Triethylphosphine

Product Information

Molecular Formula:
C6H15P
Molecular Weight:
118.16
Description
Triethylphosphine is generally used as a ligand in the organometallic chemistry. It can be used in:• Synthesis of the tetrahedrally coordinated L3Fe-Nx complex with a terminal nitride group.• Synthesis of (PEt3)2Ni(η2-C14H10), a source of the reactive Ni(PEt3)2 moiety.• Synthesis of dinuclear rhodium complexes with triethyllphosphane bridges.
Synonyms
AURORA KA-1111; CYTOP(R) 320; TRIETHYLPHOSPHINE; (C2H5)3P; Phosphorus triethyl; tl409; triethylphosphane; Triethyl-phosphane
IUPAC Name
triethylphosphane
Canonical SMILES
CCP(CC)CC
InChI
InChI=1S/C6H15P/c1-4-7(5-2)6-3/h4-6H2,1-3H3
InChI Key
RXJKFRMDXUJTEX-UHFFFAOYSA-N
Boiling Point
127-128°C
Melting Point
-3°C
Flash Point
-4.0 °F - closed cup
Purity
95%
Density
0.802
Appearance
clear liquid
Application
Used in organic syntheses.
Storage
Flammables-area.
Refractive Index
n20/D 1.456 (lit.)

Safety Information

Hazards
H250 - H314
Precautionary Statement
P231 + P232 - P280 - P303 + P361 + P353 - P305 + P351 + P338 + P310 - P370 + P378

Computed Properties

XLogP3
1
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
3
Exact Mass
118.091137476 g/mol
Monoisotopic Mass
118.091137476 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
7
Formal Charge
0
Complexity
25.7
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-113735902-A C15 phosphine salt isomer and preparation method and application thereof 2021-10-11
CN-113816925-A A trematopsin 3 "-tert-butyl-4 '- (2-hydroxyethoxy) -4" -pyrrolidin-1-yl [1, 1'; process for preparing 3 ', 1' ] -terphenyl-4-carboxylic acid 2021-09-18
CN-113651743-A Preparation method of beta-carotene 2021-08-30
CN-113461539-A Method for preparing organic diamine from amino nitrile organic matter 2021-08-02
CN-113441166-A Nitrogen-phosphorus co-doped carbon-based cobalt catalyst, preparation method thereof and synthesis method of saturated aliphatic primary amine 2021-08-02
CN-113582853-A Method and device for preparing organic diamine from organic amide 2021-08-02
CN-113461948-A Flash rust prevention agent and preparation method and application thereof 2021-07-12
CN-113499799-A Application of alkylidene carbene ruthenium metal complex in hydrogen production by catalyzing hydrogen storage carrier 2021-06-23
CN-113321571-A Synthesis method of linear dihydric alcohol 2021-06-21
CN-113201016-A Preparation method of C15 phosphonium salt 2021-05-19

Literatures

PMID Publication Date Title Journal
23035689 2012-10-15 Syntheses and electronic properties of rhodium(III) complexes bearing a redox-active ligand Inorganic chemistry
22455750 2012-04-11 Dispersion energy enforced dimerization of a cyclic disilylated plumbylene Journal of the American Chemical Society
22192797 2011-12-22 Proteomic analysis of endothelial cold-adaptation BMC genomics
22052590 2011-12-09 Assembling phthalocyanine dimers through a platinum(II) acetylide linker Chemistry (Weinheim an der Bergstrasse, Germany)
21843342 2011-08-15 Comparison of genomic and proteomic data in recurrent airway obstruction affected horses using Ingenuity Pathway Analysis® BMC veterinary research
21619653 2011-05-27 A large, consistent plasma proteomics data set from prospectively collected breast cancer patient and healthy volunteer samples Journal of translational medicine
21533132 2011-04-20 Systems-scale analysis reveals pathways involved in cellular response to methamphetamine PloS one
21077686 2011-01-13 Organometallic anticancer compounds Journal of medicinal chemistry
22084690 2011-01-01 Proteomic Characterization of Cerebrospinal Fluid from Ataxia-Telangiectasia (A-T) Patients Using a LC/MS-Based Label-Free Protein Quantification Technology International journal of proteomics
21105691 2010-12-20 Substitution of the terminal chloride ligands of [Re(6)S(8)Cl(6)](4-) with triethylphosphine: photophysical and electrochemical properties of a new series of [Re(6)S(8)](2+) based clusters Inorganic chemistry
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Related Products

Online Inquiry
  • Verification code
USA
  • International:
  • US & Canada (Toll free):
  • Email:
  • Fax:
UK
  • Email:
Copyright © 2024 BOC Sciences. All rights reserved.
Top
Inquiry Basket