蒸汽密度
>6 (vs air)
质量水平
蒸汽压
1 mmHg ( 40 °C)
检测方案
≥99%
形式
solid or liquid
自燃温度
1060 °F
expl. lim.
6.6 %, 150 °F
技术
HPLC: suitable
UV/Vis spectroscopy: suitable
杂质
<0.020% water
折射率
n20/D 1.571 (lit.)
bp
214 °C (lit.)
mp
16 °C (lit.)
溶解性
water: insoluble
密度
1.454 g/mL at 25 °C (lit.)
λ
H2O reference
紫外吸收
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
应用
food and beverages
SMILES字符串
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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应用
- 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).
警示用语：
Warning
危险声明
危险分类
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2
WGK
WGK 3
闪点(°F)
235.4 °F
闪点(°C)
113.0 °C
法规信息
危险化学品
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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