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16727-30-3

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16727-30-3 Usage

Uses

Malvin is one of anthocyanins that possess potent antioxidant properties.

Definition

ChEBI: An anthocyanin cation that is malvidin carrying two beta-D-glucosyl residues at positions 3 and 5.

General Description

This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG

Check Digit Verification of cas no

The CAS Registry Mumber 16727-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,2 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16727-30:
(7*1)+(6*6)+(5*7)+(4*2)+(3*7)+(2*3)+(1*0)=113
113 % 10 = 3
So 16727-30-3 is a valid CAS Registry Number.

16727-30-3 Well-known Company Product Price

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  • Sigma

  • (72815)  Malvin(chloride)  ≥90% (HPLC)

  • 16727-30-3

  • 72815-1MG-F

  • 809.64CNY

  • Detail

16727-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name malvin

1.2 Other means of identification

Product number -
Other names MALVIDIN-3,5-DIGLUCOSIDE CHLORIDE

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:16727-30-3 SDS

16727-30-3Upstream product

16727-30-3Relevant articles and documents

Thermodynamics and kinetics of flavylium salts: Malvin revisited

Pina, Fernando

, p. 2109 - 2116 (1998)

The pH-dependent structural transformations in aqueous solutions of natural and synthetic flavylium salts are re-examined. The procedure uses Malvin as a reference compound and exploits the different timescales of the kinetic process that take place prior to the equilibration. For each process a kinetic expression was deduced allowing calculation of all the equilibrium constants and most of the rate constants of the system. The equilibrium constants were confirmed by comparison with the data obtained by 1H NMR. Clear evidence for the formation of significant amounts of trans-chalcone in Malvin was obtained.

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