105650-23-5

  • Product Name:2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE
  • Molecular Formula:C13H12N4
  • Molecular Weight:224.265
  • Appearance:Off-white solid
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Product Details

pd_meltingpoint:300 °C

Appearance:Off-white solid

Purity:99%

Top Quality 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE 105650-23-5 Hot Sell In Stock

  • Molecular Formula:C13H12N4
  • Molecular Weight:224.265
  • Appearance/Colour:Off-white solid 
  • Vapor Pressure:5.74E-09mmHg at 25°C 
  • Melting Point:300 °C 
  • Refractive Index:1.699 
  • Boiling Point:468.94 °C at 760 mmHg 
  • PKA:7.72±0.30(Predicted) 
  • Flash Point:237.407 °C 
  • PSA:56.73000 
  • Density:1.3 g/cm3 
  • LogP:2.79870 

2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE(Cas 105650-23-5) Usage

Safety Profile

Confirmed carcinogen with experimental carcinogenic data. Mutation data reported. When heated to decomposition it emits toxic vapors of NOx,.

Carcinogenicity

PhIP is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals and supporting genotoxicity data.

Definition

ChEBI: An imidazopyridine that is 1H--imidazo[4,5-b]pyridine which is substituted at positions 1, 2, and 6 by methyl, amino, and phenyl groups, respectively. It is the most abundant of the mutagenic heterocyclic amines found in coo ed meat and fish.

InChI:InChI=1/C13H12N4/c1-17-11-7-10(9-5-3-2-4-6-9)8-15-12(11)16-13(17)14/h2-8H,1H3,(H2,14,15,16)

105650-23-5 Relevant articles

Synthesis of a new isomer of creatinine and its use in the preparation of the food mutagen 2-amino-1-methyl-6-phenyl-1H-imidazo[4,5-b]pyridine (PHIP)

Bergman, Jan

, p. 5631 - 5632 (2009)

Base-induced cyclization of N′-cyanometh...

Indole: A Promising Scavenging Agent for Methylglyoxal and Related Carbonyls in Tryptophan Containing Maillard Model Systems

Ghassem Zadeh, Raheleh,Yaylayan, Varoujan

, p. 6359 - 6365 (2019)

In situ generation of efficient carbonyl...

A test of the mutagenicity of cooked meats in vivo

Heddle, John A.,Knize, Mark G.,Dawod, David,Zhang, Xue-Bin

, p. 103 - 107 (2001)

There is a correlation between intestina...

Cross-coupling reaction of 2-halo1-methyl-1H-imidazo[4,5-b]pyridine offers a new synthetic route to mutagenic heterocyclic amine-PHIP and DMIP

Sajith, Ayyiliath M.,Muralidharan, Arayambath,Karuvalam, Ranjith P.,Haridas, Karickal R.

supporting information, p. 361 - 364 (2013/07/26)

A modified synthetic approach to the syn...

Synthesis and mutagenic potency of structural isomers of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine

Chrisman,Knize,Tanga

experimental part, p. 1641 - 1649 (2009/08/09)

(Chemical Equation Presented) Synthesis ...

105650-23-5 Process route

1-methyl-6-phenyl-1H-imidazo[4,5-b]pyridine
125572-33-0

1-methyl-6-phenyl-1H-imidazo[4,5-b]pyridine

2-amino-1-methyl-6-phenyl-1H-imidazo[4,5-b]pyridine
105650-23-5

2-amino-1-methyl-6-phenyl-1H-imidazo[4,5-b]pyridine

Conditions
Conditions Yield
With sodium amide; In xylene; at 130 ℃; for 1.5h;
90.2%
With sodium amide;
80%
With 15-crown-5; sodium amide; In xylene; at 130 ℃; for 1.5h;
20 % Turnov.
2-amino-1-methylbenzothieno[3,2-e]imidazo[4,5-b]pyridine
878996-00-0

2-amino-1-methylbenzothieno[3,2-e]imidazo[4,5-b]pyridine

2-amino-1-methyl-6-phenyl-1H-imidazo[4,5-b]pyridine
105650-23-5

2-amino-1-methyl-6-phenyl-1H-imidazo[4,5-b]pyridine

Conditions
Conditions Yield
With sodium hydroxide; nickel; In 1,4-dioxane; ethanol; Heating;
35%

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