critical event leading to oncogenic mutations and cancer initiation.
Linkage
己烯雌酚的还原类似物。
Molecular Spectra
No Data Available
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References
No Data Available
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