Thermo Scientific Chemicals

Propargyl bromide, 80% in toluene, stab. with MgO, Thermo Scientific Chemicals

Catalog number: A16580.AD
50 mL, Each
Thermo Scientific Chemicals

Propargyl bromide, 80% in toluene, stab. with MgO, Thermo Scientific Chemicals

Catalog number: A16580.AD
50 mL, Each
Quantity
Informational:Informational:This chemical may require us to obtain additional information for our regulatory and chemical compliance records. If required, we will contact you for this information once your order is placed.
Catalog number: A16580.AD
also known as A16580-AD
Price (USD)
Price: 97.00
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Chemical Identifiers

CAS
106-96-7
IUPAC Name
3-bromoprop-1-yne
Molecular Formula
C3H3Br
InChI Key
YORCIIVHUBAYBQ-UHFFFAOYSA-N
SMILES
BrCC#C
Appearance (Color)
Clear, colorless to pale yellow to yellow-orange
Refractive Index
1.4910-1.4970 @ 20?C
Assay (GC)
≥96.0% (excluding toluene)
Assay (Titration ex Bromide)
75-85% w/w product in toluene
Comment
May be hazy or contain sediment which is MgO stabilizer.

Description

Propargyl bromide, 80% in toluene is used to prepare betulonic acid-peptide conjugates with anti-inflammatory activity and propargylic amines employed in enyne metathesis. It finds application in the propargylation of spiro ketones, allylic alcohols and enone complexes. In Barbier-type reaction, it reacts with aldehydes to give alkyne alcohols. It is actively involved in the synthesis of polyethylene glycol (PEG) and peptide-grafted polyesters.

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
Propargyl bromide, 80% in toluene is used to prepare betulonic acid-peptide conjugates with anti-inflammatory activity and propargylic amines employed in enyne metathesis. It finds application in the propargylation of spiro ketones, allylic alcohols and enone complexes. In Barbier-type reaction, it reacts with aldehydes to give alkyne alcohols. It is actively involved in the synthesis of polyethylene glycol (PEG) and peptide-grafted polyesters.

Solubility
Miscible with ethanol, ether, benzene, carbon tetrachloride and chloroform. Immiscible with water.

Notes
Light sensitive. Store in a cool place. Incompatible withbases, strong oxidizing agents, copper, peroxides, silver, silver oxides, mercury and mercury oxides.
WARNING: Reproductive Harm - www.P65Warnings.ca.gov
RUO – Research Use Only

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