tert-Butyl nitrite
90%
Reagent
Code: #122126
Alias
tert-butyl nitrite; tert-butyl nitrite
CAS Number
540-80-7
blur_circular Chemical Specifications
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Molecular Information
Weight
103.12 g/mol
Formula
C₄H₉NO₂
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Registry Numbers
EC Number
208-757-0
MDL Number
MFCD00002055
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Physical Properties
Boiling Point
61-63 °C(lit.)
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Storage & Handling
Density
0.867 g/mL at 25 °C(lit.)
Storage
2~8°C
description Product Description
Primarily used as a reagent in organic synthesis, it facilitates the formation of nitroso compounds and diazonium salts, which are essential intermediates in various chemical reactions. It is also employed in the production of pharmaceuticals, particularly in the synthesis of drugs that require nitrosation or diazotization steps. In industrial settings, it serves as a precursor for the preparation of rubber accelerators and corrosion inhibitors. Additionally, it has applications in analytical chemistry as a derivatizing agent for detecting amines and other nitrogen-containing compounds. Its use in recreational contexts, though illegal and dangerous, is noted for its vasodilatory effects.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (%) | 90-100% |
Refractive Index (N20/D) | 1.367-1.371 |
Solubility in Alcohol | Pass |
Appearance | Light Yellow Transparent Liquid |
Infrared Spectrum | Conforms To Structure |
Acid Value | 1.0 |
Water Content | 0.5 |
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tert-Butyl nitrite
Primarily used as a reagent in organic synthesis, it facilitates the formation of nitroso compounds and diazonium salts, which are essential intermediates in various chemical reactions. It is also employed in the production of pharmaceuticals, particularly in the synthesis of drugs that require nitrosation or diazotization steps. In industrial settings, it serves as a precursor for the preparation of rubber accelerators and corrosion inhibitors. Additionally, it has applications in analytical chemistry as a derivatizing agent for detecting amines and other nitrogen-containing compounds. Its use in recreational contexts, though illegal and dangerous, is noted for its vasodilatory effects.
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