trans-β-Apo-8′-carotenal

SIGMA/10810 - ≥96.0% (UV)

Synonym: Apocarotenal

CAS Number: 1107-26-2
Empirical Formula (Hill Notation): C₃₀H₄₀O
Molecular Weight: 416.64
EC Number: 214-171-6
MDL Number: MFCD00042626
Linear Formula: C₃₀H₄₀O
Product Type: Chemical

Catalog Number	PKG Qty.	Price	Quantity


45-10810-1G	1 g	$185.00 1/EAAdd To Favorites		Add To Favorites
45-10810-5G	5 g	$740.00 1/EAAdd To Favorites		Add To Favorites

assay	≥96.0% (UV)
biological source	synthetic
form	powder
InChI	1S/C30H40O/c1-24(13-8-9-14-25(2)16-11-18-27(4)23-31)15-10-17-26(3)20-21-29-28(5)19-12-22-30(29,6)7/h8-11,13-18,20-21,23H,12,19,22H2,1-7H3/b9-8+,15-10+,16-11+,21-20+,24-13+,25-14+,26-17+,27-18+
InChI key	DFMMVLFMMAQXHZ-DOKBYWHISA-N
loss	≤0.5% loss on drying, 20 °C (HV)
mp	137-141 °C
Quality Level	100
SMILES string	[H]C(=O)C(C)=CC=CC(C)=CC=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C
solubility	chloroform: 1 mg/mL, clear to very faintly turbid, intense red-orange
storage temp.	−20°C

Application:	Tackling the challenge of selective analytical clean-up of complex natural extracts: the curious case of chlorophyll removal: This study outlines a methodology for the selective analytical clean-up of complex natural extracts, which can be applied to enhance the purity and stability of trans-β-Apo-8′-carotenal, particularly useful in the context of life science manufacturing and research and development. This approach is crucial for maintaining the integrity of bioactive compounds during synthesis and storage (Bijttebier et al., 2014 ).
Biochem/physiol Actions:	Natural carotenoid that is formed from β-carotene in vivo and is an inducer of cytochrome P450 1A (CYP1A) in rats and in Ah-receptor-responsive mice.
Other Notes:	Internal standard in the detection of citrus carotenoids by reversed-phase HPLC.