238821
3,5-Dichloro-2-hydroxybenzenesulfonic acid sodium salt
99%
Synonym(s):
Sodium 3,5-dichloro-2-hydroxybenzenesulfonate
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About This Item
Linear Formula:
Cl2C6H2(OH)SO3Na
CAS Number:
Molecular Weight:
265.05
Beilstein/REAXYS Number:
3640643
EC Number:
MDL number:
UNSPSC Code:
12171500
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assay
99%
SMILES string
[Na+].Oc1c(Cl)cc(Cl)cc1S([O-])(=O)=O
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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J D Artiss et al.
Clinical chemistry, 30(8), 1389-1392 (1984-08-01)
A colorimetric peroxidase-coupled procedure for determination of creatinine in human serum and urine is described. A 30-s sample pre-treatment with bilirubin oxidase eliminates interference from endogenous bilirubin. The 4-aminoantipyrine-2-hydroxy-3,5-dichlorobenzenesulfonate chromogen system of this method is about fourfold more sensitive than
J D Artiss et al.
Clinica chimica acta; international journal of clinical chemistry, 116(3), 301-309 (1981-11-11)
A uricase-peroxidase coupled system, for the determination of uric acid, applied to a CentrifiChem-500 centrifugal fast analyser is described. Relatively large amounts of ascorbic acid, due to the inclusion of an ascorbate oxidase urine diluent, and hemoglobin appear not to
P Fossati et al.
Clinical chemistry, 29(8), 1494-1496 (1983-08-01)
We describe a new colorimetric method for measuring creatinine in serum and urine. Creatinine hydrolysis is catalyzed by creatinine amidohydrolase, and the creatine so produced is assayed in reactions catalyzed sequentially by creatine amidinohydrolase and sarcosine oxidase in a system
J D Artiss et al.
Clinical biochemistry, 16(6), 334-337 (1983-12-01)
A study into the substitution of sodium 2-hydroxy-3,5-dichlorobenzenesulfonate for phenol in the indicator reaction for an automated glucose procedure is presented. Apart from having physical properties that are more conducive to easy handling than phenol, the former material affords considerably
M W McGowan et al.
Clinical chemistry, 29(8), 1513-1517 (1983-08-01)
A procedure for the enzymatic determination of lecithin and sphingomyelin in aqueous solution is described. The phospholipids are first dissolved in chloroform:methanol (2:1 by vol), the solvent is evaporated, and the residue is redissolved in an aqueous zwitterionic detergent solution.
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