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Merck

254681

3,5-Dichlorosalicylic acid

97%

Synonym(s):

3,5-Dichloro-2-hydroxybenzoic acid

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25 G

HUF 26,900.00

HUF 26,900.00

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About This Item

Linear Formula:
Cl2C6H2(OH)CO2H
CAS Number:
320-72-9
Molecular Weight:
207.01
EC Number:
206-281-8
MDL number:
MFCD00002442
UNSPSC Code:
12352100
PubChem Substance ID:
24855401
NACRES:
NA.22

Key Documents

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Assay

97%

mp

220-222 °C (lit.)

functional group

carboxylic acid
chloro

SMILES string

OC(=O)c1cc(Cl)cc(Cl)c1O

InChI

1S/C7H4Cl2O3/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2,10H,(H,11,12)

InChI key

CNJGWCQEGROXEE-UHFFFAOYSA-N

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This Item
D124001C70908105910
3,5-Dichlorosalicylic acid 97%

Sigma-Aldrich

254681

3,5-Dichlorosalicylic acid

3,5-Diiodosalicylic acid 99%

Sigma-Aldrich

D124001

3,5-Diiodosalicylic acid

5-Chlorosalicylic acid 98%

Sigma-Aldrich

C70908

5-Chlorosalicylic acid

Salicylic acid ReagentPlus®, ≥99%

Sigma-Aldrich

105910

Salicylic acid

assay

97%

assay

99%

assay

98%

assay

≥99%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

mp

220-222 °C (lit.)

mp

220-230 °C (dec.) (lit.)

mp

171-172 °C (lit.)

mp

158-161 °C (lit.)

functional group

carboxylic acid

functional group

-

functional group

-

functional group

carboxylic acid

General description

3,5-Dichlorosalicylic acid is a bio-active drug and its interaction with a model transport protein bovine serum albumin has been investigated[1]. It is a potential inhibitor of human 20α-hydroxysteroid dehydrogenase[2].

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB0824
STBH2540
STBH8405
STBH3269
STBH1586

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Vincenzo Carbone et al.
Archives of biochemistry and biophysics, 479(1), 82-87 (2008-09-11)
The structure of aldehyde reductase (ALR1) in ternary complex with the coenzyme NADPH and 3,5-dichlorosalicylic acid (DCL), a potent inhibitor of human 20alpha-hydroxysteroid dehydrogenase (AKR1C1), was determined at a resolution of 2.41A. The inhibitor formed a network of hydrogen bonds
Bijan Kumar Paul et al.
Physical chemistry chemical physics : PCCP, 14(25), 8892-8902 (2012-02-07)
The present work demonstrates a detailed characterization of the interaction of a bio-active drug molecule 3,5-dichlorosalicyclic acid (3,5DCSA) with a model transport protein Bovine Serum Albumin (BSA). The drug molecule is a potential candidate exhibiting Excited-State Intramolecular Proton Transfer (ESIPT)
Armelle Tchoumi Neree et al.
Scientific reports, 10(1), 21563-21563 (2020-12-11)
Excess of histamine in gut lumen generates a pronounced gastrointestinal discomfort, which may include diarrhea and peristalsis dysfunctions. Deleterious effects of histamine can be alleviated with antihistamine drugs targeting histamine receptors. However, many antihistamine agents come with various undesirable side
Shaoyang Hu et al.
Chemosphere, 228, 668-675 (2019-05-10)
As the first identified category of disinfection byproducts (DBPs), trihalomethanes (THMs) have received continuous attention. Previous studies have demonstrated that the transformation of aromatic halogenated DBPs during chlor (am)ination resulted in the formation of THMs, which may occur in both
Zhenxuan Zhang et al.
Water research, 170, 115283-115283 (2019-11-19)
Halogenated aromatic disinfection byproducts (DBPs) are a new group of emerging DBPs identified recently. They have been detected in disinfected drinking water, wastewater effluents, recreational water and oil/gas produced water, at concentrations of ng/L to μg/L in general. Previously studies

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