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Key Documents

901439

Sigma-Aldrich

Triethylphosphine solution

1.0 M in toluene

Synonym(s):

PEt3, Triethylphosphorous solution

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About This Item

Linear Formula:
(C2H5)3P
CAS Number:
Molecular Weight:
118.16
Beilstein:
969170
MDL number:
UNSPSC Code:
12352128
NACRES:
NA.22

Pricing and availability is not currently available.

form

liquid

Quality Level

reaction suitability

reagent type: ligand
reaction type: Arylations

concentration

1.0 M in toluene

density

0.857 g/mL

functional group

phosphine

SMILES string

CCP(CC)CC

InChI

1S/C6H15P/c1-4-7(5-2)6-3/h4-6H2,1-3H3

InChI key

RXJKFRMDXUJTEX-UHFFFAOYSA-N

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This Item
MAB8052ZMS1110MABN12
species reactivity

human

species reactivity

human

species reactivity

adenovirus-infected cells

species reactivity

human, mouse

antibody form

ascites fluid

antibody form

purified immunoglobulin

antibody form

purified antibody

antibody form

purified immunoglobulin

clone

2/6, monoclonal, 20/11, monoclonal

clone

20/11, monoclonal

clone

20/11, recombinant monoclonal

clone

G2-11, monoclonal

technique(s)

ELISA: suitable, immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable, immunofluorescence: suitable

technique(s)

ELISA: suitable, flow cytometry: suitable, immunofluorescence: suitable, immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable

technique(s)

flow cytometry: suitable, immunocytochemistry: suitable, immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable

technique(s)

ELISA: suitable, immunohistochemistry: suitable, western blot: suitable

shipped in

wet ice

shipped in

wet ice

shipped in

ambient

shipped in

wet ice

Application

Catalyst for:
  • Regioselective formation of alcohols from hydrocarbonylation of alkenes
  • Bronsted acid-assisted synthesis of dihydropyrones from aromatic aldehydes and allenoates
  • Silaboration of enynes
  • Conversion of phenylacetic acids to phenylacetonitriles of benzonitriles
  • Thermal decomposition of platinum and palladium naphthalenediyl
  • Asymmetrical Morita-Baylis-Hillman reaction
Offered as the toluene solution for more convenient handling, triethylphosphine is a valuable ligand for
  • Regioselective formation of alcohols from hydrocarbonylation of alkenes.
  • Bronsted acid-assisted synthesis of dihydropyrones from aromatic aldehydes and allenoates.
  • Silaboration of enynes.
  • Conversion of phenylacetic acids to phenylacetonitriles of benzonitriles.
  • Thermal decomposition of platinum and palladium naphthalenediyl.
  • Asymmetrical Morita-Baylis-Hillman reaction.

related product

Signal Word

Danger

Hazard Classifications

Aquatic Chronic 3 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Pyr. Liq. 1 - Repr. 2 - Skin Corr. 1B - STOT RE 2 - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

4.2 - Pyrophoric and self-heating hazardous materials

WGK

WGK 3

Flash Point(F)

44.6 °F

Flash Point(C)

7 °C


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