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2-Thiophenecarboxylic acid, 3-sulfo-, 2-methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59337-96-1

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59337-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59337-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,3 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59337-96:
(7*5)+(6*9)+(5*3)+(4*3)+(3*7)+(2*9)+(1*6)=161
161 % 10 = 1
So 59337-96-1 is a valid CAS Registry Number.

59337-96-1SDS

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 2-(methoxycarbonyl)thiophene-3-sulfonic acid

1.2 Other means of identification

Product number -
Other names -

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:59337-96-1 SDS

59337-96-1Upstream product

59337-96-1Downstream Products

59337-96-1Relevant academic research and scientific papers

Photophysical and photochemical studies of thifensulfuron-methyl herbicide in aqueous solution

Aziz, Saadia,Dumas, Stéphane,El Azzouzi, Mohammed,Sarakha, Mohamed,Chovelon, Jean-Marc

scheme or table, p. 210 - 218 (2010/10/01)

The photophysical and photochemical studies of a sulfonylurea herbicide, thifensulfuron-methyl (THM), have been investigated in a buffered aqueous solution. In the first part, the influence of pH on the spectroscopic properties was studied. This allowed the determination of the ground and excited state acidity constants, pKa=4 and 4.4, respectively, thus exhibiting the potential existence of a photoinduced protonation in the singlet state. In the second part, the photolysis kinetics was studied at different pH and varying oxygen concentrations, using an HPK 125W lamp and followed up by the identification of photoproducts formed under continuous photo-irradiation. The kinetics results suggest that the photolysis process is faster in acidic (k=3×10-4s-1) than in basic medium (k=9.8×10-5s-1). The photolysis products were identified by high performance liquid chromatography HPLC-DAD, HPLC-MS and HPLC-MS-MS. In order to obtain a better understanding of the photodegradation mechanism, a laser flash photolysis study was performed. By comparing the quenching rate constant (kq=9.64×108mol-1ls-1) obtained from triplet state quenching by molecular oxygen and from the Stern-Volmer relation (kq=0.41×108mol-1ls-1), the role of the singlet state in the photodegradation process was demonstrated. The photoproducts originating from both singlet and triplet excited states have been identified and hypothetical photodegradation pathways of the thifensulfuron-methyl in aqueous solution are proposed.

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