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51881

Supelco

9-cis-Astaxanthin

analytical standard

Sinonimo/i:

(3S,3′S, 9-cis)-3,3′-Dihydroxy-β,β-carotene-4,4′-dione

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About This Item

Formula empirica (notazione di Hill):
C40H52O4
Numero CAS:
Peso molecolare:
596.84
Codice UNSPSC:
85151701
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Saggio

≥90.0% (HPLC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Impurezze

≤10% all-trans-Astaxanthin (HPLC)

applicazioni

cleaning products
cosmetics
food and beverages
personal care

Formato

neat

Temperatura di conservazione

−70°C

Descrizione generale

9-cis-Astaxanthin is an isomer of astaxanthin (3,3 -dihydroxy-β,β-carotene-4,4 -dione), belonging to the xanthophyll family of oxygenated derivatives of carotenoids.

Applicazioni


  • Detection and Analysis of Carbamazepine Metabolites: A study by Cui et al. used LC-MS/MS to detect carbamazepine and its metabolites, including 10,11-Dihydro-10-Hydroxycarbamazepine, in blood samples, indicating its utility as a pharmaceutical intermediate in biochemical assays and research on drug metabolism (Cui et al., 2023).

  • Environmental Dynamics of Carbamazepine Metabolites: Research conducted by Malvar et al. focused on the dynamics of carbamazepine and its main metabolites in soil contamination studies, using methods like LC-MS/MS to trace pharmaceutical intermediates, providing insights into environmental biochemistry and pollution studies (Malvar et al., 2020).

  • Serum Analysis for Drug Monitoring: Li et al. developed a solid-phase extraction method coupled with high-performance liquid chromatography to determine levels of carbamazepine and 10-Hydroxycarbamazepine in human serum, showcasing its application in clinical pharmacokinetics and therapeutic drug monitoring (Li et al., 2018).

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Rapid baseline separation of enantiomers and a mesoform of all-trans-astaxanthin, 13-cis-astaxanthin, adonirubin, and adonixanthin in standards and commercial supplements.
Wang C, et al.
Journal of Chromatography A, 1194(2), 172-177 (2008)

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