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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
 $193.00
1/EA		 Add To Favorites
45-10810-5G 5 g
 $740.00
1/EA		 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.
RIDADR NONH for all modes of transport
WGK Germany WGK 2
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥96.0% (UV)
mp 137-141 °C
Storage Temp. −20°C
UNSPSC 12352205

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