2-Chloroacetamide, 98+%
2-Chloroacetamide, 98+%
2-Chloroacetamide, 98+%
Thermo Scientific™

2-Chloroacetamide, 98+%

CAS: 79-07-2 | C2H4ClNO | 93.51 g/mol
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Quantity:
250 g
5000 g
Catalog number A15238.0I
also known as A15238-0I
Price (USD)
342.65
Online Exclusive
380.00
Save 37.35 (10%)
Each
Quantity:
5000 g
Request bulk or custom format
Price (USD)
342.65
Online Exclusive
380.00
Save 37.35 (10%)
Each
Chemical Identifiers
CAS79-07-2
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White
FormCrystalline powder
Assay (HPLC)>98.0%

2-Chloroacetamide is used as surface-active agent in home laundry, cleaning products & household formulated cleaners, other industrial uses, petroleum production, polymer processing.

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
2-Chloroacetamide is used as surface-active agent in home laundry, cleaning products & household formulated cleaners, other industrial uses, petroleum production, polymer processing.

Solubility
Soluble in water(90g/L).

Notes
Store in cool, dry conditions in well sealed containers. Keep container tightly closed.
RUO – Research Use Only

General References:

  1. Harald Mollendal.; Svein Samdal. Conformation and Intramolecular Hydrogen Bonding of 2-Chloroacetamide as Studied by Microwave Spectroscopy and Quantum Chemical Calculations. J. Phys. Chem. A. 2006, 110, (6), 2139-2146.
  2. Jun-Min Liu.; Jian-Hua Bu.; Qi-Yu Zheng.; Chuan-Feng Chen.; Zhi-Tang Huang. Highly selective fluorescent sensing of Pb2+ by a new calix[4]arene derivative. Tetrahedron Letters. 2006, 47, (12), 1905-1908.
  3. N-Protected amino acids can be converted to carboxamidomethyl (CAM) esters via their Cs salts. The CAM protecting group can be cleaved under mildly basic conditions, but is stable to the conditions used for the cleavage of t-butyl, Boc, Fmoc or Cbz protecting groups: Tetrahedron Lett., 24, 5219 (1983). See Appendix 6.