tert-Butyl nitrite, tech. 90%
tert-Butyl nitrite, tech. 90%
tert-Butyl nitrite, tech. 90%
Thermo Scientific Chemicals

tert-Butyl nitrite, tech. 90%

CAS: 540-80-7 | C4H9NO2 | 103.121 g/mol
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Quantity:
25 g
100 g
Catalog number L16135.14
also known as L16135-14
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Quantity:
25 g
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Specifications
Beilstein1209339
CAS540-80-7
Chemical Name or Materialtert-Butyl nitrite
DOT InformationTransport Hazard Class: 3; Packing Group: II; Proper Shipping Name: BUTYL NITRITES
Density0.867
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tert-Butyl nitrite is employed as a reagent for diazotization and nitrosation of alcohols, thiols, amines and cycloalkanes. It plays an important role in photocatalyzed conversion of aryl and heteroarylamines to selenides. It finds application in the preparation of aryl azides from aryl amines. It is also useful for radical multifunctionalization reactions of aliphatic alkenes and source of nitric oxide.

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
tert-Butyl nitrite is employed as a reagent for diazotization and nitrosation of alcohols, thiols, amines and cycloalkanes. It plays an important role in photocatalyzed conversion of aryl and heteroarylamines to selenides. It finds application in the preparation of aryl azides from aryl amines. It is also useful for radical multifunctionalization reactions of aliphatic alkenes and source of nitric oxide.

Solubility
Miscible with diethyl ether, chloroform, alcohol and carbon disulfide. Slightly miscible with water. Immiscible with glycerol.

Notes
Light sensitive. Store in cool place. Incompatible with strong reducing agents, powdered metals and strong acids.
RUO – Research Use Only

General References:

  1. Reagent for non-aqueous nitrosation and diazotization reactions; cf Isopentyl nitrite, L13909, and Isobutyl nitrite, L05259.
  2. Aromatic amines have been converted in good yields to aryl halides in the presence of the Cu(II) halide: J. Org. Chem., 42, 2426 (1977); 45, 2570 (1980).
  3. Zhao, J.; Li, P.; Xia, C.; Li, F. Metal-free regioselective C-3 nitration of quinoline N-oxides with tert-butyl nitrite. RSC Adv. 2015, 5 (41), 32835-32838.
  4. Monir, K.; Ghosh, M.; Jana, S.; Mondal, P.; Majee, A.; Hajra, A. Regioselective synthesis of nitrosoimidazoheterocycles using tert-butyl nitrite. Org. Biomol. Chem. 2015, 13 (32), 8717-8722.