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Merck

74283

Sigma-Aldrich

(±)-α-Carotene

≥95.0% (HPLC)

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About This Item

Fórmula empírica (notación de Hill):
C40H56
Número de CAS:
Peso molecular:
536.87
Código UNSPSC:
12352202
ID de la sustancia en PubChem:
NACRES:
NA.32

Nivel de calidad

Ensayo

≥95.0% (HPLC)

Formulario

powder

λ

2 % in methylene chloride (in hexane)

Absorción UV

λ: 445-449 nm Amax

temp. de almacenamiento

−20°C

cadena SMILES

CC(/C=C/C1C(C)=CCCC1(C)C)=C\C=C\C(C)=C\C=C\C=C(C)\C=C\C=C(\C=C\C2=C(C)CCCC2(C)C)C

InChI

1S/C40H56/c1-31(19-13-21-33(3)25-27-37-35(5)23-15-29-39(37,7)8)17-11-12-18-32(2)20-14-22-34(4)26-28-38-36(6)24-16-30-40(38,9)10/h11-14,17-23,25-28,37H,15-16,24,29-30H2,1-10H3/b12-11+,19-13+,20-14+,27-25+,28-26+,31-17+,32-18+,33-21+,34-22+

Clave InChI

ANVAOWXLWRTKGA-JLTXGRSLSA-N

Descripción general

α-Carotene is usually associated with β-carotene in many fruits and vegetables and belongs to the carotenoid family. It is found in higher concentrations of orange carrots, pumpkins, sweet potatoes, and apricots.

Acciones bioquímicas o fisiológicas

α-Carotene exhibits provitamin A (retinal/retinol/retinoic acid) activity that is necessary for enhancing ocular health. It also shows anti-oxidant, and anti-cancer activities and promotes the function of the immune system. α-Carotene has been studied as an important factor in reducing the risk of cardiovascular diseases.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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