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10829

Sigma-Aldrich

trans-β-Apo-8′-carotenal

~20% apocarotenal basis (UV-vis), suspension (oily)

Sinônimo(s):

Apocarotenal

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About This Item

Fórmula empírica (Notação de Hill):
C30H40O
Número CAS:
Peso molecular:
416.64
Beilstein:
2064131
Número CE:
Número MDL:
Código UNSPSC:
12352205
ID de substância PubChem:
NACRES:
NA.79

fonte biológica

corn (or maize)

Nível de qualidade

Formulário

suspension (oily)

concentração

~20% (apocarotenal, UV-vis)

cor

black to brown
brown to very dark brown

pf

138-141 °C

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

[H]C(=O)\C(C)=C\C=C\C(C)=C\C=C\C=C(C)\C=C\C=C(C)\C=C\C1=C(C)CCCC1(C)C

InChI

1S/C30H40O/c1-24(13-8-9-14-25(2)16-11-18-27(4)23-31)15-10-17-26(3)20-21-29-28(5)19-12-22-30(29,6)7/h8-11,13-18,20-21,23H,12,19,22H2,1-7H3/b9-8+,15-10+,16-11+,21-20+,24-13+,25-14+,26-17+,27-18+

chave InChI

DFMMVLFMMAQXHZ-DOKBYWHISA-N

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Descrição geral

trans-β-Apo-8′-carotenal is a linear aldehydic carotenoid. It is naturally found in oranges, spinach, grass, tangerines and marigolds and thus, it is directly absorbed from the diet.

Aplicação

trans-β-Apo-8′-carotenal has been used as an internal standard during vitamin E analysis.

Ações bioquímicas/fisiológicas

trans-β-Apo-8′-carotenal is commercially available as a food colorant.
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.

Atenção

solidifies on refrigeration

forma física

Suspension of micronized crystals of apocarotenal dispersed in vegetable oils

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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