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4-chloropyridine

CAS No.
626-61-9
Chemical Name:
4-chloropyridine
Synonyms
Pyridine, 4-chloro-;gamma-Chloropyridine;Trazodone Impurity 31;4-chloropyridine ISO 9001:2015 REACH
CBNumber:
CB3937772
Molecular Formula:
C5H4ClN
Molecular Weight:
113.54
MDL Number:
MFCD00044570
MOL File:
626-61-9.mol
MSDS File:
SDS
Last updated:2025-04-18 09:52:12
Product description Number Pack Size Price
4-Chloropyridine 95%+ 133694 500mg $365
4-CHLOROPYRIDINE 95.00% HCH0101467 5MG $505.78
4-Chloropyridine 95%+ 133694 1g $645
4-Chloropyridine 626619 250mg $680
4-Chloropyridine 626619 1g $1685
More product size

4-chloropyridine Properties

Melting point -43.5°C
Boiling point 147℃
Density 1.200
refractive index 1.5304 (estimate)
Flash point 53℃
pka 3.18±0.10(Predicted)
EWG's Food Scores 1

SAFETY

Risk and Safety Statements

Hazardous Substances Data 626-61-9(Hazardous Substances Data)

4-chloropyridine price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Matrix Scientific 133694 4-Chloropyridine 95%+ 626-61-9 500mg $365 2021-12-16 Buy
American Custom Chemicals Corporation HCH0101467 4-CHLOROPYRIDINE 95.00% 626-61-9 5MG $505.78 2021-12-16 Buy
Matrix Scientific 133694 4-Chloropyridine 95%+ 626-61-9 1g $645 2021-12-16 Buy
Alichem 626619 4-Chloropyridine 626-61-9 250mg $680 2021-12-16 Buy
Alichem 626619 4-Chloropyridine 626-61-9 1g $1685 2021-12-16 Buy
Product number Packaging Price Buy
133694 500mg $365 Buy
HCH0101467 5MG $505.78 Buy
133694 1g $645 Buy
626619 250mg $680 Buy
626619 1g $1685 Buy

4-chloropyridine Chemical Properties,Uses,Production

Uses

4-Chloropyridine is an inhibitor of nicotinamide N-methyltransferase (NNMT). It can act as a substrate for NNMT and, during its catalytic reaction, enhances the electrophilicity of the C4 position by methylating the nitrogen atom of the pyridine ring. This promotes an aromatic nucleophilic substitution reaction with the non-catalytic cysteine (C159) in NNMT, ultimately leading to the suicide inhibition of NNMT's activity. 4-Chloropyridine holds potential for the development of NNMT activity-based probes [1].

Purification Methods

Pour 4-chloropyridine into distilled water, and excess of 6M NaOH is added to give pH 12. The organic phase is separated and extracted with four volumes of diethyl ether. The combined extracts are filtered through paper to remove water, and the solvent is evaporated. The dark brown residual liquid is kept under high vacuum [Vaidya & Mathias J Am Chem Soc 108 5514 1986]. It can be distilled, but readily darkens and is best kept as the hydrochloride [7379-35-3] M 150.1, m 163-165o(dec). [Beilstein 20/5 V 410.]

References

[1] Sen S, et al. Development of a Suicide Inhibition-Based Protein Labeling Strategy for Nicotinamide N-Methyltransferase. ACS Chem Biol. 2019 Apr 19;14(4):613-618. DOI:10.1021/acschembio.9b00211

110-86-1
626-61-9
Synthesis of 4-chloropyridine from Pyridine
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View Lastest Price from 4-chloropyridine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
4-chloropyridine pictures 2025-11-18 4-chloropyridine
626-61-9
US $1.10 / g 1g 99.00% 100 Tons min Dideu Industries Group Limited

4-chloropyridine Spectrum

gamma-Chloropyridine Pyridine, 4-chloro- Trazodone Impurity 31 4-chloropyridine ISO 9001:2015 REACH 626-61-9