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Ethyltriphenylphosphonium bromide, 98+%, Thermo Scientific Chemicals

$71.40 - $642.81

Chemical Identifiers

CAS 1530-32-1
Molecular Formula C20H20BrP
Molecular Weight (g/mol) 371.26
MDL Number MFCD00011838
InChI Key JHYNXXDQQHTCHJ-UHFFFAOYSA-M
Synonym ethyltriphenylphosphonium bromide, ethyl triphenyl phosphonium bromide, triphenylethylphosphonium bromide, phosphonium, ethyltriphenyl-, bromide, ethyltriphenylphosphanium bromide, ethyl triphenylphosphonium bromide, unii-r85v84ul5v, ethyltriphenylphosphoniumbromide, guaifenesin powder, pubchem18705
PubChem CID 73727
SMILES [Br-].CC[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
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Products 3
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAB2309614
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Thermo Scientific Chemicals
B2309614
25 g
Each for $71.40
 
AAB2309622
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Thermo Scientific Chemicals
B2309622
100 g
Each for $182.62
 
AAB2309636
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Thermo Scientific Chemicals
B2309636
500 g
Each for $642.81
 
Description

Description

Ethyltriphenylphosphonium bromide acts as a reactant in the synthesis of D-amino acids from L-cysteine-derived thiazolidines, Leiodolide A through aldol reactions and Horner-Wadsworth-Emmons olefination. It is also used in the preparation of cycloalkanoindolines through diastereoselective intramolecular inimo-ene reactions. Further, it is used as a reagent in solid-state metathesis polycondensation to prepare alkyl-dipropenylthiophene monomers and Mizoroki-Heck cyclization and cascading Tsuji-Trost cyclization reactions.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Ethyltriphenylphosphonium bromide acts as a reactant in the synthesis of D-amino acids from L-cysteine-derived thiazolidines, Leiodolide A through aldol reactions and Horner-Wadsworth-Emmons olefination. It is also used in the preparation of cycloalkanoindolines through diastereoselective intramolecular inimo-ene reactions. Further, it is used as a reagent in solid-state metathesis polycondensation to prepare alkyl-dipropenylthiophene monomers and Mizoroki-Heck cyclization and cascading Tsuji-Trost cyclization reactions.

Solubility
Soluble in methanol. Slightly soluble in water, acetone and isopropanol.

Notes
Hygroscopic. Incompatible with oxidizing agents.
Specifications

Chemical Identifiers

1530-32-1
371.26
JHYNXXDQQHTCHJ-UHFFFAOYSA-M
73727
C20H20BrP
MFCD00011838
ethyltriphenylphosphonium bromide, ethyl triphenyl phosphonium bromide, triphenylethylphosphonium bromide, phosphonium, ethyltriphenyl-, bromide, ethyltriphenylphosphanium bromide, ethyl triphenylphosphonium bromide, unii-r85v84ul5v, ethyltriphenylphosphoniumbromide, guaifenesin powder, pubchem18705
[Br-].CC[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1

Specifications

1530-32-1
>200°C (392°F)
C20H20BrP
MFCD00011838
UN3077
Hygroscopic
Soluble in methanol. Slightly soluble in water,acetone and isopropanol.
[Br-].CC[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
371.26
371.26
Ethyltriphenylphosphonium bromide
206°C to 210°C
Odorless
CH3CH2P(C6H5)3Br
25 g
3599630
ethyltriphenylphosphonium bromide, ethyl triphenyl phosphonium bromide, triphenylethylphosphonium bromide, phosphonium, ethyltriphenyl-, bromide, ethyltriphenylphosphanium bromide, ethyl triphenylphosphonium bromide, unii-r85v84ul5v, ethyltriphenylphosphoniumbromide, guaifenesin powder, pubchem18705
JHYNXXDQQHTCHJ-UHFFFAOYSA-M
ethyl(triphenyl)phosphanium;bromide
73727
≥98%
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Safety and Handling

Safety and Handling

GHS H Statement
H302-H312-H315-H319-H335
Harmful if swallowed.
Harmful in contact with skin.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P264b-P270-P280i-P301+P310-P305+P351+P338-P330-P501c

H301-H319-H500

DOTInformation : Hazard Class: 6.1; Packaging Group: III

EINECSNumber : 216-223-3

TSCA : Yes

Recommended Storage : Ambient temperatures; Store under Nitrogen

SDS
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RUO – Research Use Only