2,2-二氯丙酸

2,2-二氯丙酸结构式
2,2-二氯丙酸结构式
品牌特惠专场
常用名 2,2-二氯丙酸 英文名 2,2-Dichloropropionic acid
CAS号 75-99-0 分子量 142.96900
密度 1.4014 沸点 202°C
分子式 C3H4Cl2O2 熔点 166°C (dec.)
MSDS 中文版 美版 闪点 >110°C
符号 GHS02 GHS07
GHS02, GHS07
信号词 Danger

Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors.

J. Med. Chem. 51 , 6740-51, (2008)

The work provides a new model for the prediction of the MAO-A and -B inhibitor activity by the use of combined complex networks and QSAR methodologies. On the basis of the obtained model, we prepared and assayed 33 coumarin derivatives, and the theoretical pr...

Quantitative nuclear magnetic resonance (QNMR) spectroscopy for assessing the purity of technical grade agrochemicals: 2,4-dichlorophenoxyacetic acid (2,4-D) and sodium 2,2-dichloropropionate (Dalapon sodium).

J. Agric. Food Chem. 50(12) , 3366-74, (2002)

Comparison of quantitative NMR spectroscopy (QNMR) with chromatographic methods such as gas chromatography (GC) or high-pressure liquid chromatography (HPLC) for the determination of the purity of and impurities in technical grade agrochemicals, 2,4-dichlorop...

Effects of water management and herbicide treatments on red rice control.

Meded. Rijksuniv. Gent. Fak. Landbouwkd. Toegep. Biol. Wet. 67(3) , 441-9, (2002)

Two field experiments were conducted in 1999 and 2000 at Zeme (Pavia, Italy) to determine the effects of water managements and herbicide treatments on red rice control. In the first experiment, all plots were flooded 10-13 cm deep from April 1 to May 17 in 19...

Analyzing haloacetic acids using gas chromatography/mass spectrometry.

Water Res. 35(6) , 1599-602, (2001)

Haloacetic acids (HAAs) are a group of disinfection by-products formed in chlorinated water. Due to their potential health effects and widespread occurrences, HAAs are regulated in drinking water in the United States under a promulgated regulation. To better ...

Diversity of alpha-halocarboxylic acid dehalogenases in bacteria isolated from a pristine soil after enrichment and selection on the herbicide 2,2-dichloropropionic acid (Dalapon).

Environ. Microbiol. 5(1) , 48-54, (2003)

Five pure cultures of bacteria (strains DA1-5) able to degrade 2,2-dichloropropionic acid (22DCPA) were isolated for the first time from pristine bulk soil samples. From 16S rDNA analysis, it was concluded that strains DA2, DA3 and DA4 were members of the Bra...

Degradation of aliphatic halogen-substituted pesticides by dehalogenase isolated from Pseudomonas alcaligenes. Identification and properties of the enzyme.

Sci. Total Environ. 123-124 , 267-77, (1992)

Some characteristics of a 2,2-dichloropropionate dehalogenase induced in a bacterial strain capable of degrading high concentrations of the herbicide dalapon were studied. Polyacrilamide gel electrophoresis of the crude cell free extracts identified only one ...

[The tolerance and residue accumulation of sodium-2,2-dichloropropionate (Dalapon) administered over 90 days to dairy cows].

DTW Dtsch. Tierarztl. Wochenschr. 99(4) , 148-51, (1992)

The influence of the pesticide Sodium-2,2-dichlorpropionate (Na-DCP; Dalapon) was investigated on dairy cows concerning of its effect on ability and health condition. The investigations were carried out in practice using several parameters (feeding, efficienc...

The occurrence of the herbicide dalapon (2,2-dichloropropionate) in potable water as a disinfection by-product.

J. Environ. Monit. 13(2) , 252-6, (2011)

Salts of 2,2-dichloropropionic acid, such as dalapon, are well known as herbicides and are regulated as such in potable water in Australia and elsewhere. It is also an identified disinfection by-product (DBP), but little is known about the compound's formatio...

Sublethal effects of 2,2-dichloropropionic acid (dalapon) on Fossaria cubensis, intermediate host of the liver fluke, Fasciola hepatica.

Bull. Environ. Contam. Toxicol. 45(3) , 343-9, (1990)

Effects of glyphosate and dalapon on total free amino acid profiles of Pseudosuccinea columella snails.

Bull. Environ. Contam. Toxicol. 64(2) , 258-62, (2000)