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Ethylmagnesium bromide

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Products Intro: Product Name:Ethylmagnesium bromide 3M ether solution
CAS:925-90-6
Purity:99% Package:25KG/Drum
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Products Intro: Product Name:Ethylmagnesium bromide
CAS:925-90-6
Purity:99.99% Package:1kg;100USD
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Products Intro: Product Name:Ethylmagnesium Bromide
CAS:925-90-6
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Products Intro: Product Name:ETHYLMAGNESIUM BROMIDE
CAS:925-90-6
Purity:99% Package:25KG
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Products Intro: Product Name:Ethylmagnesium Bromide
CAS:925-90-6
Purity:99.9% Package:1KG;30USD

Ethylmagnesium bromide manufacturers

  • Ethylmagnesium Bromide
  • Ethylmagnesium Bromide pictures
  • $30.00 / 1KG
  • 2024-01-04
  • CAS:925-90-6
  • Min. Order: 1KG
  • Purity: 99.9%
  • Supply Ability: 20 Tons
Ethylmagnesium bromide Basic information
Product Name:Ethylmagnesium bromide
Synonyms:ETHYLMAGNESIUM BROMIDE, CA. 3.2M SOLUTION IN 2-METHYLTETRAHYDROFURAN;Ethylmagnesium bromide, 0.9M solution in tert-butyl methyl ether;Ethylmagnesium bromide1M solution in THFAcroSeal§3;Ethylmagnesium bromide0.9M in tert-Butyl methyl ether;Ethylmagnesium bromide3M in Diethyl etherAcroSeal§3;Ethylmagnesium bromide, 3M in ether, packaged under Argon in resealable ChemSeal^t bottles;Ethylmagnesium Bromide (13% in Tetrahydrofuran, ca. 1mol/L);Ethylmagnesium bromide,ca. 3.2M solution in 2-Methyl-THF: AcroSeal(R)
CAS:925-90-6
MF:C2H5BrMg
MW:133.27
EINECS:213-127-3
Product Categories:Classes of Metal Compounds;Grignard Reagents;Grignard Reagents & Alkyl Metals;Mg (Magnesium) Compounds;Synthetic Organic Chemistry;Typical Metal Compounds;AlkylChemical Synthesis;Grignard Reagents;Organic Bases;Organometallic Reagents;Synthetic Reagents;Alkyl;Chemical Synthesis;Organometallic Reagents;grignard reagent;925-90-6
Mol File:925-90-6.mol
Ethylmagnesium bromide Structure
Ethylmagnesium bromide Chemical Properties
Melting point -116.3°C
Boiling point 34.6°C
density 1.02 g/mL at 25 °C
Fp <−30 °F
storage temp. water-free area
solubility Miscible in alcohols, ketones, esters, ethers, hydrocarbons.
form Solution
color Pale yellow to brown
Water Solubility Reacts with water.
Sensitive Air & Moisture Sensitive
BRN 3587203
Exposure limitsACGIH: TWA 400 ppm; STEL 500 ppm
OSHA: TWA 400 ppm(1200 mg/m3)
NIOSH: IDLH 1900 ppm
InChIInChI=1S/C2H5.BrH.Mg/c1-2;;/h1H2,2H3;1H;/q;;+1/p-1
InChIKeyTWTWFMUQSOFTRN-UHFFFAOYSA-M
SMILESC(C)[Mg]Br
CAS DataBase Reference925-90-6(CAS DataBase Reference)
EPA Substance Registry SystemMagnesium, bromoethyl- (925-90-6)
Safety Information
Hazard Codes F+,C,F
Risk Statements 12-14/15-19-22-34-66-67-40-11-14-37
Safety Statements 16-26-36/37/39-43-45-7/8-27-9
RIDADR UN 3399 4.3/PG 1
WGK Germany 1
1-3-10
TSCA Yes
HazardClass 4.3
PackingGroup I
HS Code 29319090
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Ethylmagnesium bromide Usage And Synthesis
Chemical PropertiesEthylmagnesium bromide is generally sold as a dark brown solution and can be dissolved in diethyl ether, butyl ether, isopropyl ether, THF and anisole.
UsesEthylmagnesium Bromide is a useful reagent in preparation of zirconium complexes having two phenoxy-imine chelate ligands for olefin polymerization.
PreparationEthylmagnesium bromide is commercially available, usually as a solution in diethyl ether or tetrahydrofuran. It may be prepared in the normal manner of Grignard reagents — by reacting bromoethane with magnesium in diethyl ether:
EtBr + Mg → EtMgBr
ReactionsEthylmagnesium bromide reacts with water to produce ethane.
CH3CH2MgBr+H2O→CH3-CH3+Mg(OH)Br
Reaction of ethylmagnesium bromide with ethyl acetate in the presence of styrene and titanium(IV) isopropoxide as a catalyst leads to (Z)-1-methyl-2-phenylcyclopropanol in 42% yield.
General DescriptionEthylmagnesium bromide, an organomagnesium compound, is commonly known as Grignard reagent. It is a powerful carbon nucleophile mainly used for C-C bond formation. Ethylmagnesium bromide solution (3.0 M in diethyl ether) can be used for copper(I)-catalyzed allylic substitution reaction.
Grignard reagents are organometallic compounds discovered by a French chemist, Victor Grignard in 1900. These compounds can be obtained as a formula “RMgX” by the reaction of halogenated hydrocarbons with magnesium metal in anhydrous solvents such as diethyl ether,1) and have been widely used in organic synthesis.
HazardFlammable, dangerous fire risk.
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