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Details

Stereochemistry ACHIRAL
Molecular Formula C7H7NO2.ClH
Molecular Weight 173.597
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-Pyridylacetic acid hydrochloride

SMILES

Cl.OC(=O)CC1=CC=CC=N1

InChI

InChIKey=MQVISALTZUNQSK-UHFFFAOYSA-N
InChI=1S/C7H7NO2.ClH/c9-7(10)5-6-3-1-2-4-8-6;/h1-4H,5H2,(H,9,10);1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C7H7NO2
Molecular Weight 137.136
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Lack of α-xylosidase activity in Arabidopsis alters xyloglucan composition and results in growth defects.
2010-11
Second-sphere tethering of rare-earth ions to cucurbit[6]uril by iminodiacetic acid involving carboxylic group encapsulation.
2010-10-04
trans-Diaqua-bis-[2-(2-pyrid-yl)acetato-κN,O]nickel(II).
2010-08-11
Comparative bioavailability of betahistine tablet formulations administered in healthy subjects.
2010
Automated potentiometric titrations in KCl/water-saturated octanol: method for quantifying factors influencing ion-pair partitioning.
2009-04-01
One-dimensional uranium-organic framework in catena-poly[[di-mu2-hydroxido-bis[dioxouranium(VI)]]-di-mu2-2-pyridylacetato-kappa(3)O,N:O';kappa(3)O:O',N].
2008-01
Separations of hydrophobic synthetic peptides in counter-current chromatography.
2007-06-01
Effects of hydrogen bonding on the ring stretching modes of pyridine.
2006-12-21
Pyridine-carboxylate complexes of platinum. Effect of N,O-chelate formation on model bifunctional DNA-DNA and DNA-protein interactions.
2005-07-25
Phosphoralaninate pronucleotides of pyrimidine methylenecyclopropane analogues of nucleosides: synthesis and antiviral activity.
2005
Synthesis and intramolecular reactions of Tyr-Gly and Tyr-Gly-Gly related 6-O-glucopyranose esters.
2004-01-02
LC-MS-MS analysis of 2-pyridylacetic acid, a major metabolite of betahistine: application to a pharmacokinetic study in healthy volunteers.
2003-12
Determination of carbocysteine in human plasma by liquid chromatography/tandem mass spectrometry employing precolumn derivatization.
2003
Effects of betahistine and of its metabolites on vestibular sensory organs.
2001-06
Patents
Substance Class Chemical
Created
by admin
on Tue Apr 01 20:13:47 GMT 2025
Edited
by admin
on Tue Apr 01 20:13:47 GMT 2025
Record UNII
7YM2824V24
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-83227
Preferred Name English
2-Pyridylacetic acid hydrochloride
Systematic Name English
2-Pyridineacetic acid, hydrochloride (1:1)
Systematic Name English
2-Carboxymethylpyridinium chloride
Systematic Name English
2-Pyridineacetic acid, hydrochloride
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID70884874
Created by admin on Tue Apr 01 20:13:47 GMT 2025 , Edited by admin on Tue Apr 01 20:13:47 GMT 2025
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PUBCHEM
85317
Created by admin on Tue Apr 01 20:13:47 GMT 2025 , Edited by admin on Tue Apr 01 20:13:47 GMT 2025
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FDA UNII
7YM2824V24
Created by admin on Tue Apr 01 20:13:47 GMT 2025 , Edited by admin on Tue Apr 01 20:13:47 GMT 2025
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ECHA (EC/EINECS)
240-316-8
Created by admin on Tue Apr 01 20:13:47 GMT 2025 , Edited by admin on Tue Apr 01 20:13:47 GMT 2025
PRIMARY
CAS
16179-97-8
Created by admin on Tue Apr 01 20:13:47 GMT 2025 , Edited by admin on Tue Apr 01 20:13:47 GMT 2025
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NSC
83227
Created by admin on Tue Apr 01 20:13:47 GMT 2025 , Edited by admin on Tue Apr 01 20:13:47 GMT 2025
PRIMARY