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 EC: 203-615-4
Disponible para pedir
CALIDAD & 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
★
Talla
Alemania (EU)
USA*
Precio
Cantidad
1ml
M420556-1ml
—
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51,11€

60,65€
Guardar 9,55 € (15.74%)
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Descripción general

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.

Especificaciones

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
Especificaciones y pureza
10mM in DMSO
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Pubchem Sid
Sonrisas canónicas
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)
Isómeros SMILES
C1(=NC(=NC(=N1)N)N)N
WGK Alemania
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=

Datos avanzados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseTriazines
Subclass1,3,5-triazines
Intermediate Tree Nodes Not available
Direct Parent1,3,5-triazines
Alternative Parents Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents 1,3,5-triazine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SensibilidadMoisture sensitive.
Punto de inflamación (°F)572 °F
Punto de inflamación (°C)300 °C
Punto de fusión (°C)>300°C
Peso molecular126.120 g/mol
XLogP3-1.400
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count0
Exact Mass126.065 Da
Monoisotopic Mass126.065 Da
Topological Polar Surface Area117.000 Ų
Heavy Atom Count9
Formal Charge0
Complexity63.300
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Determination of Additives in Beverages
How to Choose a Hydrogen Evolution (HER) Catalyst: Kinetic Barriers in Water Electrolysis, AWE/PEM/AEM Pathways, and a Materials-Family Roadmap (with a Product Map)
Triazine Compounds: Structural Features, Classification Logic, Typical Applications, and Key Considerations for Research Selection
Film Formation and Curing Mechanisms of Polyester Resins for Coatings: From Functional Groups and Curing Systems to Crosslinked Networks
VC/VAc Resins and Their Modification: An Analysis of VC/VAc Vinyl Resins for Coatings and Inks
Mechanisms and Control of Coating Yellowing: From Chromophoric Structure Formation to Source Diagnosis and Formulation Optimization
Structural Design Logic of Common Resin Modification Technologies: Molecular Chain Structure, Functional Groups, Phase Structure, Crosslinked Networks, and Hybrid/Functional Design
Resin Polarity in Coating Formulations: From Molecular Structure to Dissolution, Compatibility, Interfacial Interactions, and Formulation Design
Structure, Properties, and Mechanisms of Powdered Fragrances and Fragrance Delivery Materials: Stability, Release Mechanisms, and Selection Logic
Supramolecular Materials: From Molecular Recognition and Self-Assembly to Dynamic Function
Citations of This Product
Calculadoras de soluciones
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