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517-21-5

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517-21-5 Usage

General Description

Glyoxal bis(sodium hydrogen sulfite) adduct hydrate is a gyloxal derivative.

Check Digit Verification of cas no

The CAS Registry Mumber 517-21-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 517-21:
(5*5)+(4*1)+(3*7)+(2*2)+(1*1)=55
55 % 10 = 5
So 517-21-5 is a valid CAS Registry Number.
InChI:InChI=1/C2H6O8S2.2Na/c3-1(11(5,6)7)2(4)12(8,9)10;;/h1-4H,(H,5,6,7)(H,8,9,10);;/q;2*+1/p-2

517-21-5 Well-known Company Product Price

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  • Aldrich

  • (50690)  Glyoxalbis(sodiumhydrogensulfite)adducthydrate  technical, ~90% (T)

  • 517-21-5

  • 50690-250G

  • 559.26CNY

  • Detail

517-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name GLYOXAL SODIUM BISULFITE

1.2 Other means of identification

Product number -
Other names glyoxale bis hydrogen sulfite disodium salt

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:517-21-5 SDS

517-21-5Upstream product

517-21-5Relevant articles and documents

5a,10b-dihydrobenzofuro[2,3-b]benzofuran type compounds and related products from p-substituted phenols and glyoxal

Rahmatpour, Ali

, p. 1011 - 1016 (2010)

(Chemical Equation Presented) Condensation reactions of glyoxal with p-substituted phenol derivatives 1a-f have been carried out and the corresponding 5a,10b-dihydrobenzofuro[2,3-b]benzofuran 4a-f type compounds were obtained in good to excellent yields.

Kinetics, Mechanism, and Thermodynamics of Glyoxal-S(IV) Adduct Formation

Olson Terese M.,Hoffmann, Michael R.

, p. 533 - 540 (2007/10/02)

The reversible addition of glyoxal (ethanedial) and S(IV) to form glyoxal monobisulfite (GMBS) was studied spectrophotometrically over the pH range of 0.7-3.3.Far from equilibrium, the rate of GMBS formation is given by d/dt = (k1,appα1) + k2,appα2), where = + + , = + -> + 2->, α1 = ->/, and α2 = 2->/.The apparent rate constants, k1,app = 0.13 M-1 s-1 and k2,app = 2.08E3 M-1 s-1, are pH independent functions of the dehydration equilibrium constants of (CH(OH)2)2 and CHOCH(OH)2, and intrinsic rate constants for the reaction of HSO3- and SO32- with unhydrated and singly hydrated glyoxal.Glyoxal dibisulfite (GDBS) and GMBS were shown to dissociate with a rate given by d/dt = -1 + k"-1KD3 + (k'-2K'a2 + k"-2K"a2KD3)/+>>t + -3 + k-4Ka3/+>>t, where k-1 and k-2 correspond to the release of bisulfite and sulfite, respectively, from unhydrated and hydrated GMBS species; k-3 and k-4 correspond to the release of bisulfite and sulfite from GDBS; KD3 is the dehydration constant for GMBS; K'a2, K"a2, and Ka3 are acid dissociation constants.Stability constants for the formation of GMBS and GDBS were determined to be cK1 = ->/(-) = 2.81E4 M-1 and cK2 = -)2>/(->->) = 1.45E4 M-1 at 25 deg C and μ = 0.2 M.

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