3,5-Dichlorosalicylic acid

3,5-Dichlorosalicylic acid
  • CAS No.:320-72-9
Other grades of this product :
3,5-Dichlorosalicylic acid Basic information
Product Name:3,5-Dichlorosalicylic acid
Synonyms:3,5-DICHLOROSSALICYLICACID;3,5-Dichlorosalicylic acid,99%;3,5-Dichlorosalicylic acid, 2-Carboxy-4,6-dichlorophenol;3,5-Dichlorosa licglic acid;3,5-Dichlorosalicylic acid,3,5-Dichloro-2-hydroxybenzoic acid;3,5-Dichlorosalicyli;2-Hydroxy-3,5-dichlorobenzoic acid;3,5-dichloro-2-hydroxybenzoate
CAS:320-72-9
MF:C7H4Cl2O3
MW:207.01
EINECS:206-281-8
Product Categories:Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
Mol File:320-72-9.mol
3,5-Dichlorosalicylic acid Chemical Properties
Melting point 220-222 °C (lit.)
Boiling point 297.29°C (rough estimate)
density 1.5281 (rough estimate)
refractive index 1.4845 (estimate)
storage temp. Inert atmosphere,Room Temperature
solubility Solubility in methanol (almost transparency).
pka1.99±0.14(Predicted)
form Solid
color White to Off-White
CAS DataBase Reference320-72-9(CAS DataBase Reference)
NIST Chemistry ReferenceBenzoic acid, 3,5-dichloro-2-hydroxy-(320-72-9)
EPA Substance Registry System3,5-Dichlorosalicyclic acid (320-72-9)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 36/37/38-22
Safety Statements 37/39-26-36
WGK Germany 3
RTECS VO2450000
TSCA Yes
HS Code 29182900
Hazardous Substances Data320-72-9(Hazardous Substances Data)
MSDS Information
ProviderLanguage
3,5-Dichlorosalicylic acid English
ACROS English
ALFA English
3,5-Dichlorosalicylic acid Usage And Synthesis
Chemical Propertieswhite crystalline powder
Uses3,5-Dichlorosalicylic acid is a bio-active drug and is a potential inhibitor of human 20α-hydroxysteroid dehydrogenase. It also finds its application as medicine and dyes intermediates.
General Description3,5-Dichlorosalicylic acid is a bio-active drug and its interaction with a model transport protein bovine serum albumin has been investigated. It is a potential inhibitor of human 20α-hydroxysteroid dehydrogenase.
Safety ProfilePoison by intraperitoneal route. When heated to decomposition it emits toxic fumes of Cl-.

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