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(Trimethylsilyl)diazomethane, 2M in hexanes, Thermo Scientific Chemicals

Catalog Number p-7029297
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Quantity:
5 mL
25 mL
100 mL
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18107-18-1
C4H10N2Si
114.223
MFCD00053946
ONDSBJMLAHVLMI-UHFFFAOYSA-N
trimethylsilyl diazomethane, trimethylsilyldiazomethane, diazomethyl trimethylsilane, tms-diazomethane, diazomethyl trimethyl silane, tmschn2, silane, diazomethyl trimethyl, unii-qi98hqo8c4, diazomethyl-trimethyl-silane, qi98hqo8c4
167693
diazomethyl(trimethyl)silane
C[Si](C)(C)C=[N+]=[N-]
This item is not returnable. View return policy
18107-18-1
C4H10N2Si
114.223
MFCD00053946
ONDSBJMLAHVLMI-UHFFFAOYSA-N
trimethylsilyl diazomethane, trimethylsilyldiazomethane, diazomethyl trimethylsilane, tms-diazomethane, diazomethyl trimethyl silane, tmschn2, silane, diazomethyl trimethyl, unii-qi98hqo8c4, diazomethyl-trimethyl-silane, qi98hqo8c4
167693
diazomethyl(trimethyl)silane
C[Si](C)(C)C=[N+]=[N-]

(Trimethylsilyl)diazomethane is used as a methylating agent in organic chemistry. It is utilized in Gas Chromatography- Mass-Spectrometry (GC-MS) for the analysis of various carboxylic compounds. It is involved as a reagent in the Doyle-Kirmse reaction with allyl sulfides and allyl amines. It is considered and used as a less-explosive replacement fordiazomethane. It is also used as a reactant for Unnatural alfa-amino acid derivatives containing gem-bisphosphonates through Michael addition reaction, imidazolo[2,1-b]benzothiazole derivatives and aigialomycin D analogues.

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
(Trimethylsilyl)diazomethane is used as a methylating agent in organic chemistry. It is utilized in Gas Chromatography- Mass-Spectrometry (GC-MS) for the analysis of various carboxylic compounds. It is involved as a reagent in the Doyle-Kirmse reaction with allyl sulfides and allyl amines. It is considered and used as a less-explosive replacement fordiazomethane. It is also used as a reactant for Unnatural alfa-amino acid derivatives containing gem-bisphosphonates through Michael addition reaction, imidazolo[2,1-b]benzothiazole derivatives and aigialomycin D analogues.

Solubility
Immiscible with water. Miscible with organic solvents.

Notes
(Trimethylsilyl)diazomethane (TMSD) in alcoholic solvents under acidic or basic conditions can lead to the formation of diazomethane. TMSD is under review by the National Toxicological Program for potential inhalation hazards.Incompatible with oxidizing agents, chlorine, fluorine and perchlorates.
TRUSTED_SUSTAINABILITY
Quantity 5 mL
UN Number UN3383
Beilstein 1902903
Flash Point −23°C (−10°F)
Solubility Information Immiscible with water. Miscible with organic solvents.
Formula Weight 114.22
Concentration or Composition (by Analyte or Components) 2M in hexanes
Sensitivity Light and moisture sensitive
Density 0.718
Chemical Name or Material (Trimethylsilyl)diazomethane

RUO – Research Use Only

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