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Merck

32993

Supelco

Canthaxanthin (trans)

analytical standard

Synonym(e):

β-Carotin-4,4′-dion, E 161g

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About This Item

Empirische Formel (Hill-System):
C40H52O2
CAS-Nummer:
Molekulargewicht:
564.84
Beilstein:
1898520
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
85151701
PubChem Substanz-ID:
E-Nummer:
E161g
NACRES:
NA.24

Biologische Quelle

synthetic

Qualitätsniveau

Qualität

analytical standard

Assay

≥95.0%

Form

solid

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Farbe

brown to very dark red-brown

mp (Schmelzpunkt)

201.6-201.7 °C

Anwendung(en)

food and beverages

Format

neat

Lagertemp.

−20°C

SMILES String

CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)C(=O)CCC1(C)C)\C=C\C=C(C)\C=C\C2=C(C)C(=O)CCC2(C)C

InChI

1S/C40H52O2/c1-29(17-13-19-31(3)21-23-35-33(5)37(41)25-27-39(35,7)8)15-11-12-16-30(2)18-14-20-32(4)22-24-36-34(6)38(42)26-28-40(36,9)10/h11-24H,25-28H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,29-15+,30-16+,31-19+,32-20+

InChIKey

FDSDTBUPSURDBL-DKLMTRRASA-N

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Allgemeine Beschreibung

Canthaxanthin, a diketocarotenoid, belongs to the class of carotenoids and is a strong antioxidant found in many living organisms. The potential antioxidant behavior of canthaxanthin is attributed to the presence of conjugated double bonds in its structure. It is responsible for the animal displays of maturity and the scavenging of reactive oxygen species in plant and animal tissues.

Anwendung

Canthaxanthin (trans) may be used as an analytical reference standard for the determination of the analyte in new soil Dietzia sp. and red coral (Corallium rubrum) samples by high-performance liquid chromatography (HPLC) technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Empfohlene Produkte

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

nwg

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Die Dokumentenbibliothek aufrufen

Eric Giraud et al.
Methods in molecular biology (Clifton, N.J.), 892, 173-183 (2012-05-25)
Some aerobic photosynthetic bacteria produce a cocktail of carotenoids, some of them being of a high economic value. A good example is the photosynthetic Bradyrhizobium sp. strain ORS278, which synthesizes, in addition to the photosynthetic carotenoid spirilloxanthin, large amounts of
Hiromi Arima et al.
FEMS microbiology ecology, 79(1), 34-45 (2011-11-10)
The phylogeny of the terrestrial cyanobacterium Nostoc commune and its neighboring Nostoc species was studied using molecular genetic and chemotaxonomic approaches. At least eight genotypes of N. commune were characterized by the differences among 16S rRNA gene sequences and the
Determination of canthaxanthin in the red coral (Corallium rubrum) from Marseille by HPLC combined with UV and MS detection
Cvejic J, et al.
Marine biology, 152(4), 855-862 (2007)
Mark A Scaife et al.
Bioresource technology, 111, 276-281 (2012-02-23)
Canthaxanthin has a substantial commercial market in aquaculture, poultry production, and cosmetic and nutraceutical industries. Commercial production is dominated by chemical synthesis; however, changing consumer demands fuel research into the development of biotechnology processes. Highly productive microbial systems to produce
Johan Lugtenburg et al.
Acta biochimica Polonica, 59(1), 11-16 (2012-03-20)
Carotenoids and their metabolites are essential factors for the maintenance of important life processes such as photosynthesis. Animals cannot synthesize carotenoids de novo, they must obtain them via their food. In order to make intensive animal husbandry possible and maintain

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