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141539-83-5

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141539-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141539-83-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,3 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 141539-83:
(8*1)+(7*4)+(6*1)+(5*5)+(4*3)+(3*9)+(2*8)+(1*3)=125
125 % 10 = 5
So 141539-83-5 is a valid CAS Registry Number.

141539-83-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Sodium 5-(3,5-bistrifluoromethylphenylazo)-6-hydroxynaphthalene-2-sulfonate

1.2 Other means of identification

Product number -
Other names sodium 1-(3,5-bistrifluoromethylphenylazo)-2-hydroxy-6-naphthalenesulfonate

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:141539-83-5 SDS

141539-83-5Downstream Products

141539-83-5Relevant articles and documents

Thermodynamic Study of the Aggregation of Azo Dyes containing Two Trifluoromethyl Groups in Aqueous Solutions

Hamada, Kunihiro,Yamada, Kei,Mitsuishi, Masaru,Ohira, Manabu,Mesuda, Koyuki

, p. 1601 - 1606 (1995)

The aggregation behaviour of azo dyes containing two trifluoromethyl groups, sodium 5-(3,5-bistrifluoromethylphenylazo)-6-hydroxynaphthalene-2-sulfonate, 1, and disodium 4-(3,5-bistrifluoromethylphenylazo)-3-hydroxynaphthalene-2,7-disulfonate, 3, in aqueous solutions has been investigated by 19F NMR and visible absorption spectroscopy.The visible absorption spectra of the corresponding azo dyes containing two methyl groups, sodium 5-(3,5-dimethylphenylazo)-6-hydroxynaphthalene-2-sulfonate, 2, and disodium 4-(3,5-dimethylphenylazo)-3-hydroxynaphthalene-2,7-disulfonate, 4, in aqueous solutions have also been measured.From the visible absorption spectra, the aggregation number has been estimated to be 2 for all the dyes in the concentration region under examination (1E-5 to 1E-3 mol dm-3) and the aggregation constants have been calculated, the temperature dependence of which led to the determination of the thermodynamic parameters.Consequently, the substituents in the dyes affected entropically the aggregation processes.The aqueous solutions of 1 at concentrations greater than 5E-3 mol dm-3 became gelatinous while those of 2, 3 and 4 did not. 19F NMR spectra have been recorded to elucidate the bahaviour of 1 and 3 at the higher concentrations.The 19F NMR spectra of both dyes consisted of one singlet whose shapes did not change with dye concentration.The fluorine signals exhibited a progressive shift to higher and lower magnetic field with increasing dye concentration for 1 and 3, respectively.From this concentration dependence, the aggregation constants and the differences in the chemical shifts between the dye monomers and aggregates have been estimated.The aggregation constants determined by 19F NMR were in fair agreement with those calculated using visible absorption spectra.Furthermore, the differences in the chemical shifts between the dye nonomers and aggregates have given important information concerning the relative spatial location between a fluorine atom and an adjacent aromatic ring.

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