Sodium Thiomethoxide

95%

Reagent Code: #235337
label
Alias Sodium methyl thiol, methanethiol Sodium salt, sodium methyl thiol
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CAS Number 5188-07-8

science Other reagents with same CAS 5188-07-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 70.09(anhy) g/mol
Formula CH₃NaS·xH₂O
badge Registry Numbers
MDL Number MFCD00174316
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a strong nucleophile in organic synthesis, particularly in the preparation of sulfides and thioethers through alkylation reactions. Commonly employed in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) where sulfur-containing functional groups are required. Also utilized in the production of agrochemicals and dyes due to its ability to introduce methylthio groups efficiently. Acts as a reagent in the modification of peptides and nucleic acids in research settings. Requires careful handling due to its moisture sensitivity and potential for releasing toxic gases upon decomposition.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,980.00
inventory 5g
10-20 days ฿6,680.00
inventory 25g
10-20 days ฿26,280.00
inventory 100g
10-20 days ฿89,000.00

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Sodium Thiomethoxide
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Used as a strong nucleophile in organic synthesis, particularly in the preparation of sulfides and thioethers through alkylation reactions. Commonly employed in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) where sulfur-containing functional groups are required. Also utilized in the production of agrochemicals and dyes due to its ability to introduce methylthio groups efficiently. Acts as a reagent in the modification of peptides and nucleic acids in research s

Used as a strong nucleophile in organic synthesis, particularly in the preparation of sulfides and thioethers through alkylation reactions. Commonly employed in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) where sulfur-containing functional groups are required. Also utilized in the production of agrochemicals and dyes due to its ability to introduce methylthio groups efficiently. Acts as a reagent in the modification of peptides and nucleic acids in research settings. Requires careful handling due to its moisture sensitivity and potential for releasing toxic gases upon decomposition.

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