Triethylammonium bicarbonate buffer - 1.0M, pH 8.5±0.1 , CAS No.15715-58-9

CAS: 15715-58-9 Cat. No.: T466164 Fórmula: C₇H₁₇NO₃ Peso molecular: 163.21 Número CE: 682-457-1 PubChem CID: 3082099

GRADE & PURITY 1.0M, pH 8.5±0.1

Synonyms

Triethylammonium bicarbonate buffer, 1 M, for HPLC | BS-21566 | DTXSID70935618 | Triethylammonium bicarbonate buffer, 1.0 M, pH 8.5+/-0.1 | AKOS015951101 | Triethylammonium bicarbonate buffer, volatile buffer, ~1.0 M in H2O | triethylamine carbonate | Car

Storage

Store at 2-8°C

Shipped In

Wet ice

Visão geral

Description

Triethylammonium bicarbonate buffer is used in ion-exchange chromatography and electrophoresis.It has also been used:in trypsin digestionas a component of lysis bufferto adjust the pH of buffer for protein quantificationBuffer for use in ion-exchange chromatography and electrophoresis.

Specifications

Sinónimos

Triethylammonium bicarbonate buffer, 1 M, for HPLC | BS-21566 | DTXSID70935618 | Triethylammonium bicarbonate buffer, 1.0 M, pH 8.5+/-0.1 | AKOS015951101 | Triethylammonium bicarbonate buffer, volatile buffer, ~1.0 M in H2O | triethylamine carbonate | Car

Especificações e pureza

1.0M, pH 8.5±0.1

Mecanismos bioquímicos e fisiológicos

Triethylammonium bicarbonate buffer is useful in oligonucleotides purification for electrospray mass spectrometry analysis. It is also utilized in trypsin digestion buffers.

Condições de armazenamento de armazenamento

Store at 2-8°C

Enviado em

Wet ice

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Nomes e identificadores

• Pubchem Sid: 508811442
• Sorrisos canónicos: CCN(CC)CC.C(=O)(O)O
• IUPAC Name: carbonic acid;N,N-diethylethanamine
• InChIKey: AFQIYTIJXGTIEY-UHFFFAOYSA-N
• INCHI: 1S/C6H15N.CH2O3/c1-4-7(5-2)6-3;2-1(3)4/h4-6H2,1-3H3;(H2,2,3,4)
• SMILES isoméricas: CCN(CC)CC.C(=O)(O)O
• WGK Alemanha: 3
• PubChem CID: 3082099
• Peso molecular: 163.21

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Organic carbonic acids and derivatives
      • Subclass Organic carbonic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Organic carbonic acids and derivatives
• Subclass: Organic carbonic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic carbonic acids
• Alternative Parents: Trialkylamines Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Not available
• Substituents: Tertiary aliphatic amine - Tertiary amine - Carbonic acid - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as organic carbonic acids. These are compounds comprising the carbonic acid functional group.
• 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

Propriedades químicas e físicas

• Peso molecular: 163.210 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 163.121 Da
• Monoisotopic Mass: 163.121 Da
• Topological Polar Surface Area: 60.800 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 51.900
• 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

Referências

1. Ningning Zhai, Shanshan Xu, Zongpu Qiu, Jingwen Cheng, Yuqing Sun, Zirui Wang, Shuying Han, Hao Wu, Rui Liu, Fen Zhang, Yuanqing Wei.  (2026)  Gradient-Decalcified Cuttlebone Powder-Loaded Hierarchical Microneedles: A Synergistic Therapeutic Strategy for Remodeling the Diabetic Wound.  Advanced Healthcare Materials,      [PMID:42473021] [10.1002/adhm.71455]

2. Xiaozheng Huang, Wanglin Bao, Shengming Tang, Miao Li, Yuqing Sun, Hui Ge, Yuxin Zhao, Hao Yuan, Xinyu Pan, Wei Lin, Yuanqing Wei, Shuying Han, Wenxing Wu, Rui Liu, Jin-ao Duan.  (2026)  Keratin utilizes H2S to promote HMGB1 sulfhydration for inflammation resolution.  Redox Biology,      [PMID:42546418] [10.1016/j.redox.2026.104326]

3. Yuchen Huang, Lexuan Hou, Lin Zhu, Xi Yang, Gang Li.  (2026)  Protocol for covalent ligand discovery via library-versus-proteome screening.  STAR Protocols,  7  (3): (104786).  [PMID:] [10.1016/j.xpro.2026.104786]