N-Methyl-D-glucamine - ≥99% , CAS No.6284-40-8

CAS: 6284-40-8 Cat. No.: M106762 Formula: C₇H₁₇NO₅ Peso molecolare: 195.21 Beilstein Registry Number: 385906 Numero EC: 228-506-9

GRADE & PURITY ≥99%

Synonyms

Z1255485274 | 6HG8UB2MUY | A834035 | Meglumine 100 microg/mL in Acetonitrile | CAS-6284-40-8 | Meglumine (JP17/USP/INN) | MEGLUMINE [II] | AB00430469-03 | Meglumine, Pharmaceutical Secondary Standard; Certified Reference Material | Megluminum [INN-Latin]

Storage

Room temperature,Argon charged

Shipped In

Normal

Panoramica

N-Methyl-D-glucamine, also known as methylglucamine, is an organic compound that belongs to the class of amino sugars. It is commonly used in pharmaceutical and biochemical applications as a resolving and buffering agent. Salts of N-methyl-D-glucamine have also been used for X-ray contrast media and nuclear imaging agents.

Specifications

Sinonimi

Z1255485274 | 6HG8UB2MUY | A834035 | Meglumine 100 microg/mL in Acetonitrile | CAS-6284-40-8 | Meglumine (JP17/USP/INN) | MEGLUMINE [II] | AB00430469-03 | Meglumine, Pharmaceutical Secondary Standard; Certified Reference Material | Megluminum [INN-Latin]

Specifiche e purezza

≥99%

Applicazione

N-Methyl-D-glucamine (NMG) can be used as a reactant to prepare water-soluble polymer for the selective removal of arsenic from aqueous water. It is also used in the development of various resins and gels containing NMG to remove different oxyanions.

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged

Spedito in

Normal

Purezza

≥99%

Nomi e identificatori

• Pubchem Sid: 488180831
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180831
• Sorrisi canonici: CNCC(C(C(C(CO)O)O)O)O
• IUPAC Name: (2R,3R,4R,5S)-6-(methylamino)hexane-1,2,3,4,5-pentol
• InChIKey: MBBZMMPHUWSWHV-BDVNFPICSA-N
• INCHI: 1S/C7H17NO5/c1-8-2-4(10)6(12)7(13)5(11)3-9/h4-13H,2-3H2,1H3/t4-,5+,6+,7+/m0/s1
• Isomeri SMILES: CNC[C@@H]([C@H]([C@@H]([C@@H](CO)O)O)O)O
• WGK Germania: 3
• CAS alternativo: 90191-92-7
• Peso molecolare: 195.21
• Beilstein: 385906
• Reaxy-Rn: 2324336
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2324336&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Monosaccharides
          • Level6 Hexoses

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Monosaccharides
• Direct Parent: Hexoses
• Alternative Parents: 1,3-aminoalcohols Secondary alcohols 1,2-aminoalcohols Polyols Dialkylamines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hexose monosaccharide - 1,3-aminoalcohol - Secondary alcohol - 1,2-aminoalcohol - Secondary amine - Polyol - Secondary aliphatic amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary alcohol - Organonitrogen compound - Amine - Alcohol - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity.
• External Descriptors: secondary amino compound - hexosamine

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

Obiettivi associati (umani)

ADRB1 Tclin Adrenergic receptor beta (1214 Activities)

Discover Target: ADRB1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Obiettivi associati (non umani)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in water.
• Sensibilità: Air & Moisture sensitive
• Rotazione specifica [α]: -16.5 ° (C=2, H2O)
• Punto di ebollizione (°C): 210 °C/1013 hPa
• Punto di fusione (°C): 129-131.5 °C (lit.)
• Peso molecolare: 195.210 g/mol
• XLogP3: -2.800
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 6
• Exact Mass: 195.111 Da
• Monoisotopic Mass: 195.111 Da
• Topological Polar Surface Area: 113.000 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 134.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 4
• 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

Domande frequenti

What is the purity of this product?

This product is supplied at ≥99% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at room temperature under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 6284-40-8, the molecular formula is C7H17NO5, and the molecular weight is 195.21 g/mol. InChIKey MBBZMMPHUWSWHV-BDVNFPICSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.