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23320

Sigma-Aldrich

3-Chloroaniline

puriss., ≥99.0% (GC)

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About This Item

Linear Formula:
ClC6H4NH2
CAS Number:
108-42-9
Molecular Weight:
127.57
Beilstein:
605969
EC Number:
203-581-0
MDL number:
MFCD00007765
UNSPSC Code:
12352100
PubChem Substance ID:
329752411

vapor pressure

1 mmHg ( 63.5 °C)

grade

puriss.

Assay

≥99.0% (GC)

refractive index

n20/D 1.594 (lit.)
n20/D 1.594

bp

95-96 °C/11 mmHg (lit.)

mp

−11-−9 °C (lit.)

density

1.206 g/mL at 25 °C (lit.)

SMILES string

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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Other Notes

This product has been replaced by C22407-ALDRICH | 3-Chloroaniline 99%

Signal Word

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
1254002
044315/1
040547/1
034173/1
011480/1

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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
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
N Boon et al.
Applied and environmental microbiology, 66(7), 2906-2913 (2000-07-06)
A strain identified as Comamonas testosteroni I2 was isolated from activated sludge and found to be able to mineralize 3-chloroaniline (3-CA). During the mineralization, a yellow intermediate accumulated temporarily, due to the distal meta-cleavage of chlorocatechol. This strain was tested
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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