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2043-43-8

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2043-43-8 Usage

General Description

Lactamide is a chemical compound that belongs to the amide group and is derived from lactic acid. It is a white, crystalline solid that is freely soluble in water and is used in a variety of industrial applications. Lactamide is used as a lubricant and release agent in the production of plastics and rubber, as well as in the production of pharmaceuticals, personal care products, and food additives. It is known for its ability to reduce friction and provide a smooth, non-sticky surface. Lactamide is also used as a surfactant, emulsifier, and corrosion inhibitor in various industrial processes. In addition to its industrial uses, lactamide is also being investigated for potential medical and pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2043-43-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,4 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2043-43:
(6*2)+(5*0)+(4*4)+(3*3)+(2*4)+(1*3)=48
48 % 10 = 8
So 2043-43-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H7NO2/c1-2(5)3(4)6/h2,5H,1H3,(H2,4,6)/t2-/m0/s1

2043-43-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name lactamide

1.2 Other means of identification

Product number -
Other names LACTAMIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2043-43-8 SDS

2043-43-8Relevant articles and documents

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Oeda

, p. 385,387 (1936)

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Highly Efficient Synthesis of Amino Acids by Amination of Bio-Derived Hydroxy Acids with Ammonia over Ru Supported on N-Doped Carbon Nanotubes

Xie, Zhenbing,Chen, Bingfeng,Peng, Fangfang,Liu, Mingyang,Liu, Huizhen,Yang, Guanying,Han, Buxing

, p. 5683 - 5689 (2020/09/21)

The amino acids have extensive applications, and their productions from biomass-derived feedstocks are very attractive. In this work, the synthesis of amino acids by amination of bio-derived hydroxy acids with ammonia over different metallic nano-catalysts supported on various supports is studied. It is found that Ru nano-catalysts on the nitrogen-doped carbon nanotubes (Ru/N?CNTs) have an outstanding performance for the reaction. Different hydroxy acids can be catalytically converted into the corresponding amino acids with yields up to 70.0 % under mild conditions, which is higher than those reported. The reasons for the high efficiency of the catalyst are investigated, and the reaction pathway is proposed on the basis of control experiments.

Promotion of catalytic properties of vanillin loaded MCM-41 by Cu(I) and Cu(II) for enhanced removal of quinoline contaminants

Arjmand, Mehdi,Fazaeli, Reza,Ghorbani, Mohammad Hossein,Kamani, Mina

, p. 4833 - 4841 (2020/09/16)

In the present study, to enhance removal of quinoline contaminants using natural active component, vanillin was loaded onto the MCM-41 (Mobile Component Material) nanoparticles in a simple way. The product was divided into two parts, which were improved by Copper(I) and Copper(II) salts. Promoted synthetic nanocatalysts (Cu(I)/Van./MCM-41, and Cu(II)/Van./MCM-41) were characterized using X-Ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Energy-Dispersive X-Ray Spectroscopy (EDS), Mapping, Fourier-Transform Infrared Spectroscopy (FTIR), and BET/BJH (Brunauer-Emmett-Teller (BET) and Barret-Joyner-Halenda (BJH)) techniques. To reach optimal conditions, experimental design was performed using Response Surface Methodology (RSM). The experiments were done with the aid of nanocomposites, in presence of ultraviolet radiation without any auxiliary oxidants. Degradation percentages were measured by an Ultraviolet (UV) spectrophotometer. The products were identified using Gas Chromatography–Mass (GC-Mass) technique, and some mechanisms for quinoline removal were proposed. The results indicated that Cu (I) showed better performance in enhanced removal of quinoline than Cu(II).

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