Triethylamine - Standard for GC, ≥99.5%(GC) , CAS No.121-44-8

CAS: 121-44-8 Cat. No.: T103284 分子式: C₆H₁₅N 分子量: 101.19 Beilstein Registry Number: 605283 EC番号: 204-469-4

GRADE & PURITY Standard for GC, ≥99.5%(GC)

Synonyms

triethyl amin | Triethylamine, for protein sequence analysis, ampule, >=99.5% (GC) | Triethylamine, United States Pharmacopeia (USP) Reference Standard | EINECS 204-469-4 | N,N-Diethylethanamine | N,N-diethyl-ethanamine | triehyl amine | TRIETHYLAMINE [MI

Storage

Protected from light,Room temperature,Argon charged

Shipped In

FedEx DG Service

概要

Triethylamine has been used to bind the n-hydroxysuccinimide (NHS) group with the amino-treated tip surface. It has also been used as a basic catalyst for acylation.

Specifications

同義語

triethyl amin | Triethylamine, for protein sequence analysis, ampule, >=99.5% (GC) | Triethylamine, United States Pharmacopeia (USP) Reference Standard | EINECS 204-469-4 | N,N-Diethylethanamine | N,N-diethyl-ethanamine | triehyl amine | TRIETHYLAMINE [MI

仕様と純度

Standard for GC, ≥99.5%(GC)

生化学的・生理学的メカニズム

Triethylamine (TEA) may play a dual role as a base and a solubilizing agent for promoting the reaction in toluene and TEA. Triethylamine, a mobile-phase modifier, is used in the reversed-phase high-performance liquid chromatography (RP-HPLC) separation of

保管条件

Protected from light,Room temperature,Argon charged

入荷

FedEx DG Service

等級

Standard for GC

純度

≥99.5%(GC)

名前と識別子

• パブケム・シド: 508811452
• パブケム・シド・ウル: https://pubchem.ncbi.nlm.nih.gov/substance/508811452
• カノニカル・スマイル: CCN(CC)CC
• IUPAC Name: N,N-diethylethanamine
• InChIKey: ZMANZCXQSJIPKH-UHFFFAOYSA-N
• INCHI: 1S/C6H15N/c1-4-7(5-2)6-3/h4-6H2,1-3H3
• 異性体SMILES: CCN(CC)CC
• WGKドイツ: 1
• RTECS: YE0175000
• UN番号: 1296
• 包装グループ: II
• 分子量: 101.19
• Beilstein: 605283

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • 分類 Organonitrogen compounds
      • Subclass Amines
        • Level5 Tertiary amines
          • Level6 Trialkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• 分類: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Tertiary amines
• Direct Parent: Trialkylamines
• Alternative Parents: Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tertiary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
• 説明: This compound belongs to the class of organic compounds known as trialkylamines. These are organic compounds containing a trialkylamine group, characterized by exactly three alkyl groups bonded to the amino nitrogen.
• External Descriptors: tertiary amine

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

作用メカニズム

化学的性質と物理的性質

• 感度: Light sensitive.
• 屈折率: 1.4003
• 引火点（°F）: 12.2 °F
• 引火点（°C）: -11 °C
• 沸点（°C）: 89～90°C
• 融点（°C）: -115°C
• 分子量: 101.190 g/mol
• XLogP3: 1.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 101.12 Da
• Monoisotopic Mass: 101.12 Da
• Topological Polar Surface Area: 3.200 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 25.700
• 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