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Merck

C22407

3-Chloroaniline

99%

Sinónimos:

1-Amino-3-chlorobenzene, 3-Amino-1-chlorobenzene, 3-Chloro-1-aminobenzene, 3-Chlorobenzenamine, 3-Chlorophenylamine, 5-Chloroaniline, m-Aminochlorobenzene, m-Chloroaniline, m-Chlorophenylamine

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Fórmula lineal:
ClC6H4NH2
Número CAS:
108-42-9
Peso molecular:
127.57
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24892479
EC Number:
203-581-0
Beilstein/REAXYS Number:
605969
MDL number:
MFCD00007765
Assay:
99%
Form:
liquid

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InChI key

PNPCRKVUWYDDST-UHFFFAOYSA-N

InChI

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

SMILES string

Nc1cccc(Cl)c1

vapor pressure

1 mmHg ( 63.5 °C)

assay

99%

form

liquid

refractive index

n20/D 1.594 (lit.)

bp

95-96 °C/11 mmHg (lit.)

mp

−11-−9 °C (lit.)

density

1.206 g/mL at 25 °C (lit.)

Quality Level

200

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Categorías relacionadas

Application

  • Elevated level of the second messenger c-di-GMP in Comamonas testosteroni enhances biofilm formation and biofilm-based biodegradation of 3-chloroaniline.: This research reveals that increased levels of c-di-GMP in Comamonas testosteroni enhance both biofilm formation and the biodegradation efficiency of 3-chloroaniline, suggesting a strategy to improve bioremediation processes (Wu et al., 2015).
  • Degradation of chloroanilines by toluene dioxygenase from Pseudomonas putida T57.: The study investigates the role of toluene dioxygenase from Pseudomonas putida T57 in degrading chloroanilines, providing insights into the enzymatic mechanisms and potential applications in treating chloroaniline pollutants (Nitisakulkan et al., 2014).
  • Bioaugmentation as a tool to protect the structure and function of an activated-sludge microbial community against a 3-chloroaniline shock load.: The study evaluates the effectiveness of bioaugmentation in maintaining the stability and functionality of microbial communities in activated sludge systems exposed to 3-chloroaniline, supporting its application in wastewater treatment (Boon et al., 2003).

signalword

Danger

Hazard Classifications

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

target_organs

Endocrine system

Clase de almacenamiento

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

wgk

WGK 2

flash_point_f

244.4 °F - closed cup

flash_point_c

118 °C - closed cup

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
MKCW2621
MKCV4036
MKCQ6277
MKCQ1543
MKCM7626

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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
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
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%
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
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