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Quinaldic acid

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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
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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
pka
1.20±0.30(Predicted)
color 
Light brown
PH
3.0-3.5 (10g/l, H2O, 20℃)
Water Solubility 
soluble
Merck 
14,8046
BRN 
126322
CAS DataBase Reference
93-10-7(CAS DataBase Reference)
NIST Chemistry Reference
2-Quinolinecarboxylic acid(93-10-7)
EPA Substance Registry System
2-Quinolinecarboxylic acid (93-10-7)
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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

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Quinaldic acid Usage And Synthesis

Chemical Properties

light brown needle-like crystalline powder

Uses

2-?Quinolinecarboxylic acid can be found in the studying of ligands for the purpose of copper-catalyzed Ullmann reactions with aryl ethers and aryl iodides.

Uses

For the determination of copper, zinc and uranium with which it forms insoluble salts.

Definition

ChEBI: 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 Description

Quinaldic 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 Methods

Crystallise 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.]

Quinaldic acid Preparation Products And Raw materials

Raw materials

Preparation Products

Quinaldic acidSupplier

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