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tert-Butyl isocyanate / 25 G

Purity: 97 %
Synonym: 2-isocyanato-2-methylpropane; Propane, 2-isocyanato-2-methyl-
Molecular Formula: (CH3)3CN'=C'=O
Molecular Weight: 99.13
SKU: MND-50267
CAS Number: 1609-86-5
MDL number: MFCD00002035
EC Number: 216-544-9
Form: liquid
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 25 G  
96.60 EUR



Safety Information


Hazard Statements

H225
H302
H335
H314
H317
H334
H330

Precautionary Statements

P210
P280
P303 + P361 + P353
P301 + P312
P305 + P351 + P338
P304 + P340 + P310

Pictograms



Properties

Signal WordDanger
Flash Point (C)-4 °C - closed cup
Flash Point (F)24.8 °F - closed cup
Density0.868 g/mL at 25 °C (lit.)
Boiling Point85-86 °C (lit.)

 Product Description

Tert-butyl isocyanate is a chemical compound commonly utilized in organic synthesis, specifically as a reagent for introducing isocyanate functionality into various molecules. Its application lies in the modification of organic compounds, serving as a key component in diverse chemical reactions.

 

Application:

Primarily used in organic synthesis, tert-butyl isocyanate acts as a reagent for the modification of organic compounds, facilitating the introduction of isocyanate functionality and contributing to various chemical reactions.

 

 

Articles:

- Reaction of tert-butyl isocyanate and tert-butyl isothiocyanate at the Ge(100) − 2 × 1 Surface

Publication Date: Available online 13 July 2010

Paul W. Loscutoff, Keith T. Wong, Stacey F. Bent

https://doi.org/10.1016/j.susc.2010.07.007

 

- Reactivity of Dimeric P/Al-Based Lewis Pairs toward Carbon Dioxide and tert-Butyl Isocyanate

Publication Date: June 14, 2013

Federica Bertini, Frank Hoffmann, Christian Appelt, Werner Uhl, Andreas W. Ehlers, J. Chris Slootweg and Koop Lammertsma

https://doi.org/10.1021/om3011382

 

- Nitrogen–Carbon Bond Formation by Reactions of a Titanium–Potassium Dinitrogen Complex with Carbon Dioxide, tert-Butyl Isocyanate, and Phenylallene

Publication Date: 05 June 2017

Yusuke Nakanishi, Dr. Yutaka Ishida, Prof. Dr. Hiroyuki Kawaguchi

https://doi.org/10.1002/ange.201704286