54765

γβ-Carotin

≥90% (HPLC)

• Empirische Formel (Hill-System): C₄₀H₅₆
• CAS-Nummer: 472-93-5
• Molekulargewicht: 536.87
• Beilstein: 3226412
• MDL-Nummer: MFCD29037199
• UNSPSC-Code: 12352202
• PubChem Substanz-ID: 329758057
• NACRES: NA.32

Eigenschaften

• Assay: ≥90% (HPLC)
• Form: solid
• Mol-Gew.: 536.87 g/mol
• λ: in hexane (with 2% dichloromethane)
• UV-Absorption: λ: 458-462 nm A_max
• Lagertemp.: −20°C
• SMILES String: CC(/C=C/C1=C(C)CCCC1(C)C)=C\C=C\C(C)=C\C=C\C=C(C)\C=C\C=C(\C=C\C=C(C)\CCC=C(C)C)C
• InChI: 1S/C40H56/c1-32(2)18-13-21-35(5)24-15-26-36(6)25-14-22-33(3)19-11-12-20-34(4)23-16-27-37(7)29-30-39-38(8)28-17-31-40(39,9)10/h11-12,14-16,18-20,22-27,29-30H,13,17,21,28,31H2,1-10H3/b12-11+,22-14+,23-16+,26-15+,30-29+,33-19+,34-20+,35-24+,36-25+,37-27+
• InChIKey: HRQKOYFGHJYEFS-BXOLYSJBSA-N

Beschreibung

Allgemeine Beschreibung

Research area: Cell Signaling

Carotenoids are tetraterpene pigments known for displaying a range of colors such as yellow, orange, red, and purple. They are mostly found in photosynthetic bacteria, certain species of archaea and fungi, algae, plants, and animals. γ-Carotene, characterized by its unsubstituted β-ionone rings, serves as a precursor to retinoids and is referred to as pro-vitamin A.[1]

Biochem./physiol. Wirkung

Metabolite in carotenoid biosynthesis and the biosynthesis of plant secondary metabolites.

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable