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InChI=1S/C6H9N11/c7-1-11-2(8)14-5(13-1)17-6-15-3(9)12-4(10)16-6/h(H9,7,8,9,10,11,12,13,14,15,16,17)
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InChI=1/C6H9N11/c7-1-11-2(8)14-5(13-1)17-6-15-3(9)12-4(10)16-6/h(H9,7,8,9,10,11,12,13,14,15,16,17)
427:-(4,6-diamino-1,3,5-triazin-2-yl)-1,3,5-triazine-2,4,6-triamine) is a condensation product of
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Except where otherwise noted, data are given for materials in their
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B. Bann and S.A. Miller, "Melamines and derivatives of melamine",
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52:-(4,6-Diamino-1,3,5-triazin-2-yl)-1,3,5-triazine-2,4,6-triamine
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478:Upon heating, melam first loses ammonia to form
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459:, melam undergoes hydrolysis to form
299:C1(=NC(=NC(=N1)NC2=NC(=NC(=N2)N)N)N)N
268:Key: YZEZMSPGIPTEBA-UHFFFAOYSA-N
467:. It also reacts with concentrated
450:
443:in 1834 from the residue of heating
278:Key: YZEZMSPGIPTEBA-UHFFFAOYAX
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382:(at 25 °C , 100 kPa).
60:A1,3,5-Triazine-2,4,6-triamine
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501:, vol.58, p131-172 (1958).
372:slightly soluble in acids
342:235.21 g/mol
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439:Melam was discovered by
455:In the presence of 30%
445:ammonium thiocyanate
357:Solubility in water
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409:Infobox references
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451:Chemical property
417:Chemical compound
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221:CompTox Dashboard
107:Interactive image
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520:Secondary amines
498:Chemical Reviews
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315:Chemical formula
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380:standard state
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473:cyanuric acid
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350:white powder
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66:Identifiers
58:Other names
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482:, and then
469:nitric acid
347:Appearance
308:Properties
145:100.020.632
525:Polyamines
509:Categories
490:References
368:Solubility
362:insoluble
338:Molar mass
209:763B6VP74S
118:ChemSpider
94:3D model (
73:CAS Number
46:IUPAC name
515:Triazines
435:Synthesis
166:222-695-1
158:EC Number
83:3576-88-3
465:melamine
461:ammeline
429:melamine
457:ammonia
402:what is
400: (
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176:PubChem
441:Liebig
397:verify
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292:SMILES
40:Names
17:Melam
484:melon
480:melem
421:Melam
257:InChI
189:77125
127:69563
96:JSmol
463:and
200:UNII
226:EPA
179:CID
511::
486:.
475:.
447:.
431:.
425:N2
330:11
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423:(
392:N
328:N
326:9
324:H
322:6
320:C
228:)
224:(
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