A3236

Astaxanthin

≥98% (HPLC)

• Synonym(s): (3S,3′S)-3,3′-Dihydroxy-β,β-carotene-4,4′-dione
• Empirical Formula (Hill Notation): C₄₀H₅₂O₄
• CAS Number: 472-61-7
• Molecular Weight: 596.84
• UNSPSC Code: 12352200
• PubChem Substance ID: 329770821
• EC Number: 207-451-4
• MDL number: MFCD00672621

Properties

• biological source: synthetic
• assay: ≥98% (HPLC)
• form: powder
• shipped in: wet ice
• storage temp.: −20°C
• SMILES string: CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)C([C@@H](O)CC2(C)C)=O)C(C)(C)C[C@H](O)C1=O
• InChI: 1S/C40H52O4/c1-27(17-13-19-29(3)21-23-33-31(5)37(43)35(41)25-39(33,7)8)15-11-12-16-28(2)18-14-20-30(4)22-24-34-32(6)38(44)36(42)26-40(34,9)10/h11-24,35-36,41-42H,25-26H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,27-15+,28-16+,29-19+,30-20+/t35-,36-/m0/s1
• InChI key: MQZIGYBFDRPAKN-UWFIBFSHSA-N

Description

Biochem/physiol Actions

Astaxanthin is a potent carotenoid antioxidant found in marine algae, red yeast and many other plant and animal sources. Animal studies indicate that it reduces blood glucose and ameliorates several parameters of the diabetic metabolic syndrome. It improves blood flow and vascular tone in models of hypertension. In vitro studies indicate that it upregulates connexin 43 and thus, may be chemopreventive against cancer.

Safety Information

• Storage Class: 11 - Combustible Solids
• WGK: WGK 3
• Flash Point (°F): Not applicable
• Flash Point (°C): Not applicable
• PPE (personal protective equipment): Eyeshields, Gloves, type N95 (US)