SDSDownload

2-Amino-4-methylpyridine / 100 G

Purity: 99 %
Synonym: Ascensil; Aminopicoline; 2-Amino-4-picoline; 4-Methyl-2-pyridinamine; 4-Methyl-2-aminopyridine; 4-METHYLPYRIDIN-2-AMINE
Molecular Formula: C6H8N2
Molecular Weight: 108.14
SKU: MND-44096
CAS Number: 695-34-1
MDL number: MFCD00006321
EC Number: 211-780-9
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 100 G  
37.38 EUR



Safety Information


Hazard Statements

H301 + H311 + H331
H412
H314

Precautionary Statements

P280
P303 + P361 + P353
P273
P305 + P351 + P338
P304 + P340 + P310
P260

Pictograms



Properties

Signal WordDanger
Flash Point (C)118 °C - closed cup
Flash Point (F)244.4 °F - closed cup
Boiling Point230 °C (lit.)
Melting Point96-99 °C (lit.)

 Product Description

2-AMINO-4-METHYLPYRIDINE is a chemical compound often used as a building block in the synthesis of pharmaceuticals, agrochemicals, and organic compounds due to its functional groups and reactivity.

 

Application:

2-AMINO-4-METHYLPYRIDINE is commonly employed in the pharmaceutical and agrochemical industries as a key intermediate in the production of various drugs and crop protection chemicals.

 

 

Articles:

- 2-Amino-4-methylpyridine as a potent inhibitor of inducible NO synthase activity in vitro and in vivo

Publication Date: November 1996

W. Stephen Faraci, Arthur A. Nagel, Kimberly A. Verdries, Lawrence A. Vincent, Hong Xu, Lois E. Nichols, Jeffrey M. Labasi, Eben D. Salter, E. Roy Pettipher

https://doi.org/10.1111/j.1476-5381.1996.tb16010.x

 

- Inhibition of Nitric Oxide Synthase Aggravates Cisplatin-Induced Nephrotoxicity: Effect of 2-Amino-4-Methylpyridine

Publication Date: APRIL 10 2003

Sherif Y. Saad; Tawfeeg A.O. Najjar; Mohammed H. Daba; Ammar C. Al-Rikabi

https://doi.org/10.1159/000069714

 

- Hydrogen Bonded Supramolecular Association in Organic Acid–Base Salts: Crystal Structures of Four Proton-Transfer Complexes Assembled from 2-Amino-4-methylpyridine with 2-Chloro, 4-Chloro, 3-Methyl and 4-Methylbenzoic Acid

Publication Date: 07 October 2014

Nuridayanti Che Khalib, Kaliyaperumal Thanigaimani, Suhana Arshad & Ibrahim Abdul Razak

https://doi.org/10.1007/s10870-014-0550-2