160660
Quinaldic acid
98%
Synonym(s):
2-Quinolinecarboxylic acid
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| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 2.5 g | Please contact Customer Service for Availability | £29.20 | |
| 10 g | Please contact Customer Service for Availability | £34.70 |
About This Item
Empirical Formula (Hill Notation):
C10H7NO2
CAS Number:
Molecular Weight:
173.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-218-3
Beilstein/REAXYS Number:
126322
MDL number:
Assay:
98%
Form:
solid
Quality Level
assay
98%
form
solid
mp
156-158 °C (lit.)
functional group
carboxylic acid
SMILES string
OC(=O)c1ccc2ccccc2n1
InChI
1S/C10H7NO2/c12-10(13)9-6-5-7-3-1-2-4-8(7)11-9/h1-6H,(H,12,13)
InChI key
LOAUVZALPPNFOQ-UHFFFAOYSA-N
General description
Quinaldic acid is also referred as quinoline-2-carboxylic acid. Microwave-assisted preparation of substituted anilides of quinaldic acid has been reported.[1] It inhibits the oxidation of pyruvate, α-ketoglutarate, glutamate and citrate in rat liver mitochondria.[2] Quinaldic acid is a metabolite of tryptophan degradation and inhibits the gluconeogenesis in perfused livers.[2]
1 of 1
This Item | |||
|---|---|---|---|
| assay 98% | assay ≥95.0% (GC) | assay 97% | assay ≥99.5% |
| Quality Level 200 | Quality Level - | Quality Level 200 | Quality Level 200 |
| form solid | form liquid | form - | form - |
| mp 156-158 °C (lit.) | mp −9-−3 °C (lit.) | mp - | mp −24-−23 °C (lit.) |
| functional group carboxylic acid | functional group - | functional group bromo, carboxylic acid | functional group - |
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Pavel Bobal et al.
Molecules (Basel, Switzerland), 17(2), 1292-1306 (2012-02-02)
In this study a one step method for the preparation of substituted anilides of quinoline-2-carboxylic acid was developed. This efficient innovative approach is based on the direct reaction of an acid or ester with substituted anilines using microwave irradiation. The
Stereocontrolled synthesis of the quinaldic acid macrocyclic system of thiostrepton.
K C Nicolaou et al.
Angewandte Chemie (International ed. in English), 41(11), 1937-1940 (2002-06-03)
K Jhamandas et al.
Brain research, 529(1-2), 185-191 (1990-10-08)
Certain products of tryptophan metabolism interact with excitatory amino acid receptors to produce or protect against excitotoxicity. In this study, the action of several tryptophan metabolites, yielded by the kynurenine pathway, on cortical cholinergic toxicity was evaluated following focal injection
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 160660-2.5G | 04061833464533 |
| 160660-10G | 04061838346360 |