Melamine - 10mM in DMSO , CAS No.108-78-1

CAS: 108-78-1 Cat. No.: M420556 Formula: C₃H₆N₆ Molecular Weight: 126.12 Beilstein Registry Number: 124341 EC Number: 203-615-4

GRADE & PURITY 10mM in DMSO

Synonyms

MELAMINE (IARC)|Melamine; 1,3,5-Triazine-2,4,6-triamine|2,6-Triamino-1,3,5-triazine|s-Triazine,4,6-triamino-|sym-Triaminotriazine|Triaminotriazine|MELAMINE (USP-RS)|Spinflam ML 94M|s-triaminotriazine|DG 002 (amine)|melamin|MELAMINE [USP-RS]|s-Triazinetriamine|1,5-Triazine-2,4,6-triamine|MELAMINE [IARC]|Pluragard|1,3,5-Triazine-2,4,6-triamine; Metformin Hydrochloride Imp. D (EP); Melamine; Metformin Imp. D (EP); Metformin Hydrochloride Impurity D; Metformin Impurity D|Metformin EP impurity D|[1,3,5]triazine-2,4,6-triamine|Cyanuramide|1,5-Triazine-2,4,6(1H,3H,5H)-triimine|DG 002|Melamine Monomer|4,6-Diamino-1,2-dihydro-2-imino-S-Triazine|Cyanuric triamide|MELAMINE|2,4, 6-Triamino-1,3,5-triazine|2,4,6-Triamino-1,3,5-triazine Monomer|Yukamelamine|ZS 27|Mark ZS 27|METFORMIN HYDROCHLORIDE IMPURITY D (EP IMPURITY)|MELAMINE [INCI]|1,3,5-triazine-2,4,6(1H,3H,5H)triimine|1,3,5-Triazine-2,4,6(1H,3H,5H)-triimine|1,3,5-triazinane-2,4,6-triimine|ADK Stab ZS 27|Hicophor PR|s-Triazine, 2,4,6-triamino-|1,3,5-Triazine-2,4,6-triamine (Melamine)|2,4,6-Triamino-1,3,5-triazine|Cyanurotriamine|Cyanurtriamide|Cymel|AX2|Teoharn|Isomelamine|1,3,5-Triazine-2,4,6-triamine|Pluragard C 133|triamino-s-triazine|MELAMINE [HSDB]|METFORMIN HYDROCHLORIDE IMPURITY D [EP IMPURITY]|CYMEL (Salt/Mix)|Melamine-13C3,15N3|s-Triazine, 4,6-diamino-1,2-dihydro-2-imino-|Virset 656-4|2,6-Triaminotriazine|2,4,6-Triamino-s-triazine|Aero|Cyanurotriamide|1,3,5-Triazine-2,4,6-triamine monomer|2,6-Triamino-s-triazine|2,4,6-triamino sym-triazine|MELAMINE [MI]

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Overview

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.

Specifications

Synonyms

MELAMINE (IARC) | Melamine; 1,3,5-Triazine-2,4,6-triamine | 2,6-Triamino-1,3,5-triazine | s-Triazine,4,6-triamino- | sym-Triaminotriazine | Triaminotriazine | MELAMINE (USP-RS) | Spinflam ML 94M | s-triaminotriazine | DG 002 (amine) | melamin | MELAMINE [USP-RS] | s-Triazinetriamine | 1,5-Triazine-2,4,6-triamine | MELAMINE [IARC] | Plurag Show more

Specifications & Purity

10mM in DMSO

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

This product requires cold chain shipping. Ground and other economy services are not available.

Names and Identifiers

Pubchem Sid

528769150

Canonical Smiles

C1(=NC(=NC(=N1)N)N)N

IUPAC Name

1,3,5-triazine-2,4,6-triamine

InChIKey

JDSHMPZPIAZGSV-UHFFFAOYSA-N

INCHI

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

Isomeric SMILES

C1(=NC(=NC(=N1)N)N)N

WGK Germany

1

RTECS

OS0700000

Molecular Weight

126.12

Beilstein

124341

Reaxy-Rn

124341

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=124341&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Triazines
      • Subclass 1,3,5-triazines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Triazines
• Subclass: 1,3,5-triazines
• Intermediate Tree Nodes: Not available
• Direct Parent: 1,3,5-triazines
• Alternative Parents: Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: 1,3,5-triazine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as 1,3,5-triazines. These are compounds containing a triazine ring, which is a heterocyclic ring, similar to the six-member benzene ring but with three carbons replaced by nitrogen atoms, at ring positions 1, 3, and 5.
• External Descriptors: s-triazine

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Chemical and Physical Properties

• Sensitivity: Moisture sensitive.
• Flash Point(°F): 572 °F
• Flash Point(°C): 300 °C
• Melt Point(°C): >300°C
• Molecular Weight: 126.120 g/mol
• XLogP3: -1.400
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 0
• Exact Mass: 126.065 Da
• Monoisotopic Mass: 126.065 Da
• Topological Polar Surface Area: 117.000 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 63.300
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1