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

CAS: 15715-58-9 Cat. No.: T466164 Formula: C₇H₁₇NO₃ Peso molecolare: 163.21 Numero EC: 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

Panoramica

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

Sinonimi

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

Specifiche e purezza

1.0M, pH 8.5±0.1

Meccanismi biochimici e fisiologici

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

Condizioni di conservazione di stoccaggio

Store at 2-8°C

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Nomi e identificatori

• Pubchem Sid: 508811442
• Sorrisi canonici: 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)
• Isomeri SMILES: CCN(CC)CC.C(=O)(O)O
• WGK Germania: 3
• PubChem CID: 3082099
• Peso molecolare: 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
• Descrizione: 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

Proprietà chimiche e fisiche

• Peso molecolare: 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

Riferimenti

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]