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329-89-5

329-89-5 Structure

329-89-5 Structure
IdentificationMore
【Name】

6-Aminopyridine-3-carboxamide
【CAS】

329-89-5
【Synonyms】

2-AMINOPYRIDINE-5-CARBOXAMIDE
6-AMINO-3-PYRIDINECARBOXAMIDE
6-AMINONICOTINAMIDE
6-AMINOPYRIDINE-3-CARBOXAMIDE
2-Amino-5-carbamoylpyridine
3-Pyridinecarboxamide, 6-amino-
6-amino-3-pyridinecarboxamid
6-amino-nicotinamid
6-Aminonicotinic acid amide
6-aminonicotinicacidamide
6-Amino-nicotinsaeureamid
6-Aminonikotinsaeureamid
6-AN
6-ANA
Aminonicotinamide
FDA 0121
fda0121
NSC 21206
nsc21206
U-8774
【EINECS(EC#)】

206-349-7
【Molecular Formula】

C6H7N3O
【MDL Number】

MFCD00006327
【Molecular Weight】

137.14
【MOL File】

329-89-5.mol
Chemical PropertiesBack Directory
【mp 】

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 DataBack Directory
【Hazard Codes 】

T
【Risk Statements 】

R61:May cause harm to the unborn child.
【Safety Statements 】

S53:Avoid exposure - obtain special instruction before use .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
【RIDADR 】

1655
【WGK Germany 】

3
【RTECS 】

US4550000
【Hazard Note 】

Toxic
【PackingGroup 】

II
Hazard InformationBack Directory
【General Description】

White crystalline solid.
【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).
【Air & Water Reactions】

Insoluble in water.
【Health Hazard】

ACUTE/CHRONIC HAZARDS: When heated to decomposition this compound emits toxic fumes of NOx.
【Fire Hazard】

Flash point data for this chemical are not available; however, 6-AMINONICOTINAMIDE(329-89-5) is probably combustible.
Spectrum DetailBack Directory
【Spectrum Detail】

6-Aminopyridine-3-carboxamide(329-89-5)1HNMR
6-Aminopyridine-3-carboxamide(329-89-5)13CNMR
6-Aminopyridine-3-carboxamide(329-89-5)IR1
6-Aminopyridine-3-carboxamide(329-89-5)MS
6-Aminopyridine-3-carboxamide(329-89-5)IR2
Well-known Reagent Company Product InformationBack Directory
【Alfa Aesar】

6-Aminonicotinamide, 99%(329-89-5)
【Sigma Aldrich】

329-89-5(sigmaaldrich)
【TCI AMERICA】

6-Aminonicotinamide,>99.0%(T)(329-89-5)
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