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48507

1,2,4-Trichlorobenzene

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C6H3Cl3
CAS Number:
120-82-1
Molecular Weight:
181.45
EC Number:
204-428-0
UNSPSC Code:
12352200
PubChem Substance ID:
24872019
Beilstein/REAXYS Number:
956819
MDL number:
MFCD00000547
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grade

analytical standard

vapor density

>6 (vs air)

vapor pressure

1 mmHg ( 40 °C)

autoignition temp.

1060 °F

expl. lim.

6.6 %, 150 °F

packaging

ampule of 5000 mg

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

refractive index

n20/D 1.571 (lit.)

bp

214 °C (lit.)

mp

16 °C (lit.)

density

1.454 g/mL at 25 °C (lit.)

application(s)

environmental

SMILES string

Clc1ccc(Cl)c(Cl)c1

InChI

1S/C6H3Cl3/c7-4-1-2-5(8)6(9)3-4/h1-3H

InChI key

PBKONEOXTCPAFI-UHFFFAOYSA-N

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pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113.0 °C - closed cup

ppe

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
LB88442V
LB84864V
LB62847
LB55216
LB53828

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Tatyana Balandina et al.
Chemical communications (Cambridge, England), 49(22), 2207-2209 (2013-02-12)
STM brings to light chirality aspects of the self-assembly of a functionalized helicene at the interface between a liquid and the solid substrates, gold and graphite. This reveals conditions for conglomerate formation.
Fredrick Orori Kengara et al.
The Science of the total environment, 408(16), 3359-3366 (2010-05-04)
A soil-borne microbial community isolated from a contaminated site was previously shown to mineralize 1,2,4-trichlorobenzene (1,2,4-TCB) under aerobic conditions. The key degrader in this community was identified as Bordetella sp. F2. The objective of the study was to test the
Ernest Marco-Urrea et al.
Bioresource technology, 100(23), 5757-5762 (2009-07-21)
Extracellular hydroxyl radical ((*)OH) production via quinone redox cycling in Trametes versicolor, grown in a chemically defined medium, was investigated to degrade trichloroethylene (TCE), perchloroethylene (PCE), 1,2,4- and 1,3,5-trichlorobenzene (TCB). The activity of the enzymes catalyzing the quinone redox cycle
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