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trans-β-Apo-8′-carotenal_Molecular_structure_CAS_1107-26-2)
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trans-β-Apo-8′-carotenal

Catalog No. 10810 Name Sigma Aldrich
CAS Number 1107-26-2 Website http://www.sigmaaldrich.com
M. F. C30H40O Telephone 1-800-521-8956
M. W. 416.638 Fax
Purity ≥96.0% (UV) Email
Storage Chembase ID: 125908

SYNONYMS

IUPAC name
(2E,4E,6E,8E,10E,12E,14E,16E)-2,6,11,15-tetramethyl-17-(2,6,6-trimethylcyclohex-1-en-1-yl)heptadeca-2,4,6,8,10,12,14,16-octaenal
IUPAC Traditional name
apocarotenal
Synonyms
Apocarotenal

DATABASE IDS

EC Number 214-171-6
MDL Number MFCD00042626
CAS Number 1107-26-2
PubChem SID 24846800
Beilstein Number 2064131

PROPERTIES

Empirical Formula (Hill Notation) C30H40O
Loss on Drying ≤0.5% loss on drying, 20 °C (HV)
Purity ≥96.0% (UV)
Melting Point 137-141 °C
Solubility chloroform: soluble1 mg/mL, clear to very faintly turbid, intense red-orange
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature -20°C
German water hazard class 2

DETAILS

Description (English)
Biochem/physiol Actions
Natural carotenoid that is formed from β-carotene in vivo and is an inducer of cytochrome P450 1A (CYP1A) in rats and in Ah-receptor-responsive mice.
Other Notes
Internal standard in the detection of citrus carotenoids by reversed-phase HPLC1.
Description (简体中文)
Biochem/physiol Actions
Natural carotenoid that is formed from β-carotene in vivo and is an inducer of cytochrome P450 1A (CYP1A) in rats and in Ah-receptor-responsive mice.
Other Notes
Internal standard in the detection of citrus carotenoids by reversed-phase HPLC1.

REFERENCES