6-Aminopyridine-3-c...

6-Aminopyridine-3-carboxamide
6-Aminopyridine-3-carboxamide
6-Aminopyridine-3-carboxamide

6-Aminopyridine-3-carboxamide

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1 Kilogram

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6-Aminopyridine-3-carboxamide 329-89-5 C6H7N3O

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  • Appearance:powder
  • Application:329-89-5
  • PackAge:as requested
  • ProductionCapacity:300|Kilogram|Month
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6-Aminopyridine-3-carboxamide Basic information
Product Name: 6-Aminopyridine-3-carboxamide
Synonyms: 2-AMINOPYRIDINE-5-CARBOXAMIDE;6-AMINOPYRIDINE-3-CARBOXAMIDE;6-AMINONICOTINAMIDE;6-AMINO-3-PYRIDINECARBOXAMIDE;2-Amino-5-carbamoylpyridine;3-Pyridinecarboxamide, 6-amino-;6-amino-3-pyridinecarboxamid;6-amino-nicotinamid
CAS: 329-89-5
MF: C6H7N3O
MW: 137.14
EINECS: 206-349-7
Product Categories: AMIDE;Pyridine series;Amines;Pyridines;Heterocyclic Compounds;Building Blocks;C6;Chemical Synthesis;Heterocyclic Building Blocks
Mol File: 329-89-5.mol
6-Aminopyridine-3-carboxamide Structure
 
6-Aminopyridine-3-carboxamide Chemical Properties
Melting point  245-248 °C(lit.)
BRN  116042
CAS DataBase Reference 329-89-5(CAS DataBase Reference)
NIST Chemistry Reference Nicotinamide, 6-amino-(329-89-5)
 
Safety Information
Hazard Codes  T
Risk Statements  61
Safety Statements  53-45
RIDADR  1655
WGK Germany  3
RTECS  US4550000
Hazard Note  Toxic
PackingGroup  II
MSDS Information
Provider Language
SigmaAldrich English
ALFA English
 
6-Aminopyridine-3-carboxamide Usage And Synthesis
Usage antineoplastic, apoptosis inducer
General Description White crystalline solid.
Air & Water Reactions Insoluble in water.
Reactivity Profile An amine and amide. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).
Health Hazard ACUTE/CHRONIC HAZARDS: When heated to decomposition 6-Aminopyridine-3-carboxamide emits toxic fumes of NOx.
Fire Hazard Flash point data for 6-Aminopyridine-3-carboxamide are not available; however, 6-Aminopyridine-3-carboxamide is probably combustible.
 
6-Aminopyridine-3-carboxamide Preparation Products And Raw materials

 

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