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Home> CAS DataBase Listed 1 > CAS 10540-29-1
Identification of 10540-29-1
  • Name:
  • Ethanamine,2-[4-[(1Z)-1,2-diphenyl-1-buten-1-yl]phenoxy]-N,N-dimethyl- (Related Reference)
  • EINECS:
  • 234-118-0
  • Synonyms:
  • Ethanamine,2-[4-(1,2-diphenyl-1-butenyl)phenoxy]-N,N-dimethyl-, (Z)-; Ethanamine, 2-[4-[(1Z)-1,2-diphenyl-1-butenyl]phenoxy]-N,N-dimethyl-(9CI); Ethylamine, 2-[p-(1,2-diphenyl-1-butenyl)phenoxy]-N,N-dimethyl-, (Z)-(8CI); (Z)-2-[4-(1,2-Diphenyl-1-butenyl)phenoxy]-N,N-dimethylethanamine; ICI47699; Mammaton; Novaldex; Z-Tamoxifen; trans-Tamoxifen; ? Tamoxifen;
  • InChI:
  • InChI=1S/C26H29NO/c1-4-25(21-11-7-5-8-12-21)26(22-13-9-6-10-14-22)23-15-17-24(18-16-23)28-20-19-27(2)3/h5-18H,4,19-20H2,1-3H3/b26-25-
  • This structure is also available as a 2d Mol file
Safety Data of 10540-29-1 Properties of 10540-29-1
  • Appearance:
  • fine off-white crystalline powder
  • Molecular Weight:
  • 371.51456
  • Density:
  • 1.042 g/cm3
  • Boiling Point:
  • Melting Point:
  • 97-98℃
  • Flash Point:
  • 140 °C
  • Storage Temperature:
  • 2-8°C
  • Refractive index:
  • 1.582
  • Solubility:
  • Insoluble
  • Usage:
  • A nonsteroidal estrogen antagonist of interest in the treatment of some forms of breast cancer. Tamoxifen is a Protein Kinase C inhibitor, and induces apoptosis in human malignant glioma cell lines

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CAS No. 10540-29-1 (Ethanamine,2-[4-[(1Z)-1,2-diphenyl-1-buten-1-yl]phenoxy]-N,N-dimethyl- )

  • CAS No:10540-29-1
  • Molecular Weight: 371.51456
  • Molecular Formula: C26H29NO
Properties Safety and Handling MSDS NMR Spectrum Synthesis Route Precursor and Product
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Precursor and Product
References of Ethanamine,2-[4-[(1Z)-1,2-diphenyl-1-buten-1-yl]phenoxy]-N,N-dimethyl- cas 10540-29-1

Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 575mg/kg (575mg/kg) ? Journal of Antibiotics. Vol. 43, Pg. 1533, 1990.
mouse LD50 oral 2150mg/kg (2150mg/kg) ? Drugs of the Future. Vol. 9, Pg. 186, 1984.
rat LD50 intraperitoneal 700mg/kg (700mg/kg) ? Drugs of the Future. Vol. 9, Pg. 186, 1984.
rat LD50 oral 4100mg/kg (4100mg/kg) ? Drugs of the Future. Vol. 9, Pg. 186, 1984.
women TDLo oral 5600ug/kg/1W- (5.6mg/kg) skin and appendages (skin): breast: other British Medical Journal. Vol. 291, Pg. 1172, 1985.
women TDLo unreported 200ug/kg/D (0.2mg/kg) gastrointestinal: nausea or vomiting blood: leukopenia blood: thrombocytopenia Cancer Treatment Reports. Vol. 60, Pg. 1431, 1976.
women TDLo unreported 5600ug/kg/2W- (5.6mg/kg)

blood: normocytic anemia musculoskeletal: joints

British Journal of Rheumatology. Vol. 33, Pg. 583, 1994.

Safety

Confirmed human carcinogen. Moderately toxic by ingestion and intraperitoneal routes. Human systemic effects by an unspecified route: nausea or vomiting, leukopenia, thrombocytopenia, and skin changes. An experimental teratogen. Other experimental reproductive effects. Human mutation data reported. When heated to decomposition it emits toxic fumes of NOx.
Hazard Codes:
ToxicT
IrritantXi
Risk Statements:
R45:May cause cancer.?
R60:May impair fertility.?
R61:May cause harm to the unborn child.?
R64:May cause harm to breastfed babies.?
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements:
S53:Avoid exposure - obtain special instructions before use.?
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)?
S36:Wear suitable protective clothing.?
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany: 3
RTECS: KR5919600

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