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2-Aminonicotinic acid

CAS No.
5345-47-1
Chemical Name:
2-Aminonicotinic acid
Synonyms
2-AMINOPYRIDINE-3-CARBOXYLIC ACID;NSC 3049;AKOS 92162;2- aMinoacid;H-NH(2)NICOT-OH;H-NH(2)PYRD(3)-OH;AKOS BBS-00003845;TIMTEC-BB SBB004188;RARECHEM AL BO 2388;2-AMINONICOTINIC ACID
CBNumber:
CB0120818
Molecular Formula:
C6H6N2O2
Molecular Weight:
138.12
MDL Number:
MFCD00006318
MOL File:
5345-47-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 14:58:52
Product description Number Pack Size Price
2-Aminopyridine-3-carboxylic acid 98% A68300 5g $64
2-Aminopyridine-3-carboxylic acid 98% A68300 25g $126
2-Aminonicotinic Acid >98.0%(T) A0994 5g $28
2-Aminonicotinic Acid >98.0%(T) A0994 25g $82
2-AMINONICOTINIC ACID 97% CX1070 5G $23
More product size

2-Aminonicotinic acid Properties

Melting point 295-297 °C (dec.)(lit.)
Boiling point 253.51°C (rough estimate)
Density 1.3471 (rough estimate)
refractive index 1.5100 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility DMSO
form Crystalline Powder
pka 2.94±0.10(Predicted)
color Off-white to light yellow
Water Solubility soluble
BRN 119031
InChI InChI=1S/C6H6N2O2/c7-5-4(6(9)10)2-1-3-8-5/h1-3H,(H2,7,8)(H,9,10)
InChIKey KPIVDNYJNOPGBE-UHFFFAOYSA-N
SMILES C1(N)=NC=CC=C1C(O)=O
CAS DataBase Reference 5345-47-1(CAS DataBase Reference)
EPA Substance Registry System 2-Aminonicotinic acid (5345-47-1)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
PPE Eyeshields, Gloves, type N95 (US)
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  22-24/25-37/39-26-36
WGK Germany  3
TSCA  TSCA listed
HazardClass  IRRITANT
HS Code  29333999
Storage Class 11 - Combustible Solids
NFPA 704
0
2 0

2-Aminonicotinic acid price More Price(51)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich A68300 2-Aminopyridine-3-carboxylic acid 98% 5345-47-1 5g $64 2026-04-30 Buy
Sigma-Aldrich A68300 2-Aminopyridine-3-carboxylic acid 98% 5345-47-1 25g $126 2026-04-30 Buy
TCI Chemical A0994 2-Aminonicotinic Acid >98.0%(T) 5345-47-1 5g $28 2026-04-30 Buy
TCI Chemical A0994 2-Aminonicotinic Acid >98.0%(T) 5345-47-1 25g $82 2026-04-30 Buy
AstaTech CX1070 2-AMINONICOTINIC ACID 97% 5345-47-1 5G $23 2026-04-30 Buy
Product number Packaging Price Buy
A68300 5g $64 Buy
A68300 25g $126 Buy
A0994 5g $28 Buy
A0994 25g $82 Buy
CX1070 5G $23 Buy

2-Aminonicotinic acid Chemical Properties,Uses,Production

Structure

2-aminonicotinic acid (or 2-aminopyridine-3-carboxylic acid, abbreviated ANA) can be a model compound for reactions containing carboxylic and amino groups attached to the pyridine ring. X-ray diffraction studies have shown that in the molecular crystal phase, ANA occurs as a zwitterion in which protonation occurs at the nitrogen atom of the pyridine ring. Infrared spectra of ANA molecular crystal have confirmed that intra- and intermolecular hydrogen bonds are present in its structure. Karabacak et al. investigated the tautomerism of ANA using electronic structure calculations (B3LYP/6-311++G(d,p)) and identified four amino tautomers. Furthermore, Nayak and Dogra optimized the structures of two amino and two imino structures at the B3LYP/6-31G** level. On the basis of both experimental data (absorption and fluorescence spectra) and electronic structure calculations, these authors concluded that ANA is present in solutions as the amino form in both the S0 and S1 states, whereas the imino forms are absent. ANA exists as a molecular species in non-polar and polar aprotic solvents and as a zwitterion in polar protic solvents[1].

Chemical Properties

Off-white to light yellow crystalline powder

Uses

2-Aminopyridine-3-carboxylic acid can be used as:

  • A ligand to prepare copper(II)-organic coordination compounds.
  • A reactant to prepare pyrido[2′,1′:2,3]imidazo[4,5-c]isoquinolines by reacting with trimethylsilyl cyanide and phthalaldehyde.
  • A reactant to synthesize organo-soluble and thermally stable poly(thiourea-amide-imide) polymers.

Uses

A component of hair dyes.

Definition

ChEBI: An aminonicotinic acid in which the amino group is situated at position 2 of the pyridine ring.

Application

2-Aminonicotinic acid may be employed as a chemiluminescent derivatisation reagent for the determination of methylglyoxal. Following a four-hour reaction with methylglyoxal in an acidic solution at 37°C, this reagent produces chemiluminescence in a solution of N,N'-dimethylformamide containing sodium tert-butoxide. The detection limit for methylglyoxal in this reaction system is 233 fmol[2].

Synthesis

2-(AMINOCARBONYL)NICOTINIC ACID

5860-70-8

2-Aminonicotinic acid

5345-47-1

Step 4. 30 mL of 5 mol-L1 sodium hydroxide solution was added to a 100 mL flask and cooled to 5 °C. After cooling to 5 °C, 0.02 mol of bromine was added slowly and the reaction was stirred for 0.5 hours. Subsequently, 0.02 mol 2-aminopyridine-3-carboxylic acid was added and the temperature was raised to 85 °C and kept for 2 hours for the reaction. Step 5: After completion of the reaction, the reaction mixture was concentrated under reduced pressure to remove some of the solvent. After cooling, the pH was adjusted to 7 with dilute hydrochloric acid and the precipitate was collected by filtration. The resulting solid was dried and evaporated to give final crystals of 2-aminopyridine-3-carboxylic acid as a white solid.

References

[1] M. Pagacz-Kostrzewa . “Phototransformations of 2-aminonicotinic acid resolved with matrix isolation infrared spectroscopy and ab initio calculations.” Journal of Photochemistry and Photobiology A-chemistry 410 (2021): Article 113187.
[2] R. SONNENBURG. ChemInform Abstract: Synthesis of Phosphorus-Containing Heterocycles from 2-Aminonicotinic Acid.[J]. ChemInform, 1995, 26 39. DOI:10.1002/chin.199539193.

2942-59-8
5345-47-1
Synthesis of 2-Aminonicotinic acid from 2-Chloronicotinic acid
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View Lastest Price from 2-Aminonicotinic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-Aminonicotinic acid pictures 2026-05-18 2-Aminonicotinic acid
5345-47-1
US $0.00-0.00 / Kg/Drum 1KG 98%min 10 tons WUHAN FORTUNA CHEMICAL CO., LTD
2-Aminonicotinic acid pictures 2026-05-18 2-Aminonicotinic acid
5345-47-1
US $100.00-75.00 / kg 1kg 99% 5000 HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
2-Aminonicotinic acid pictures 2026-03-20 2-Aminonicotinic acid
5345-47-1
US $1.00 / KG 1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
2-AMino-3-carboxypyridine Nicotinic acid, 2-aMino- (6CI,7CI,8CI) 2-Aminopyridine-3-carboxylic acid, 2-Amino-3-carboxypyridine NSC 3049 2- aMinoacid 2-AMINO-3-PYRIDINECARBOXYLIC ACID 2-AMINONICOTINIC ACID H-NH(2)NICOT-OH H-NH(2)PYRD(3)-OH 2-Aminonicotinic acid;2-Aminopyridine-3-carboxylic acid 2-Aminopyridin-3-carboxylic acid for synthesis 2-AMINO-3-PYRIDINECARBOYXLIC ACID 2-Aminonicotinic acid, 98+% 3-Pyridinecarboxylic acid, 2-amino- 2-Aminonicotinic acid 98% 3-Pyridinecarboxylicacid,2-amino-(9CI) 2-Aminopyridine-3-carboxylic acid 98% 2-Amino-3-pyridinecarboxylic 2-animonicotinic acid TIMTEC-BB SBB004188 RARECHEM AL BO 2388 2-aMinopyridine-3-carbo×ylic acid 2-amino-3-pyridinecarboxylicaci AKOS BBS-00003845 AKOS 92162 2-Aminonicotinic Acid > 2-aminotinicotinic acid 2-Aminonicotinic acid USP/EP/BP 2-AMINOPYRIDINE-3-CARBOXYLIC ACID Diclofenac Potassium BP2010EP6 Abemaciclib Impurity 19 2-Aminopyridine-3-carboxylic acid, 95% 5345-47-1 5345-47-2 5345-47-3 5354-47-1 C6H7N2O2 Building Blocks Acid Heterocyclic Building Blocks Pyridines C6 Building Blocks Chemical Synthesis Heterocyclic Building Blocks AMINOACID Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts Carboxylic Acids Pyridine Pyridines derivates Amino Acids and Derivatives Heterocycles Amines blocks Carboxes Pyridines Carboxylic Acids Aromatics