Quinaldic acid

Quinaldic acid Basic information
Product Name:Quinaldic acid
Synonyms:RARECHEM AL BO 1348;QUINOLINE-2-CARBOXYLIC ACID;QUINALDINIC ACID;QUINALDIC ACID;Quinoline-2-Carboxylic Acid (Quinaldic Acid) 99+%;Quinaldic acid, 99% 10GR;Quinaldic acid 98%;2-Quinolinecarboxylate
CAS:93-10-7
MF:C10H7NO2
MW:173.17
EINECS:202-218-3
Product Categories:Quinoline&Isoquinoline;Quinoline Derivertives;Acids and Derivatives;Heterocycles;Quinolinecarboxylic Acids, etc.;Quinolines;Building Blocks;Chemical Synthesis;Heterocyclic Building Blocks;Quinaldines
Mol File:93-10-7.mol
Quinaldic acid Structure
Quinaldic acid Chemical Properties
Melting point 156-158 °C (lit.)
Boiling point 247-250
density 1.2427 (rough estimate)
refractive index 1.5200 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility 14g/l
form Needle-Like Crystalline Powder
pka1.20±0.30(Predicted)
color Light brown
PH3.0-3.5 (10g/l, H2O, 20℃)
Water Solubility soluble
Merck 14,8046
BRN 126322
CAS DataBase Reference93-10-7(CAS DataBase Reference)
NIST Chemistry Reference2-Quinolinecarboxylic acid(93-10-7)
EPA Substance Registry System2-Quinolinecarboxylic acid (93-10-7)
Safety Information
Hazard Codes Xi,T
Risk Statements 36/37/38-23/24/25
Safety Statements 26-36-37/39-45-36/37/39
WGK Germany 3
RTECS UZ9100000
TSCA Yes
HazardClass IRRITANT
HS Code 29334990
MSDS Information
ProviderLanguage
2-Quinolinecarboxylic acid English
ACROS English
SigmaAldrich English
ALFA English
Quinaldic acid Usage And Synthesis
Chemical Propertieslight brown needle-like crystalline powder
UsesFor the determination of copper, zinc and uranium with which it forms insoluble salts.
Uses2-?Quinolinecarboxylic acid can be found in the studying of ligands for the purpose of copper-catalyzed Ullmann reactions with aryl ethers and aryl iodides.
DefinitionChEBI: A quinolinemonocarboxylic acid having the carboxy group at the 2-position.
Synthesis Reference(s)Journal of the American Chemical Society, 68, p. 1840, 1946 DOI: 10.1021/ja01213a045
General DescriptionQuinaldic acid is also referred as quinoline-2-carboxylic acid. Microwave-assisted preparation of substituted anilides of quinaldic acid has been reported. It inhibits the oxidation of pyruvate, α-ketoglutarate, glutamate and citrate in rat liver mitochondria. Quinaldic acid is a metabolite of tryptophan degradation and inhibits the gluconeogenesis in perfused livers.
Purification MethodsCrystallise quinaldic acid from *C6H6 or AcOH. It is used for the estimation of many metals. The methyl ester has m 86-87o (from hexane) and pK25 1.76. [Chauduri et al. Frez Z Anal Chem 281 361 1976, Beilstein 22 H 71, 22 II 55, 22 III/IV 1149, 22/3 V 183.]
5,7-DICHLOROKYNURENIC ACID SODIUM SALT Nalidixic acid Quinoline Ethyl 2-(Chlorosulfonyl)acetate Quinclorac 2,3-Quinoline dicarboxylic acid QUINALDIC ACID SODIUM SALT 98+%,QUINALDIC ACID SODIUM SALT Folic acid Ethoxyquin Glycine 2,3,4-Trihydroxybenzoic acid 8-Hydroxyquinaldine Quinaldine Quinaldic acid CARBOXYLIC ACID 2,4-Dichlorobenzoic acid Quetiapine fumarate Citric acid

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