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74283

Sigma-Aldrich

(±)-α-Carotene

≥95.0% (HPLC)

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About This Item

Fórmula empírica (notación de Hill):
C40H56
Número de CAS:
432-70-2
Peso molecular:
536.87
UNSPSC Code:
12352202
PubChem Substance ID:
329765595
NACRES:
NA.32

assay

≥95.0% (HPLC)

form

powder

λ

2 % in methylene chloride (in hexane)

UV absorption

λ: 445-449 nm Amax

storage temp.

−20°C

SMILES string

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+

InChI key

ANVAOWXLWRTKGA-JLTXGRSLSA-N

Categorías relacionadas

General description

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.

Biochem/physiol Actions

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.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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β-Carotene Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1239

β-Carotene

β-Carotene synthetic, ≥93% (UV), powder

Sigma-Aldrich

C9750

β-Carotene

Zeaxanthin analytical standard

Supelco

14681

Zeaxanthin

Lutein Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1699

Lutein

Lycopene ≥98% (HPLC), from tomato

Sigma-Aldrich

SMB00706

Lycopene

Lutein analytical standard

Supelco

07168

Lutein

P Rinaldi et al.
Neurobiology of aging, 24(7), 915-919 (2003-08-21)
In order to assess peripheral levels and activities of a broad spectrum of non-enzymatic and enzymatic antioxidants in elderly subjects with mild cognitive impairment (MCI) and Alzheimer's disease (AD), plasma levels of water-soluble (Vitamin C and uric acid) and of
Michael Englert et al.
Journal of chromatography. A, 1388, 119-125 (2015-03-03)
A carotenoid purification method with dual-mode countercurrent chromatography (CCC) for β-carotene, α-carotene and lutein from a fresh carrot extract was developed. The fluorinated liquid benzotrifluoride (IUPAC name: (trifluoromethyl)benzene) was used as a novel modifier in the non-aqueous ternary solvent system
Carlos E Harjes et al.
Science (New York, N.Y.), 319(5861), 330-333 (2008-01-19)
Dietary vitamin A deficiency causes eye disease in 40 million children each year and places 140 to 250 million at risk for health disorders. Many children in sub-Saharan Africa subsist on maize-based diets. Maize displays considerable natural variation for carotenoid
N J Miller et al.
FEBS letters, 384(3), 240-242 (1996-04-22)
The purpose of this study was to assess the relative antioxidant activities of a range of carotenes and xanthophylls through the extent of their abilities to scavenge the ABTS(.+) radical cation. The results show that the relative abilities of the
A metabolomics approach to unravel the regulating role of phytohormones towards carotenoid metabolism in tomato fruit.
Van Meulebroek, L., et al.
Metabolomics, 11, 667-683 (2015)
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