2-Bromo-N,N-dimethylethylamine hydrobromide - ≥95% , CAS No.2862-39-7

CAS: 2862-39-7 Cat. No.: B183437 Formula: C₄H₁₀BrN.BrH Peso molecolare: 232.9 Numero EC: 220-680-4 PubChem CID: 45791347

GRADE & PURITY ≥95%

Synonyms

AM84884 | Ethanamine, 2-bromo-N,N-dimethyl-, hydrobromide | Ethanamine, 2-bromo-N,N-dimethyl-, hydrobromide (1:1) | GS-4522 | M0735 | A876676 | Dimethylaminoethyl bromide hydrobromide | SCHEMBL28116 | 2-Bromo-N,N-dimethylethan-1-amine--hydrogen bromide (1

Storage

Room temperature

Shipped In

Normal

Specifications

Sinonimi

AM84884 | Ethanamine, 2-bromo-N,N-dimethyl-, hydrobromide | Ethanamine, 2-bromo-N,N-dimethyl-, hydrobromide (1:1) | GS-4522 | M0735 | A876676 | Dimethylaminoethyl bromide hydrobromide | SCHEMBL28116 | 2-Bromo-N,N-dimethylethan-1-amine--hydrogen bromide (1

Specifiche e purezza

≥95%

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Purezza

≥95%

Nomi e identificatori

• Pubchem Sid: 488201254
• Sorrisi canonici: CN(C)CCBr.Br
• IUPAC Name: 2-bromo-N,N-dimethylethanamine;hydrobromide
• InChIKey: MFRUVSDIZTZFFL-UHFFFAOYSA-N
• INCHI: 1S/C4H10BrN.BrH/c1-6(2)4-3-5;/h3-4H2,1-2H3;1H
• Isomeri SMILES: CN(C)CCBr.Br
• PubChem CID: 45791347
• Peso molecolare: 232.9

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Tertiary amines
• Direct Parent: Trialkylamines
• Alternative Parents: Organopnictogen compounds Organobromides Organic bromide salts Hydrocarbon derivatives Alkyl bromides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tertiary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Organic bromide salt - Organic salt - Organobromide - Organohalogen compound - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound
• Descrizione: 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: 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

Proprietà chimiche e fisiche

• Peso molecolare: 232.940 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 232.924 Da
• Monoisotopic Mass: 230.926 Da
• Topological Polar Surface Area: 3.200 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 28.700
• 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: 2

XLogP3

Riferimenti

1. Jingjing Guo, Ailian Wang, Wenxi Ji, Taoyi Zhang, Haolin Tang, Haining Zhang.  (2021)  Protic ionic liquid-grafted polybenzimidazole as proton conducting catalyst binder for high-temperature proton exchange membrane fuel cells.  POLYMER TESTING,      [PMID:] [10.1016/j.polymertesting.2021.107066]

2. Zena Chen, Zhihang Liao, Fangning Du, Xiang Che, Likun Wang, Wei Shi, Changmin Yu, Naidi Yang.  (2025)  One-Step Facile Synthesis of a Cationic Photosensitizer with Electrostatic Anchoring of Bacteria for Photodynamic Therapy of MRSA-Infected Wounds.  ACS Applied Materials & Interfaces,      [PMID:41448952] [10.1021/acsami.5c18942]

Domande frequenti

How is this product shipped?

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