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15579-17-6

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15579-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15579-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,7 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15579-17:
(7*1)+(6*5)+(5*5)+(4*7)+(3*9)+(2*1)+(1*7)=126
126 % 10 = 6
So 15579-17-6 is a valid CAS Registry Number.

15579-17-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name trithionate(2-)

1.2 Other means of identification

Product number -
Other names trithionate

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:15579-17-6 SDS

15579-17-6Relevant articles and documents

Kinetics and mechanism of the decomposition of tetrathionate ion in alkaline medium

Varga, Denes,Horvath, Attila K.

, p. 7654 - 7661 (2008/10/09)

The kinetics of the alkaline decomposition of tetrathionate has been studied spectrophotometrically in the pH range of 9.2-12.2 using both phosphate/hydrogen phosphate and carbonate/hydrogen carbonate as buffer systems and by adjusting the ionic strength to I = 0.5 M with sodium perchlorate at T = 25.0 ± 0.1°C. Matrix rank analysis of the spectra recorded between 265 and 330 nm shows the presence of three independent absorbing species. Besides tetrathionate, thiosulfate and trithionate are identified as absorbing products of the decomposition, but sulfite and a trace amount of sulfate are also formed during the alkaline degradation process. With pentathionate, sulfoxylic acid (S(OH)2), S2O3OH-, and S3O3OH- as key intermediates, a 10-step kinetic model is proposed with six fitted kinetic parameters to take all the important characteristics of the experimental curves into account. On the basis of the stoichiometric measurements and the model proposed, it is also enlightened that the product distribution of the reaction continuously varies with pH; thus the kinetic traces cannot be evaluated by assuming a single stoichiometry in contrast to recent studies. Buffer dependence of the decomposition is also discussed.

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