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Canthaxanthin (trans)

analytical standard

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Synonym(s):
β-Carotin-4,4′-dione, E 161g
Empirical Formula (Hill Notation):
C40H52O2
CAS Number:
514-78-3
Molecular Weight:
564.84
Beilstein:
1898520
EC Number:
208-187-2
MDL number:
MFCD00016364
UNSPSC Code:
85151701
PubChem Substance ID:
329754427
E Number:
E161g
NACRES:
NA.24

biological source

synthetic

Quality Level

100

grade

analytical standard

Assay

≥95.0%

form

solid

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

color

brown to very dark red-brown

mp

201.6-201.7 °C

application(s)

food and beverages

format

neat

storage temp.

−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+

InChI key

FDSDTBUPSURDBL-DKLMTRRASA-N

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General description

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.

Application

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.

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WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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
Qiong Cheng et al.
Methods in molecular biology (Clifton, N.J.), 892, 143-158 (2012-05-25)
Escherichia coli is a non-carotenogenic bacterium that could synthesize farnesyl pyrophosphate precursor through the isoprenoid pathway. Carotenoid production in E. coli requires heterologous expression of carotenoid synthesis genes. The carotenoid synthesis operons are assembled from genes isolated from carotenogenic bacterial
Arno Hueber et al.
Ophthalmic research, 46(2), 103-106 (2011-02-25)
To describe the long-term outcome of canthaxanthin retinopathy. We identified 13 patients with small golden particles near the macular region among a group of 35 patients with known consumption of canthaxanthin somewhen between 1983 and 1988. One long-term follow-up examination
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