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Propargyl Bromide CAS 106-96-7 Purity >99.0% (GC) Factory

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of Propargyl Bromide (Stabilized with MgO) (CAS: 106-96-7) with high quality, commercial production. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com

Chemical Name Propargyl Bromide (Stabilized with MgO)
Synonyms 3-Bromopropyne; 3-Bromo-1-Propyne; PBr; (Stabilized with MgO)
CAS Number 106-96-7
CAT Number RF-PI1906
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C3H3Br
Molecular Weight 118.96
Melting Point -61℃
Boiling Point 90℃
Solubility Soluble in Ethanol, Benzene, Ether; Insoluble in Water
Brand Ruifu Chemical
Item Specifications
Appearance Colorless to Light Yellow Clear Liquid
Purity / Analysis Method >99.0% (GC)
Moisture (K.F) <0.20%
Stabilizer 0.3% MgO Conforms
Single Impurity <0.70%
Total Impurities <1.00%
Refractive Index N20/D 1.491~1.496
Specific Gravity (20/20℃) 1.578~1.600
Infrared Spectrum Conforms to Structure
Test Standard Enterprise Standard
Usage Pesticide Intermediate; Pharmaceutical Intermediates

Package: Fluorinated Bottle, 25kg/Drum, or according to customer's requirement

Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture

Propargyl Bromide (Stabilized with MgO), also known as 3-Bromopropyne, (CAS 618-89-3) is used in organic synthesis, is an intermediate of pyrethroid propynthrin, used in the synthesis of various acetylene derivatives; in the pharmaceutical industry for the manufacture of anti-fungal drug chloropropyne iodine. Used to make propargylic amines employed in enyne metathesis. Apply to soil pesticides and chemical intermediates. Propargyl Bromide is also used in the synthesis of betulonic acid-peptide conjugates with anti-inflammatory activity. Also used in the synthesis of PEG and peptide-grafted polyesters. Propargyl Bromide is highly flammable and a dangerous fire risk, sensitive to shock. 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.