Customization: | Available |
---|---|
CAS No.: | 108-78-1 |
Formula: | C3h6n6 |
Suppliers with verified business licenses
Audited by an independent third-party inspection agency
Melamine
1,3,5-Triazine-2,4,6-triamine;Melamine;s-Triazine,4,6-diamino-1,2-dihydro-2-imino-;Cyanuramide;Cyanurotriamide;Cyanurotriamine;2,4,6-Triamino-s-triazine;1,3,5-Triazine-2,4,6(1H,3H,5H)-triimine;Triaminotriazine;Isomelamine;2,4,6-Triaminotriazine;Teoharn;Theoharn;Virset 656-4;2,4,6-Triamino-1,3,5-triazine;s-Triazinetriamine;Pluragard C 133;Pluragard;Triamino-s-triazine;DG 002 (amine);DG 002;ZS 27;ADK Stab ZS 27;Mark ZS 27;Yukamelamine;Spinflam ML 94M;2,4,6-Triamino-1,2,3-triazine;PC 1;NSC 2130;Flammex MEL;Mitsui 2020A;Melamine 2020A;Melafine;Mel F 40;Melamine HM;Micromel 325;T 518;H 882;PMN 500;M 2659;Relugan XD;SM 1013;D-ACE 557;GPH-LD;JLS Melamine;A 11295;Aflammit PMN 500;AF-PMN 500;MEL AR;504-18-7;65544-34-5;67757-43-1;68379-55-5;70371-19-6;94977-27-2;130392-03-9;169314-62-9;1228929-27-8;1399841-69-0;1399841-71-4;1399841-73-6
108-78-1
InChIKey=JDSHMPZPIAZGSV-UHFFFAOYSA-N
126.12000
126.12
203-615-4
N3GP2YSD88
1154
8152|2130
DTXSID6020802
Monoclinic prisms|Monoclinic colorless prisms or crystals|White, monoclinic crystals
Heterocyclic Ring
116.73000
-1.4
Melamine appears as colorless to white monoclinic crystals or prisms or white powder. Sublimes when gently heated. (NTP, 1992)
1.573 g/cm3 @ Temp: 14 °C
<250 °C
299.696ºC at 760 mmHg
135.052ºC
1.922
H2O: 3 g/L (20 ºC)
-20ºC
0.001mmHg at 25°C
4.34 (Air= 1)
LD50 orally in Rabbit: 3161 mg/kg LD50 dermal Rabbit > 1000 mg/kg
Henry's Law constant = 1.84X10-14 atm-cu m/mol at 25 °C (est)
pKa = 5.0
Heat of sublimation = -121 kJ/mol at 25 °C|Hydroxyl radical reaction rate constant = 6.6X10-13 cu cm/molec-sec at 25 °C (est)
Insoluble in water.
Amines, Phosphines, and Pyridines
MELAMINE is incompatible with strong oxidizing agents and strong acids (NTP, 1992). Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.
greater than 500 °F (NTP, 1992)|>500 °C
-1967 kJ/mol at 25 °C
Dust explosion possible if in powder or granular form, mixed with air.