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256412

Sigma-Aldrich

1,2,4-Trichlorobenzene

suitable for HPLC, ≥99%

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About This Item

Empirical Formula (Hill Notation):
C6H3Cl3
CAS Number:
120-82-1
Molecular Weight:
181.45
Beilstein:
956819
EC Number:
204-428-0
MDL number:
MFCD00000547
UNSPSC Code:
12190000
PubChem Substance ID:
329752809
NACRES:
NA.04

vapor density

>6 (vs air)

Quality Level

100

vapor pressure

1 mmHg ( 40 °C)

Assay

≥99%

form

solid or liquid

autoignition temp.

1060 °F

expl. lim.

6.6 %, 150 °F

technique(s)

HPLC: suitable
UV/Vis spectroscopy: suitable

impurities

<0.020% water

refractive index

n20/D 1.571 (lit.)

bp

214 °C (lit.)

mp

16 °C (lit.)

solubility

water: insoluble

density

1.454 g/mL at 25 °C (lit.)

λ

H2O reference

UV absorption

λ: 308 nm Amax: 1.00
λ: 310 nm Amax: 0.50
λ: 350 nm Amax: 0.05
λ: 375-400 nm Amax: 0.01

application(s)

food and beverages

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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Related Categories

Application


  • Application of electrospun polyacrylonitrile/Zn-MOF-74@GO nanocomposite as the sorbent for online micro solid-phase extraction of chlorobenzenes in water, soil, and food samples prior to liquid chromatography analysis: This article explores the use of an electrospun polyacrylonitrile/Zn-MOF-74@GO nanocomposite for the extraction of chlorobenzenes, including 1,2,4-Trichlorobenzene, from various samples. The method shows high efficiency and selectivity, making it suitable for environmental and food safety applications (Amini et al., 2021).

  • Facile synthesis and immobilization of functionalized covalent organic framework-1 for electrochromatographic separation: This research involves the synthesis and application of a functionalized covalent organic framework for the electrochromatographic separation of various compounds, including chlorobenzenes like 1,2,4-Trichlorobenzene. The method shows potential for analytical and separation sciences (Bao et al., 2021).

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Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H315,H410

Hazard Classifications

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

WGK

WGK 3

Flash Point(F)

235.4 °F

Flash Point(C)

113.0 °C

Regulatory Information

危险化学品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis and characterization of several Ni/NiAl2O4 catalysts active for the 1, 2, 4-trichlorobenzene hydrodechlorination.
Cesteros Y, et al.
Applied Catalysis. B, Environmental, 25(4), 213-227 (2000)
The effect of trichlorobenzene solvent geometry on the morphologies of C60 nano/microcrystals produced from solution.
Liu DD, et al.
Materials Research Bulletin, 73, 65-69 (2016)
Sorption and cosorption of 1, 2, 4-trichlorobenzene and tannic acid by organo-clays.
Dentel SK, et al.
Water Research, 32(12), 3689-3697 (1998)
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
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.
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