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

CAS: 108-78-1 Cat. No.: M420556 Fórmula: C₃H₆N₆ Peso molecular: 126.12 Beilstein Registry Number: 124341 Número CE: 203-615-4

GRAU & PUREZA 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

Visão geral

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.

Especificações

Sinónimos

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

Especificações e pureza

10mM in DMSO

Condições de armazenamento de armazenamento

Store at -80°C

Enviado em

Dry ice packs + Cold packs

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Nomes e identificadores

Pubchem Sid

528769150

Sorrisos canónicos

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)

SMILES isoméricas

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

WGK Alemanha

1

RTECS

OS0700000

Peso molecular

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
    • Classe Triazines
      • Subclass 1,3,5-triazines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: 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
• Descrição: 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

Mecanismos de ação

Propriedades químicas e físicas

• Sensibilidade: Moisture sensitive.
• Ponto de inflamação (°F): 572 °F
• Ponto de inflamação (°C): 300 °C
• Ponto de fusão (°C): >300°C
• Peso molecular: 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