Triethylmethylammonium hydroxide solution - 20 wt. % in H2O , CAS No.109334-81-8

CAS: 109334-81-8 Cat. No.: T336968 Formule: C₇H₁₉NO Poids moléculaire: 133.23 Numéro CE: 600-911-9 PubChem CID: 14647552

GRADE & PURITY 20 wt. % in H2O

Synonyms

J-002271 | Methyltriethylammonium hydroxide | AKOS015913704 | N,N-Diethyl-N-methylethanaminium hydroxide | SCHEMBL188610 | DTXSID10562588

Storage

Room temperature

Shipped In

Normal

Vue d’ensemble

application：

Triethylmethylammonium hydroxide solution can be used:

To adjust the pH of the reaction mixture in the synthesis of H2VOPO4, which in turn is used to synthesize a vanadium phosphate named ε-VOPO4.

To prepare ionic liquids with amino acid anions, exhibiting bipolar solvent properties.

Specifications

Synonymes

J-002271 | Methyltriethylammonium hydroxide | AKOS015913704 | N,N-Diethyl-N-methylethanaminium hydroxide | SCHEMBL188610 | DTXSID10562588

Spécifications et pureté

20 wt. % in H2O

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Noms et identifiants

• Pubchem Sid: 488198710
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488198710
• Sourires canoniques: CC[N+](C)(CC)CC.[OH-]
• IUPAC Name: triethyl(methyl)azanium;hydroxide
• InChIKey: JAJRRCSBKZOLPA-UHFFFAOYSA-M
• INCHI: 1S/C7H18N.H2O/c1-5-8(4,6-2)7-3;/h5-7H2,1-4H3;1H2/q+1;/p-1
• Isomères SMILES: CC[N+](C)(CC)CC.[OH-]
• PubChem CID: 14647552
• Poids moléculaire: 133.23

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Classe Organonitrogen compounds
      • Subclass Quaternary ammonium salts

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Quaternary ammonium salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetraalkylammonium salts
• Alternative Parents: Organic salts Organic oxoanionic compounds Organic oxides Hydrocarbon derivatives Amines Organic cations
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetraalkylammonium salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organic hydroxide - Amine - Organic cation - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as tetraalkylammonium salts. These are organonitrogen compounds containing a quaternary ammonium substituted with four alkyl chains.
• 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

Propriétés chimiques et physiques

• Indice de réfraction: 1.373
• Point d'ébullition (°C): 102° C at 760 mmHg
• Poids moléculaire: 133.230 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 133.147 Da
• Monoisotopic Mass: 133.147 Da
• Topological Polar Surface Area: 1.000 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 47.100
• 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: 2

XLogP3

Références

1. Yang Wang, Lijuan Liu, Pan Chen, Lina Zhang, Ang Lu.  (2018)  Cationic hydrophobicity promotes dissolution of cellulose in aqueous basic solution by freezing–thawing.  PHYSICAL CHEMISTRY CHEMICAL PHYSICS,  20  (20): (14223-14233).  [PMID:29761185] [10.1039/C8CP01268G]

Foire aux questions

How should this product be stored?

Store at room temperature.

How is this product shipped?

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