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Key Documents

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C70908

Sigma-Aldrich

5-Chlorosalicylic acid

98%

Sinonimo/i:

5-Chloro-2-hydroxybenzoic acid

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About This Item

Formula condensata:
ClC6H3(OH)CO2H
Numero CAS:
321-14-2
Peso molecolare:
172.57
Beilstein:
2046665
Numero CE:
206-283-9
Numero MDL:
MFCD00002457
Codice UNSPSC:
12352100
ID PubChem:
24892929
NACRES:
NA.22

Saggio

98%

Forma fisica

powder

Punto di fusione

171-172 °C (lit.)

Stringa SMILE

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)
NKBASRXWGAGQDP-UHFFFAOYSA-N

Informazioni sul gene

human ... ALB(213)

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Categorie correlate

Pittogrammi

Skull and crossbones
GHS06

Avvertenze

Danger

Indicazioni di pericolo

H301

Classi di pericolo

Acute Tox. 3 Oral

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
STBK7033
STBJ9900
STBJ8323
STBJ4445
STBC8953V

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5-Iodosalicylic acid technical grade

Sigma-Aldrich

I10600

5-Iodosalicylic acid

Niclosamide (anhydrous) European Pharmacopoeia (EP) Reference Standard

N0560000

Niclosamide (anhydrous)

5-Aminosalicylic acid ≥99%

Sigma-Aldrich

A3537

5-Aminosalicylic acid

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
Hamdy A H Aly et al.
Applied and environmental microbiology, 74(12), 3812-3822 (2008-04-29)
Rhodococcus sp. strain HA01, isolated through its ability to utilize dibenzofuran (DBF) as the sole carbon and energy source, was also capable, albeit with low activity, of transforming dibenzo-p-dioxin (DD). This strain could also transform 3-chlorodibenzofuran (3CDBF), mainly by angular
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