79-07-2 Usage
Description
Chloroacetamide is a versatile chemical compound that serves as a preservative and surface-active agent in various applications. It is commonly used in cutting metalwork fluids, paints, glues, and as a leather preservative. However, it can induce contact dermatitis in certain individuals, such as hairdressers and shoemakers.
Uses
Used in Herbicidal Applications:
Chloroacetamide is a component of herbicidal mixtures that act as cellulose biosynthesis inhibitors, in combination with very-long-chain fatty acid (VLCFA) inhibitors. This helps control the growth of unwanted plants and contributes to effective weed management.
Used in Home and Industrial Cleaning:
2-Chloroacetamide is utilized as a surface-active agent in home laundry, cleaning products, and household formulated cleaners. Its surfactant properties enable it to break down dirt and stains, making it an essential component in these applications.
Used in Other Industrial Applications:
Chloroacetamide also finds use in various industrial processes, such as petroleum production and polymer processing. Its surface-active properties contribute to the efficiency and effectiveness of these processes.
Used as a Preservative in Cosmetics and Pharmaceuticals:
Chloroacetamide is employed as a preservative in cosmetic and pharmaceutical products, including creams, shampoos, and bath lotions. Its ability to inhibit the growth of microorganisms helps maintain the quality and safety of these products.
Used as a Preservative in Glues and Cooling Fluids:
In addition to its use in cosmetics and pharmaceuticals, chloroacetamide also serves as a preservative in glues and cooling fluids. It helps prevent the growth of microorganisms that could compromise the performance and longevity of these products.
Flammability and Explosibility
Nonflammable
Contact allergens
Chloroacetamide as a preservative is used in several
applications as in cutting metalworking fluids, in paints
or in glues. It can induce contact dermatitis in hairdressers
or in shoemakers, being used as a leather
preservative.
Safety Profile
Poison by ingestion,
intravenous, and intraperitoneal routes.
Mutation data reported. When heated to
decomposition it emits very toxic Cland
NOx. See also N-CHLOROACETAMIDE.
Purification Methods
Recrystallise the amide from acetone and dry it under vacuum over P2O5. [Beilstein 2 IV 490.]
Check Digit Verification of cas no
The CAS Registry Mumber 79-07-2 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79-07:
(4*7)+(3*9)+(2*0)+(1*7)=62
62 % 10 = 2
So 79-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C2H4ClNO/c3-1-2(4)5/h1H2,(H2,4,5)
79-07-2Relevant articles and documents
Vibrational spectra of chloroacetamide and three deuterated analogues in the crystalline state
Mido, Yoshiyuki,Yanagida, Akiyo,Garcia, M. Victoria
, p. 1751 - 1758 (1993)
The IR and Raman Spectra of α-chloroacetamide CH2ClCONH2 and three deuterated analogues CH2ClCOND2, CD2ClCONH2 and CD2ClCOND2, in the crystalline state have been studied.A complete interpretation of the spectra has been worked out on the basis of spectral comparison and of the normal coordinate analysis of the four analogues.
Amide bond formation in aqueous solution: Direct coupling of metal carboxylate salts with ammonium salts at room temperature
Nielsen, John,Tung, Truong Thanh
supporting information, p. 10073 - 10080 (2021/12/10)
Herein, we report a green, expeditious, and practically simple protocol for direct coupling of carboxylate salts and ammonium salts under ACN/H2O conditions at room temperature without the addition of tertiary amine bases. The water-soluble coupling reagent EDC·HCl is a key component in the reaction. The reaction runs smoothly with unsubstituted/substituted ammonium salts and provides a clean product without column chromatography. Our reaction tolerates both carboxylate (which are unstable in other forms) and amine salts (which are unstable/volatile when present in free form). We believe that the reported method could be used as an alternative and suitable method at the laboratory and industrial scales. This journal is
Effective Synthesis of 3,4-Diaryl-isoxazole-5-carboxamides and their Antiproliferative Properties
Maksimenko, Anna S.,Kislyi, Victor P.,Chernysheva, Natalia B.,Strelenko, Yuri A.,Zubavichus, Yan V.,Khrustalev, Victor N.,Semenova, Marina N.,Semenov, Victor V.
, p. 4260 - 4270 (2019/07/12)
A simple scalable procedure for the synthesis of 3,4-diaryl-isoxazole-5-carboxamides 6 under mild conditions from readily available material was developed. The targeted compounds 6, structural analogues of heat shock protein inhibitors, were obtained by the rearrangement of intermediate 3,4-diaryl-5-carboxamido-isoxazoline N-oxides 5. In contrast to carboxamido-isoxazoline oxides 5, base-catalyzed recyclization of 3,4-diaryl-5-(ethoxycarbonyl)isoxazoline N-oxides 9c unexpectedly yielded 5-hydroxy-1,2-oxazin-6-ones 17c instead of ethyl 3,4-diaryl-isoxazole-5-carboxylates 10. Crystal and molecular structure of 4-(2,5-dimethoxy-3,4-methylenedioxyphenyl)-5-hydroxy-3-phenyl-6H-1,2-oxazin-6-one 17c was established by single-crystal X-ray diffraction study. In a phenotypic sea urchin embryo assay, carboxamide 6f showed moderate antimitotic antitubulin activity compared to 5-unsubstituted 3,4-diarylisoxazoles 15, which featured strong microtubule destabilizing effect.