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29883-16-7

Benzeneacetonitrile, a-[(6-O-b-D-glucopyranosyl-b-D-glucopyranosyl)oxy]-, (aS)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 29883-16-7 Structure

  • Basic information

    1. Product Name: Benzeneacetonitrile, a-[(6-O-b-D-glucopyranosyl-b-D-glucopyranosyl)oxy]-, (aS)-
    2. Synonyms: Amygdalin,L- (8CI); Benzeneacetonitrile, a-[(6-O-b-D-glucopyranosyl-b-D-glucopyranosyl)oxy]-, (S)-;(S)-Amygdalin; L-Amygdalin; Neoamygdalin
    3. CAS NO:29883-16-7
    4. Molecular Formula: C20H27 N O11
    5. Molecular Weight: 457.434
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29883-16-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 743.3±60.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.59±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzeneacetonitrile, a-[(6-O-b-D-glucopyranosyl-b-D-glucopyranosyl)oxy]-, (aS)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzeneacetonitrile, a-[(6-O-b-D-glucopyranosyl-b-D-glucopyranosyl)oxy]-, (aS)-(29883-16-7)
    11. EPA Substance Registry System: Benzeneacetonitrile, a-[(6-O-b-D-glucopyranosyl-b-D-glucopyranosyl)oxy]-, (aS)-(29883-16-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 29883-16-7(Hazardous Substances Data)

29883-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29883-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,8 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29883-16:
(7*2)+(6*9)+(5*8)+(4*8)+(3*3)+(2*1)+(1*6)=157
157 % 10 = 7
So 29883-16-7 is a valid CAS Registry Number.

29883-16-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [O-β-D-glucopyranosyl-(1-6)-β-D-glucopyranosyloxy]benzeneacetonitrile

1.2 Other means of identification

Product number -
Other names (S)-neoamygdalin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:29883-16-7 SDS

29883-16-7Relevant articles and documents

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

Zhang, Ning,Zhang, Qing-An,Yao, Jian-Li,Zhang, Xin-Yun

, (2019)

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

Phenylalanine derived cyanogenic diglucosides from Eucalyptus camphora and their abundances in relation to ontogeny and tissue type

Neilson, Elizabeth H.,Goodger, Jason Q.D.,Motawia, Mohammed Saddik,Bjarnholt, Nanna,Frisch, Tina,Olsen, Carl Erik,Moller, Birger Lindberg,Woodrow, Ian E.

, p. 2325 - 2334 (2011)

The cyanogenic glucoside profile of Eucalyptus camphora was investigated in the course of plant ontogeny. In addition to amygdalin, three phenylalanine-derived cyanogenic diglucosides characterized by unique linkage positions between the two glucose moiet

Synthesis and Biological Evaluation of Cyanogenic Glycosides

Yashunsky, Dmitry V.,Kulakovskaya, Ekaterina V.,Kulakovskaya, Tatiana V.,Zhukova, Olga S.,Kiselevskiy, Mikhail V.,Nifantiev, Nikolay E.

, p. 460 - 474 (2015/12/23)

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.

Study on the Prevention of Racemization of Amygdalin

Takayama, Yuzi,Kawai, Satoshi

, p. 778 - 781 (2007/10/02)

Studies were conducted to find suitable conditions for the prevention of racemization of amygdalin in aqueous solution.Evaluation of racemization was carried out by determination of the ratios of neoamygdalyn and amygdalin using a capillary gas chromatographic technique.Racemization of amygdalin in aqueous solution was accelerated by increases on pH and temperature, but racemization was low below pH 3.0 even with heating.Ascorbic acid is useful as an acidification reagent for the suppression of racemization, and has the added clinical benefit of vitamin C activity.Keywords - amygdalin; isoamygdalin separation; racemization; racemizati on prevention; capillary gas chromatography

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