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M2659

Sigma-Aldrich

Melamine

99%

Synonym(s):

2,4,6-Triamino-1,3,5-triazine, sym-Triaminotriazine

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About This Item

Empirical Formula (Hill Notation):
C3H6N6
CAS Number:
Molecular Weight:
126.12
Beilstein:
124341
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

powder

mp

>300 °C (lit.)

solubility

water: soluble 25 mg/mL, clear to slightly hazy, colorless

SMILES string

Nc1nc(N)nc(N)n1

InChI

1S/C3H6N6/c4-1-7-2(5)9-3(6)8-1/h(H6,4,5,6,7,8,9)

InChI key

JDSHMPZPIAZGSV-UHFFFAOYSA-N

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Application

Melamine can be used as a:
  • Reactant in the preparation of melamine trisulfonic acid (MTSA) which is used as a catalyst in various reactions.
  • Nitrogen source for the large scale synthesis of nitrogen-doped graphene (NG).
  • Heterogeneous catalyst in combination with lewis acid ZnI2 for conversion of carbon dioxide to cyclic carbonates.

Pictograms

Health hazard

Signal Word

Warning

Hazard Statements

Hazard Classifications

Carc. 2 - Repr. 2 - STOT RE 2

Target Organs

Urinary tract

WGK

WGK 1

Flash Point(F)

572.0 °F

Flash Point(C)

300 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Melamine trisulfonic acid (MTSA): a new efficient catalyst for the chemoselective methoxymethylation of alcohols.
Shirini F, et al.
Synthetic Communications, 40(6), 910-914 (2010)
Effect of melamine and its salts on combustion and thermal decomposition of polyamide 6.
Levchik SV, et al.
Fire and Materials, 21(2), 75-83 (1997)
The crystal structure of melamine.
Hughes EW.
Journal of the American Chemical Society, 63(6), 1737-1752 (1941)
Infrared and Raman spectra of melaminium chloride hemihydrate.
Marchewka M K.
Materials Science and Engineering, B, 95(3), 214-221 (2002)
Melamine-ZnI2 as heterogeneous catalysts for efficient chemical fixation of carbon dioxide to cyclic carbonates.
Liu M, et al.
Royal Society of Chemistry Advances, 5(2), 960-966 (2015)

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