tert-Butyl chloride, 98+%, Thermo Scientific Chemicals
tert-Butyl chloride, 98+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

tert-Butyl chloride, 98+%, Thermo Scientific Chemicals

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Catalog number A13004.AU
also known as A13004-AU
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67.65
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Quantity:
1000 mL
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Price (USD)/ Each
67.65
Online exclusive
79.50 
Save 11.85 (15%)
Add to cart
tert-Butyl chloride, 98+%, Thermo Scientific Chemicals
Catalog numberA13004.AU
Price (USD)/ Each
67.65
Online exclusive
79.50 
Save 11.85 (15%)
-
Add to cart
Chemical Identifiers
CAS507-20-0
IUPAC Name2-chloro-2-methylpropane
Molecular FormulaC4H9Cl
InChI KeyNBRKLOOSMBRFMH-UHFFFAOYSA-N
SMILESCC(C)(C)Cl
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless
FormLiquid
Assay (GC)≥98.0%
Identification (FTIR)Conforms
Refractive Index1.3835-1.3875 @ 20?C
tert-Butyl chloride plays an important role as a starting material to perform nucleophilic substitution reactions in order to prepare alcohol and alkoxides salts. It is used as an alkylating agent for the introduction of tert-butyl group and is also involved in Friedel-Crafts reactions. It is employed as an intermediate for the synthesis of agrochemicals and pharmaceuticals.

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 chloride plays an important role as a starting material to perform nucleophilic substitution reactions in order to prepare alcohol and alkoxides salts. It is used as an alkylating agent for the introduction of tert-butyl group and is also involved in Friedel-Crafts reactions. It is employed as an intermediate for the synthesis of agrochemicals and pharmaceuticals.

Solubility
Miscible with alcohol, benzene, chloroform and ether. Slightly miscible with water.

Notes
Hygroscopic. Incompatible with strong oxidizing agents and strong bases.
RUO – Research Use Only

General References:

  1. Stathi, P.; Deligiannakis, Y.; Avgouropoulos, G.; Louloudi, M. Efficient H 2 production from formic acid by a supported iron catalyst on silica. Appl. Catal., A 2015, 498, 176-184
  2. Sedov, I. A.; Stolov, M. A.;Solomonov, B. N. tert-Butyl chloride as a probe of the solvophobic effects. Fluid Phase Equilib. 2014, 382 164-168.