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Home › Product Catalog › 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE

2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE

CAS 105650-23-5C13H12N4MW 224.26

2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE (CAS 105650-23-5) — formula C13H12N4, molecular weight 224.26; category organic chemicals.

Product Overview

CAS Number105650-23-5
Molecular FormulaC13H12N4
Molecular Weight224.26
Melting Point327 °C
LogPlog Kow = 2.23
ApplicationsUses: Mutagen present in cooked meat and fish, [Merck Index] Manufactured in small amounts for research purposes, [IARC], No known commerical uses.[DHHS, National Toxicology Program, Eleventh Report on Carcinogens: 2-Amino-1-Methyl-6-Phenylimidazo, 1-Methyl-6-phenyl-1H-imidazo[4, 5-b]pyridin-2-amine is a food-related mutagen, reported to be the most abundant heterocyclic amine found in cooked meat and fish., Methods of Manufacturing: 2-Amino-1-methyl-6-phenylimidazo[4, 5-b]pyridine has been prepared in 26% yield from 3-amino-2-phenylpropenal and creatinine which were heated with N, O-bis(trimethylsilyl)acetamide at 120 degrees C for 2 hr., General Manufacturing Information: ... heterocyclic amine formed during heating or cooking and, is, found in cooked meat and fish, Most abundant of the mutagenic heterocyclic amines found in well-cooked meat and fish, PhIP is produced in small quantities for research purposes. It is formed naturally during the cooking of muscle-derived foods (meat and fish) as by-products of the Maillard (or browning) reaction. It is postulated that the amino-imidazo part of, heterocyclic amines, (HCAs) is formed from creatine, while the remaining parts of the compound are likely formed from Strecker degradation products, such as pyridines or pyrazines, which are formed in the Maillard reaction between hexose sugars and amino acids. Formation of HCAs in food reportedly is affected by temperature, processing time, acidity, precursor concentrations, and types of amino acid present. In general, higher temperatures and longer cooking times increase the amount of HCAs produced. HCA formation also increases with cooking methods that use direct or efficient transfer of heat from the source to the food, frying or grilling of muscle meats produces more HCAs than do indirect-heat methods such as stewing, steaming, or poaching.[DHHS
CategoryOrganic Chemicals

Applications

Documented applications: Uses: Mutagen present in cooked meat and fish, [Merck Index] Manufactured in small amounts for research purposes, [IARC], No known commerical uses.[DHHS, National Toxicology Program, Eleventh Report on Carcinogens: 2-Amino-1-Methyl-6-Phenylimidazo, 1-Methyl-6-phenyl-1H-imidazo[4, 5-b]pyridin-2-amine is a food-related mutagen, reported to be the most abundant heterocyclic amine found in cooked meat and fish., Methods of Manufacturing: 2-Amino-1-methyl-6-phenylimidazo[4, 5-b]pyridine has been prepared in 26% yield from 3-amino-2-phenylpropenal and creatinine which were heated with N, O-bis(trimethylsilyl)acetamide at 120 degrees C for 2 hr., General Manufacturing Information: ... heterocyclic amine formed during heating or cooking and, is, found in cooked meat and fish, Most abundant of the mutagenic heterocyclic amines found in well-cooked meat and fish, PhIP is produced in small quantities for research purposes. It is formed naturally during the cooking of muscle-derived foods (meat and fish) as by-products of the Maillard (or browning) reaction. It is postulated that the amino-imidazo part of, heterocyclic amines, (HCAs) is formed from creatine, while the remaining parts of the compound are likely formed from Strecker degradation products, such as pyridines or pyrazines, which are formed in the Maillard reaction between hexose sugars and amino acids. Formation of HCAs in food reportedly is affected by temperature, processing time, acidity, precursor concentrations, and types of amino acid present. In general, higher temperatures and longer cooking times increase the amount of HCAs produced. HCA formation also increases with cooking methods that use direct or efficient transfer of heat from the source to the food, frying or grilling of muscle meats produces more HCAs than do indirect-heat methods such as stewing, steaming, or poaching.[DHHS.

Technical Profile

What this product is

2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE is a carbon-based organic compound with CAS registry number 105650-23-5 and molecular formula C13H12N4 (molecular weight 224.26), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 105650-23-5

Its molecular formula C13H12N4 comprises 13 C, 12 H, 4 N atoms.

Also known as: 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE · 2-氨基-1-甲基-6-苯基咪唑并[4,5-B]吡啶

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE?

The CAS registry number of 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE is 105650-23-5.

What is the molecular formula and molecular weight of 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE?

Molecular formula C13H12N4, molecular weight 224.26.

What other names is 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE known by?

It is also registered under: 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE, 2-氨基-1-甲基-6-苯基咪唑并[4,5-B]吡啶.

What are the documented applications of 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE?

Recorded applications: Uses: Mutagen present in cooked meat and fish, [Merck Index] Manufactured in small amounts for research purposes, [IARC], No known commerical uses.[DHHS, National Toxicology Program, Eleventh Report on Carcinogens: 2-Amino-1-Methyl-6-Phenylimidazo, 1-Methyl-6-phenyl-1H-imidazo[4, 5-b]pyridin-2-amine is a food-related mutagen, reported to be the most abundant heterocyclic amine found in cooked meat and fish., Methods of Manufacturing: 2-Amino-1-methyl-6-phenylimidazo[4, 5-b]pyridine has been prepared in 26% yield from 3-amino-2-phenylpropenal and creatinine which were heated with N, O-bis(trimethylsilyl)acetamide at 120 degrees C for 2 hr., General Manufacturing Information: ... heterocyclic amine formed during heating or cooking and, is, found in cooked meat and fish, Most abundant of the mutagenic heterocyclic amines found in well-cooked meat and fish, PhIP is produced in small quantities for research purposes. It is formed naturally during the cooking of muscle-derived foods (meat and fish) as by-products of the Maillard (or browning) reaction. It is postulated that the amino-imidazo part of, heterocyclic amines, (HCAs) is formed from creatine, while the remaining parts of the compound are likely formed from Strecker degradation products, such as pyridines or pyrazines, which are formed in the Maillard reaction between hexose sugars and amino acids. Formation of HCAs in food reportedly is affected by temperature, processing time, acidity, precursor concentrations, and types of amino acid present. In general, higher temperatures and longer cooking times increase the amount of HCAs produced. HCA formation also increases with cooking methods that use direct or efficient transfer of heat from the source to the food, frying or grilling of muscle meats produces more HCAs than do indirect-heat methods such as stewing, steaming, or poaching.[DHHS.

Which category does 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE belong to?

Category: Organic Chemicals.

PubChem Public Data

Independent reference data for 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE (CAS 105650-23-5), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number105650-23-5
PubChem CID1530
Molecular formulaC13H12N4
IUPAC name1-methyl-6-phenylimidazo[4,5-b]pyridin-2-amine
UNII (FDA)909C6UN66T

Computed descriptors

Molecular Weight224.26
XLogP32.2
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass224.106196400
Monoisotopic Mass224.106196400
Topological Polar Surface Area56.7
Heavy Atom Count17

Physicochemical values on record

Melting Point327 °C
Melting PointMP: 327-328 °C
Melting Point327 - 328 °C
Vapor Pressure0.00000001 [mmHg]
LogPlog Kow = 2.23
LogP2.23

Documented uses on record

    Mutagen present in cooked meat and fish; [Merck Index] Manufactured in small amounts for research purposes; [IARC]No known commerical uses.[DHHS/National Toxicology Program; Eleventh Report on Carcinogens: 2-Amino-1-Methyl-6-Phenylimidazo

    Synonyms and trade names

    PhIP; 105650-23-5; 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine; 1-methyl-6-phenyl-1H-imidazo[4,5-b]pyridin-2-amine; 2-Amino-1-methyl-6-phenylimidazo(4,5-b)pyridine; 1-Methyl-6-phenyl-1H-imidazo(4,5-b)pyridin-2-amine; 909C6UN66T; 1H-Imidazo(4,5-B)pyridin-2-amine, 1-methyl-6-phenyl-; CHEBI:76290; 2-amino-1-methyl-6-phenyl-1h-imidazo(4,5-b)pyridine; 2-amino-1-methyl-6-phenyl-1h-imidazo[4,5-b]pyridine; 2-AMP-IP cpd; RefChem:25903; 631-286-0; 1-methyl-6-phenylimidazo[4,5-b]pyridin-2-amine; MFCD00210745

    GHS hazard classification

    Reported hazard statementsH301 (97.6%), H315 (97.6%), H319 (97.6%), H335 (97.6%), H351 (97.6%)

    H301 (97.6%): Toxic if swallowed [Danger Acute toxicity, oral]

    H315 (97.6%): Causes skin irritation [Warning Skin corrosion/irritation]

    What the public record says

    2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE · CAS 105650-23-5 · C13H12N4. UNII 909C6UN66T. Melting Point: 327 °C; Melting Point: MP: 327-328 °C; Melting Point: 327 - 328 °C.

    Physical description and handling notes

    Source: PubChem / Wikidata; the batch COA governs where values differ.

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