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10829 Sigma

trans-β-Apo-8′-carotenal

~20% apocarotenal basis (UV-vis), suspension (oily)

Synonym: Apocarotenal

  • CAS Number 1107-26-2

  • Empirical Formula (Hill Notation) C30H40O

  • Molecular Weight 416.64

  •  Beilstein Registry Number 2064131

  •  EC Number 214-171-6

  •  MDL number MFCD00042626

  •  PubChem Substance ID 24846659

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Properties

Related Categories Aldehydes, Building Blocks, C13-C60, Carbonyl Compounds, Carotenoid,
InChI Key   DFMMVLFMMAQXHZ-DOKBYWHISA-N
assay   ~20% apocarotenal basis (UV-vis)
form   suspension (oily)
storage temp.   2-8°C

Description

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.

Caution

solidifies on refrigeration

Physical form

Suspension of micronized crystals of apocarotenal dispersed in vegetable oils

Price and Availability

Suggested Laboratory Gloves


Laboratory GlovesThis substance has been tested against several types of hand protection for CE compliance. Click below to find the recommended gloves for handling this product.




All labs need water
Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
2

Documents

Certificate of Analysis

Protocols & Articles

Articles

Retinoic Acid and Gene Expression

All-trans retinoic acid (RA, ATRA) is a pleiotropic activation factor that regulates genes associated with normal vertebrate cellular processes such as cell differentiation, cell proliferation, apopt...
BioFiles 2008, 3.9, 12.
Keywords: Apoptosis, Cancer, Cell proliferation, Cellular processes, Chromatin immunoprecipitation, Condensations, Degradations, Diseases, Gene expression, Hormones, Immunoprecipitation, Ligands, Metabolism, Oxidations, Phosphorylations, Polymerase chain reaction, Sequences, Teratogens, Transcription, Type, Ubiquitinations, Usage, Vitamins

Peer-Reviewed Papers
15

References

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