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Tamoxifen citrate

Inhibitor of protein kinase C and induces apoptosis in cancer cells | CAS: 54965-24-1 | C32H37NO8 | 563.65 g/mol

$374.25 - $937.38

Chemical Identifiers

CAS 54965-24-1
Molecular Formula C32H37NO8
Molecular Weight (g/mol) 563.65
MDL Number MFCD00058321
InChI Key FQZYTYWMLGAPFJ-OQKDUQJOSA-N
Synonym tamoxifen citrate, istubal, zitazonium, unii-7frv7310n6, i.c.i. 46474 citrate, tamoxifen citrate salt, farmifeno, ginarsan, jenoxifen
PubChem CID 2733525
ChEBI CHEBI:9397
IUPAC Name (2-{4-[(1Z)-1,2-diphenylbut-1-en-1-yl]phenoxy}ethyl)dimethylamine; 2-hydroxypropane-1,2,3-tricarboxylic acid
SMILES OC(=O)CC(O)(CC(O)=O)C(O)=O.CC\C(=C(/C1=CC=CC=C1)C1=CC=C(OCCN(C)C)C=C1)C1=CC=CC=C1
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Products 2
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Catalog Number Mfr. No. Quantity Price Quantity  
AAJ6095503
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Thermo Scientific Chemicals
J6095503
1 g
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AAJ6095506
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Thermo Scientific Chemicals
J6095506
5 g
Each for $937.38
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Description

Description

Tamoxifen citrate is used as an antiestrogen with potent anti-cancer and PKC inhibitory activities. Tamoxifen Citrate functions as an estrogen receptor antagonist in breast tissue. Tamoxifen Citrate is an agonist towards this receptor in tissues of the endometrium. Tamoxifen Citrate inhibits DNA synthesis and transcription by recruiting co-repressors, which stop estrogen from interacting with genes. When combined with PAX2, Tamoxifen Citrate can inhibit the proliferation of ERBB2. It is also a high affinity activator of the GPR30 receptor. Tamoxifen Citrate is an activator of Estrogen Receptor.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Tamoxifen citrate is used as an antiestrogen with potent anti-cancer and PKC inhibitory activities. Tamoxifen Citrate functions as an estrogen receptor antagonist in breast tissue. Tamoxifen Citrate is an agonist towards this receptor in tissues of the endometrium. Tamoxifen Citrate inhibits DNA synthesis and transcription by recruiting co-repressors, which stop estrogen from interacting with genes. When combined with PAX2, Tamoxifen Citrate can inhibit the proliferation of ERBB2. It is also a high affinity activator of the GPR30 receptor. Tamoxifen Citrate is an activator of Estrogen Receptor.

Solubility
Soluble in methanol (50 mg/ml with heat) or ethanol (10 mg/ml with sonication); very slightly soluble in water (0.3 mg/L @ 20°C; the pH is approximately 3.0-3.5), 0.02 N HCl (0.2 mg/ml @ 37°C)4, acetone ,chloroform,and DMSO(100mM)

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature: 2 - 8°C. Keep away from strong oxidizing agents.
Specifications

Chemical Identifiers

54965-24-1
563.65
FQZYTYWMLGAPFJ-OQKDUQJOSA-N
2733525
(2-{4-[(1Z)-1,2-diphenylbut-1-en-1-yl]phenoxy}ethyl)dimethylamine; 2-hydroxypropane-1,2,3-tricarboxylic acid
C32H37NO8
MFCD00058321
tamoxifen citrate, istubal, zitazonium, unii-7frv7310n6, i.c.i. 46474 citrate, tamoxifen citrate salt, farmifeno, ginarsan, jenoxifen
CHEBI:9397
OC(=O)CC(O)(CC(O)=O)C(O)=O.CC\C(=C(/C1=CC=CC=C1)C1=CC=C(OCCN(C)C)C=C1)C1=CC=CC=C1

Specifications

54965-24-1
C32H37NO8
1 g
14,9048
Soluble in methanol (50mg/ml with heat) or ethanol (10mg/ml with sonication); very slightly soluble in water (0.3mg/L @ 20°C; the pH is approximately 3.0-3.5),0.02 N HCl (0.2mg/ml @ 37°C)4,acetone ,chloroform,and DMSO(100mM)
OC(=O)CC(O)(CC(O)=O)C(O)=O.CC\C(=C(/C1=CC=CC=C1)C1=CC=C(OCCN(C)C)C=C1)C1=CC=CC=C1
563.65
CHEBI:9397
Powder
White
MFCD00058321
Hygroscopic; Light sensitive
tamoxifen citrate, istubal, zitazonium, unii-7frv7310n6, i.c.i. 46474 citrate, tamoxifen citrate salt, farmifeno, ginarsan, jenoxifen
FQZYTYWMLGAPFJ-OQKDUQJOSA-N
(2-{4-[(1Z)-1,2-diphenylbut-1-en-1-yl]phenoxy}ethyl)dimethylamine; 2-hydroxypropane-1,2,3-tricarboxylic acid
2733525
563.65
Tamoxifen citrate
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Safety and Handling

Safety and Handling

GHS H Statement
H350-H360-H362-H302
May cause cancer.
May damage fertility or the unborn child.
May cause harm to breast-fed children.
Harmful if swallowed.

P201-P202-P264b-P270-P281-P301+P312-P308+P313-P330-P501c

H302-H350

EINECSNumber : 259-415-2

RTECSNumber : KH2387000

TSCA : No

Recommended Storage : Keep cold

SDS
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RUO – Research Use Only