29883-16-7

Basic information

• Product Name: Benzeneacetonitrile, a-[(6-O-b-D-glucopyranosyl-b-D-glucopyranosyl)oxy]-, (aS)-
• Synonyms: Amygdalin,L- (8CI); Benzeneacetonitrile, a-[(6-O-b-D-glucopyranosyl-b-D-glucopyranosyl)oxy]-, (S)-;(S)-Amygdalin; L-Amygdalin; Neoamygdalin
• CAS NO: 29883-16-7
• Molecular Formula: C20H27 N O11
• Molecular Weight: 457.434
• Mol File: 29883-16-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 743.3±60.0 °C(Predicted)
• Density: 1.59±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Benzeneacetonitrile, a-[(6-O-b-D-glucopyranosyl-b-D-glucopyranosyl)oxy]-, (aS)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetonitrile, a-[(6-O-b-D-glucopyranosyl-b-D-glucopyranosyl)oxy]-, (aS)-(29883-16-7)
• EPA Substance Registry System: Benzeneacetonitrile, a-[(6-O-b-D-glucopyranosyl-b-D-glucopyranosyl)oxy]-, (aS)-(29883-16-7)

Safety Data

• Hazardous Substances Data: 29883-16-7(Hazardous Substances Data)

Upstream product

• 66427-91-6 C₂₀H₂₉NO₁₂ 
• 29883-15-6 amygdalin 
• 29883-15-6 amygdalin 

Downstream Products

• 29883-15-6 neoamygdalin 
• 61091-11-0 Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-2-((S)-cyano-phenyl-methoxy)-6-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxymethyl)-tetrahydro-pyran-3-yl ester 

Relevant articles and documents

Changes of amygdalin and volatile components of apricot kernels during the ultrasonically-accelerated debitterizing

Ultrasound has been regarded as an efficient novel technique for debitterizing of the apricot kernels, but its influence is severely concerned on the possible epimerization of D-amygdalin to the L-amygdalin, a more potentially toxigenic compound. Consider

Synthesis and Biological Evaluation of Cyanogenic Glycosides

An efficient procedure for the synthesis of cyanogenic glycosides with different carbohydrate units was developed. Amygdalin (3), prunasin (1), sambunigrin (2), and neoamygdalin (21) were prepared according to the elaborated method, and biological tests, including antifungal, antibacterial, and cytotoxic activities, were performed.