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Merck
CN

C22407

3-氯苯胺

99%

别名:

1-氨基-3-氯苯, 3-氨基-1-氯苯, 3-氯-1-氨基苯, 3-氯苯胺, 5-氯苯胺, 间氨基氯苯, 间氯苯胺

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关于此项目

线性分子式:
ClC6H4NH2
化学文摘社编号:
分子量:
127.57
Beilstein:
605969
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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蒸汽压

1 mmHg ( 63.5 °C)

方案

99%

表单

liquid

折射率

n20/D 1.594 (lit.)

沸点

95-96 °C/11 mmHg (lit.)

mp

−11-−9 °C (lit.)

密度

1.206 g/mL at 25 °C (lit.)

SMILES字符串

Nc1cccc(Cl)c1

InChI

1S/C6H6ClN/c7-5-2-1-3-6(8)4-5/h1-4H,8H2

InChI key

PNPCRKVUWYDDST-UHFFFAOYSA-N

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应用

  • 睾酮单胞菌第二信使c-二- gmp水平的升高促进了3-氯苯胺生物膜的形成和基于生物膜的生物降解。:该研究表明,睾酮单胞菌中c-二gmp水平的增加可以促进生物膜的形成和3-氯苯胺的生物降解效率,这表明了改善生物修复过程的策略(Wu et al., 2015)。
  • 恶臭假单胞菌T57甲苯双加氧酶降解氯苯胺的研究:该研究调查了恶臭假单胞菌T57的甲苯双加氧酶在降解氯苯胺中的作用,为酶的机制和处理氯苯胺污染物的潜在应用提供了见解(Nitisakulkan et al., 2014)。
  • 生物增强作为保护活性污泥微生物群落的结构和功能免受3-氯苯胺冲击负荷的工具:该研究评估了生物增强在维持暴露于3-氯苯胺的活性污泥系统中微生物群落的稳定性和功能方面的有效性,支持其在废水处理中的应用(Boon et al., 2003)。

警示用语:

Danger

危险分类

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Sens. 1B - STOT RE 2 Oral

靶器官

Endocrine system

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 2

闪点(°F)

244.4 °F - closed cup

闪点(°C)

118 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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W Swenson et al.
Environmental microbiology, 2(5), 564-571 (2001-03-10)
We present a method for selecting entire microbial ecosystems for bioremediation and other practical purposes. A population of ecosystems is established in the laboratory, each ecosystem is measured for a desired property (in our case, degradation of the environmental pollutant
J Alary et al.
Toxicology, 59(2), 211-223 (1989-12-01)
In order to investigate the various steps of chlorpropham (CIPC) metabolism which could be influenced by cadmium, isolated rat hepatocytes were incubated in the presence of CIPC (0.1 mM) and of increasing Cd concentrations (0-180 microM). The results showed that
G O Rankin et al.
Toxicology, 38(3), 269-283 (1986-03-01)
Aniline (A) and its monochlorophenyl derivatives (2-CA, 3-CA and 4-CA) are widely-used chemical intermediates. In the present study, the in vivo and in vitro nephrotoxic potential of these compounds was assessed in Fischer 344 rats. In the in vivo experiments
Michael W Falk et al.
Water research, 44(17), 5109-5115 (2010-09-25)
The effects of toxins at ambient concentrations on microbial activity and community dynamics are poorly understood. We operated 4 membrane bioreactors (MBRs) in parallel; two reactors were continuously exposed to the toxin 3-chloroaniline (3-CA) at environmentally relevant levels, representing 25%
N Boon et al.
Applied and environmental microbiology, 67(3), 1107-1115 (2001-03-07)
We examined the diversity of the plasmids and of the gene tdnQ, involved in the oxidative deamination of aniline, in five bacterial strains that are able to metabolize both aniline and 3-chloroaniline (3-CA). Three strains have been described and identified

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