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Key Documents

52824

Sigma-Aldrich

(9Z)-β-Carotene

≥90.0% (HPLC)

Sinonimo/i:

(9Z)-β-β-Carotene, 9-cis-β-Carotene, Neo-β-carotene U

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About This Item

Formula empirica (notazione di Hill):
C40H56
Numero CAS:
Peso molecolare:
536.87
Beilstein:
3227021
Numero MDL:
Codice UNSPSC:
12352211
ID PubChem:
NACRES:
NA.32

Saggio

≥90.0% (HPLC)

Forma fisica

solid

Tipo di lipide

unsaturated FAs

Temperatura di conservazione

−20°C

Stringa SMILE

CC1=C(\C=C\C(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(C)(C)CCC1

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/h11-14,17-22,25-28H,15-16,23-24,29-30H2,1-10H3/b12-11+,19-13+,20-14+,27-25+,28-26+,31-17+,32-18+,33-21-,34-22+
OENHQHLEOONYIE-BVZAMQQESA-N

Azioni biochim/fisiol

(9Z)-β-Carotene or 9-cis-β-carotene is a 9-cis retinoic acid precursor in intestinal mucosal glands of humans. 9-cis retinoic acid is a ligand for nuclear receptor and retinoid X receptor (RXR). 9-cis-β-carotene participates in gene regulation. It is majorly present in liver. 9-cis-β-Carotene supplementation inhibits the progression of atherosclerosis. 9-cis-β-carotene may restore photoreceptors in retinitis pigmentosa (RP) and retinal dystrophies.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Changes of carotenoids, color, and vitamin A contents during processing of carrot juice.
Chen, B., et al.
Journal of Agricultural and Food Chemistry, 43, 1912-1918 (1995)
Treatment With 9-cis beta-Carotene-Rich Powder in Patients With Retinitis Pigmentosa: A Randomized Crossover Trial
Rotenstreich Y, et al.
JAMA Ophthalmology, 131(8), 985-992 (2013)
Effects of thermal processing on trans-cis-isomerization of β-carotene in carrot juices and carotene-containing preparations.
Marx, M., et al.
Food Chemistry, 83, 609-617 (2003)
W Stahl et al.
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The analysis of beta-carotene and lycopene, the two predominant carotenoids in human serum and tissues, was extended to the level of geometrical (cis-trans) isomers by using an improved reversed-phase HPLC methodology. We separated five geometrical isomers of beta-carotene and seven
Synthetic 9-cis-beta-carotene inhibits photoreceptor degeneration in cultures of eye cups from rpe65rd12 mouse model of retinoid cycle defect
Sher I, et al.
Scientific Reports, 8(1), 6130-6130 (2018)

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