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Merck

73341

Sigma-Aldrich

Echinenon

≥95.0% (HPLC), solid

Synonym(e):

β,β-Carotin4-on

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About This Item

Empirische Formel (Hill-System):
C40H54O
CAS-Nummer:
Molekulargewicht:
550.86
Beilstein:
2030114
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352202
PubChem Substanz-ID:
NACRES:
NA.32

Produktbezeichnung

Echinenon, ≥95.0% (HPLC)

Qualitätsniveau

Assay

≥95.0% (HPLC)

Form

solid

λ

in hexane (with 2% dichloromethane)

UV-Absorption

λ: 459 nm±5 nm Amax

Lagertemp.

−20°C

SMILES String

CC(/C=C/C1=C(C)C(CCC1(C)C)=O)=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/C40H54O/c1-30(18-13-20-32(3)23-25-36-34(5)22-15-28-39(36,7)8)16-11-12-17-31(2)19-14-21-33(4)24-26-37-35(6)38(41)27-29-40(37,9)10/h11-14,16-21,23-26H,15,22,27-29H2,1-10H3/b12-11+,18-13+,19-14+,25-23+,26-24+,30-16+,31-17+,32-20+,33-21+

InChIKey

QXNWZXMBUKUYMD-QQGJMDNJSA-N

Allgemeine Beschreibung

Echinenone is a carotenoid with a conjugated carbonyl group. Echinenone (4-keto-β-carotene) is a monoketo compound, is an intermediate between β-carotene and canthaxanthin in animals. It is one of the major carotenoids of Anabaena sp., and also present in Micrococcus roseus. It is located in the thylakoid membrane of Anabaena. The conversion of β-carotene to echinenone is catalysed by CrtO, a β-carotene ketolase.

Anwendung

Echinenone may be used as an external standard for the extraction of carotenoid from plasma samples. It may also been used as an internal standard, added to samples for extraction and quantification.

Biochem./physiol. Wirkung

Echinenone binds to glocobacter rhodopsin and functions as a light harvesting antenna in Gloeobacter violaceous.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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