Triethylammonium bicarbonate buffer - UltraPureChrom™, for HPLC, 1M , CAS No.15715-58-9

CAS: 15715-58-9 Cat. No.: T466075 Summenformel: C₇H₁₇NO₃ Molekulargewicht: 163.21 EG-Nummer: 682-457-1 PubChem CID: 3082099

GRADE & PURITY UltraPureChrom™, for HPLC, 1M

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

Übersicht

Triethylammonium bicarbonate buffer is a commonly used chromatographic eluent, volatile buffer, mobile phase and ion-pairing agent for the purification of nucleic acids and biomolecules.Triethylammonium bicarbonate (TEAB) buffer may be used for studying proteins or noncovalent protein macromolecular complexes under “nondenaturing” conditions by electrospray ionization.Buffer for use in ion-exchange chromatography and electrophoresis.

Specifications

Synonyme

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

Spezifikationen & Reinheit

UltraPureChrom™, for HPLC, 1M

Storage

Store at 2-8°C

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Note

for HPLC, UltraPureChrom™

Namen und Kennungen

• Kanonisches Lächeln: 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)
• Isomere SMILES: CCN(CC)CC.C(=O)(O)O
• WGK Deutschland: 3
• PubChem CID: 3082099
• Molekulargewicht: 163.21

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: 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
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Molekulargewicht: 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

Referenzen

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]