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Fórmula empírica (notación de Hill):
C40H54O
Número CAS:
Peso molecular:
550.86
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
12352202
EC Number:
207-083-4
MDL number:
Beilstein/REAXYS Number:
2030114
Servicio técnico
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Permítanos ayudarleNombre del producto
Echinenone, ≥95.0% (HPLC)
Quality Segment
assay
≥95.0% (HPLC)
form
solid
λ
in hexane (with 2% dichloromethane)
UV absorption
λ: 459 nm±5 nm Amax
storage temp.
−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+
InChI key
QXNWZXMBUKUYMD-QQGJMDNJSA-N
General description
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.
Biochem/physiol Actions
Echinenone binds to glocobacter rhodopsin and functions as a light harvesting antenna in Gloeobacter violaceous.
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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