Triethyl borate(TEB) - ≥97%(T) , CAS No.150-46-9

CAS: 150-46-9 Cat. No.: T104054 Formule: C₆H₁₅BO₃ Poids moléculaire: 145.99 Beilstein Registry Number: 1699052 Numéro CE: 205-760-9 PubChem CID: 9009

GRADE & PURITY ≥97%(T)

Synonyms

Q417816 | Triethylborat | 4-01-00-01365 (Beilstein Handbook Reference) | Borane, triethoxy- | Boric acid (H3BO3), triethyl ester | Boric acid (H3-BO3), triethyl ester | FT-0623168 | Ethyl borate | Tox21_303940 | TRIETHYL BORATE | BORON ETHOXIDE (B(OET)3)

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Vue d’ensemble

Application

Triethyl borate may be used as boron source to synthesize lithium borophosphates, alumina borosilicate ceramic nanofibres and boron-doped single wall carbon nanotubes.

Specifications

Synonymes

Q417816 | Triethylborat | 4-01-00-01365 (Beilstein Handbook Reference) | Borane, triethoxy- | Boric acid (H3BO3), triethyl ester | Boric acid (H3-BO3), triethyl ester | FT-0623168 | Ethyl borate | Tox21_303940 | TRIETHYL BORATE | BORON ETHOXIDE (B(OET)3)

Spécifications et pureté

≥97%(T)

Conditions de stockage de stockage

Room temperature,Argon charged

Expédié en

FedEx DG Service

Pureté

≥97%(T)

Noms et identifiants

Pubchem Sid

504751779

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504751779

Sourires canoniques

B(OCC)(OCC)OCC

IUPAC Name

triethyl borate

InChIKey

AJSTXXYNEIHPMD-UHFFFAOYSA-N

INCHI

1S/C6H15BO3/c1-4-8-7(9-5-2)10-6-3/h4-6H2,1-3H3

Isomères SMILES

B(OCC)(OCC)OCC

WGK Allemagne

2

RTECS

ED5075000

PubChem CID

9009

Numéro ONU

1176

Poids moléculaire

145.99

Beilstein

1699052

Reaxy-Rn

1699052

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organic oxoanionic compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organic oxoanionic compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic oxoanionic compounds
• Alternative Parents: Organic metalloid salts Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organic borate - Organic metalloid salt - Hydrocarbon derivative - Organic salt - Organooxygen compound - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as organic oxoanionic compounds. These are organic compounds containing an oxoanion.
• External Descriptors: borate esters

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

Propriétés chimiques et physiques

• Solubilité: Miscible with alcohol and ether.
• Sensibilité: Moisture sensitive
• Indice de réfraction: 1.3730 to 1.3770
• Point d'éclair (°F): 51.8 °F
• Point d'éclair (°C): 11℃
• Point d'ébullition (°C): 118°C
• Point de fusion (°C): -85°C(
• Poids moléculaire: 145.990 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 146.111 Da
• Monoisotopic Mass: 146.111 Da
• Topological Polar Surface Area: 27.700 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 55.700
• 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

XLogP3