Methanol-d4 - ≥99.8 atom% D , CAS No.811-98-3

CAS: 811-98-3 Cat. No.: M102262 Summenformel: CD₃OD Molekulargewicht: 36.07 Beilstein Registry Number: 1733278 EG-Nummer: 212-378-6

QUALITÄT & REINHEIT ≥99.8 atom% D

Synonyms

((2)H3)methan((2)H)ol|Propyleneoxide|((2)H4)methanol|Deuterated methanol|METHANOL (D4)|HCFC-22|Methanol D4|Methyl-d3 alcohol d|Carbonic chloride|CHI3|Methyl-d3 alcohol-d, cont. 0.03 v/v% TMS|(2H4)Methanol|Methanol-d4|Methan-d3-ol-d|methyl-d3 alcohol-d|trideuterio deuteriooxy methane|Perdeuteromethanol|Tetradeuteromethanol|MeNO2|Methyl Alcohol-d4|trideuterio(deuteriooxy)methane|Halocarbon 23

Storage

Protected from light,Room temperature,Argon charged,Desiccated

Shipped In

Normal

Übersicht

Methanol-d4 can be used as a solvent in nuclear magnetic resonance spectroscopy analysis for the characterization of phenolic compounds separated from olive oil using high-performance liquid chromatography. Through the biotransformation of red yeast, vanillic acid and 4-hydroxy-3-methoxystyrene are formed.

Spezifikationen

Synonyme

((2)H3)methan((2)H)ol | Propyleneoxide | ((2)H4)methanol | Deuterated methanol | METHANOL (D4) | HCFC-22 | Methanol D4 | Methyl-d3 alcohol d | Carbonic chloride | CHI3 | Methyl-d3 alcohol-d, cont. 0.03 v/v% TMS | (2H4)Methanol | Methanol-d4 | Methan-d3-ol-d | methyl-d3 alcohol-d | trideuterio deuteriooxy methane | Perdeuteromethanol | Tet Show more

Spezifikationen & Reinheit

≥99.8 atom% D

Storage

Protected from light,Room temperature,Argon charged,Desiccated

Verschickt in

Normal

Reinheit

≥99.8 atom% D

Namen und Kennungen

Pubchem Sid

508813885

Kanonisches Lächeln

CO

IUPAC Name

trideuterio(deuteriooxy)methane

InChIKey

OKKJLVBELUTLKV-MZCSYVLQSA-N

INCHI

1S/CH4O/c1-2/h2H,1H3/i1D3,2D

Isomere SMILES

[2H]OC([2H])([2H])[2H]

WGK Deutschland

1

Alternative CAS-Nummer

67-56-1（Unlabeled）

UN-Nummer

UN1230

Verpackungsgruppe

II

Molekulargewicht

36.07

Beilstein

1733278

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Klasse Organooxygen compounds
      • Subclass Alcohols and polyols

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: Organooxygen compounds
• Subclass: Alcohols and polyols
• Intermediate Tree Nodes: Not available
• Direct Parent: Primary alcohols
• Alternative Parents: Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydrocarbon derivative - Primary alcohol - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as primary alcohols. These are compounds comprising the primary alcohol functional group, with the general structure RCOH (R=alkyl, aryl).
• External Descriptors: Not available

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

Chemische und physikalische Eigenschaften

• Löslichkeit: It is miscible in water, ethanol, ether, acetone and chloroform.
• Empfindlichkeit: Light and Moisture sensitive
• Brechungsindex: 1.326
• Flammpunkt (°F): 51.8 °F
• Flammpunkt (°C): 11°C
• Siedepunkt (°C): 65.4°C
• Schmelzpunkt (°C): -98°C
• Molekulargewicht: 36.066 g/mol
• XLogP3: -0.500
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 36.0513 Da
• Monoisotopic Mass: 36.0513 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 2
• Formal Charge: 0
• Complexity: 2.000
• Isotope Atom Count: 4
• 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