73341

Echinenone

≥95.0% (HPLC), solid

• Synonyme(s) : β,β-Caroten-4-one
• Formule empirique (notation de Hill): C₄₀H₅₄O
• Numéro CAS: 432-68-8
• Poids moléculaire : 550.86
• Numéro Beilstein : 2030114
• Numéro CE : 207-083-4
• Numéro MDL: MFCD06656303
• Code UNSPSC : 12352202
• ID de substance PubChem : 329764812
• Nomenclature NACRES : NA.32

Propriétés

• product name: Echinenone, ≥95.0% (HPLC)
• Niveau de qualité: 100
• Pureté: ≥95.0% (HPLC)
• Forme: solid
• λ: in hexane (with 2% dichloromethane)
• Absorption UV: λ: 459 nm±5 nm A_max
• Température de stockage: −20°C
• Chaîne SMILES: 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+
• Clé InChI: QXNWZXMBUKUYMD-QQGJMDNJSA-N

Description

Description générale

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.

Application

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.

Actions biochimiques/physiologiques

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

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable