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C70908

Sigma-Aldrich

5-Chlorosalicylic acid

98%

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Synonym(s):
5-Chloro-2-hydroxybenzoic acid
Linear Formula:
ClC6H3(OH)CO2H
CAS Number:
Molecular Weight:
172.57
Beilstein/REAXYS Number:
2046665
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

form

powder

mp

171-172 °C (lit.)

SMILES string

OC(=O)c1cc(Cl)ccc1O

InChI

1S/C7H5ClO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9H,(H,10,11)

InChI key

NKBASRXWGAGQDP-UHFFFAOYSA-N

Gene Information

human ... ALB(213)

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This Item
27301247588A79809
5-Chlorosalicylic acid 98%

C70908

5-Chlorosalicylic acid

Salicylic acid meets analytical specification of Ph. Eur., BP, USP, 99.5-100.5% (calc. to the dried substance)

27301

Salicylic acid

Salicylic acid ACS reagent, ≥99.0%

247588

Salicylic acid

5-Aminosalicylic acid 95%

A79809

5-Aminosalicylic acid

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

200

form

powder

form

-

form

-

form

powder with small lumps

mp

171-172 °C (lit.)

mp

158-161 °C (lit.)

mp

158-161 °C (lit.)

mp

275-280 °C (dec.) (lit.)

Gene Information

human ... ALB(213)

Gene Information

human ... ALB(213), PTPN1(5770)

Gene Information

human ... ALB(213), PTPN1(5770)

Gene Information

human ... ALOX5(240), PPARG(5468), PTGS1(5742), PTGS2(5743)

pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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M A Rubio et al.
Archives of microbiology, 145(2), 123-125 (1986-07-01)
The hybrid strain Pseudomonas sp. WR4016 was subcultivated with increasing concentrations of 5-chlorosalicylate (5----10 mM) as sole carbon source over a period of 9 months. At intervals of approximately 3 months derivative strains WR4017, WR4018 and WR4019 were isolated which
Comparative gastric ulcerogenic effects of meseclazone, 5-chlorosalicylic acid and other nonsteroidal anti-inflammatory drugs following acute and repeated oral administration to rats.
W Diamantis et al.
Toxicology and applied pharmacology, 52(3), 454-461 (1980-03-15)
Debarati Ray et al.
Physical chemistry chemical physics : PCCP, 14(35), 12182-12192 (2012-08-08)
The present work demonstrates the effect of biological confinement on the photophysics and dynamics of a bio-active drug molecule viz., 5-chlorosalicylic acid (5ClSA). 5ClSA is a potential candidate exhibiting Excited-State Intramolecular Proton Transfer (ESIPT) reaction and thereby generating the phototautomer
M A Rubio et al.
Archives of microbiology, 145(2), 116-122 (1986-07-01)
Methylsalicylate-grown cells of Pseudomonas sp. WR401 cometabolized 3-, 4- and 5-substituted halosalicylates to the corresponding halocatechols. Further degradation was unproductive due to the presence of high levels of catechol 2,3-dioxygenase. This strain acquired the ability to utilize 3-chlorobenzoate following acquisition
Thai Ha Tran et al.
Chemosphere, 201, 425-431 (2018-03-13)
The manganese oxide birnessite adsorbed and catalyzed the transformation of the anthelminthic drug niclosamide (NIS) into 2-chloro-4-nitroaniline (CNA) and 5-chlorosalicylic acid (CSA) at acidic pH. The adsorption of NIS was fitted using a linear isotherm for all conditions and reaction

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