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

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

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Catalog number A16580.AK
also known as A16580-AK
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Quantity:
250 mL
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Price (USD)/ Each
358.65
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Ends: 31-Dec-2024
422.00 
Save 63.35 (15%)
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Propargyl bromide, 80% in toluene, stab. with MgO, Thermo Scientific Chemicals
Catalog numberA16580.AK
Price (USD)/ Each
358.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
422.00 
Save 63.35 (15%)
-
Add to cart
Chemical Identifiers
CAS106-96-7
IUPAC Name3-bromoprop-1-yne
Molecular FormulaC3H3Br
InChI KeyYORCIIVHUBAYBQ-UHFFFAOYSA-N
SMILESBrCC#C
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear, colorless to pale yellow to yellow-orange
Refractive Index1.4910-1.4970 @ 20?C
Assay (GC)≥96.0% (excluding toluene)
Assay (Titration ex Bromide)75-85% w/w product in toluene
CommentMay be hazy or contain sediment which is MgO stabilizer.
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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

General References:

  1. Li, Y.; Cheng, B. One-pot synthesis of precise polyisoxazoles by click polymerization: Copper (I)-catalyzed 1, 3-dipolar cycloaddition of nitrile oxides with alkynes. J. Polym. Sci. A Polym. Chem. 2013, 51 (7), 1645-1650.
  2. Un, I.; Ibisoglu, H.; Un, S. S.; Cosut, B.; Kılıc, A. Syntheses, characterizations, thermal and photophysical properties of cyclophosphazenes containing adamantane units. Inorg. Chim. Acta 2013, 399, 219-226.