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2,3,4-Trichlorobiphenyl

HCID 41541
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
25323-68-6
Standard SMILES
Clc1ccc(-c2ccccc2)c(Cl)c1Cl
InChIKey
IUYHQGMDSZOPDZ-UHFFFAOYSA-N
Molecular formula
C12H7Cl3
Average molar mass
257.5 g/mol
Monoisotopic mass
255.961333

Overview

2,3,4-trichlorobiphenyl is a trichlorobiphenyl that is biphenyl in which the hydrogens at positions 2, 3, and 4 on one of the benzene rings are replaced by chlorines. It is a trichlorobenzene and a trichlorobiphenyl.

Names & identifiers

Preferred name
2,3,4-Trichlorobiphenyl
IUPAC
1,2,3-trichloro-4-phenylbenzene
English name
2,3,4-TRICHLOROBIPHENYL
Molecular formula
C12H7Cl3
Molecular weight
257.54

Names & synonyms

2,3,4-Trichlorobiphenyl55702-46-02,3,4-TRICHLORO-1,1'-BIPHENYLPCB 211,1'-Biphenyl, 2,3,4-trichloro-UNII-61NYE2032D61NYE2032DDTXSID0074180CHEBI:34222RefChem:53570DTXCID3041950TRICHLOROBIPHENYL
Show more names
BZNO 212,3,4-CBPCB NO 212,3,4-Trichlorobiphenyl-d5PCB No. 21 10 μg/mL in IsooctanePCB NO.21-2,3,4-Trichlorobiphenyl234TRICHLOROBIPHENYL(2,3,4-TRICHLOROISOMER)
25323-68-61,2,3-trichloro-4-phenylbenzenePCB No. 21TrichlorodiphenylBiphenyl, trichloro-Apirolio 1431 CPyranol 1499Trichloro-1,1'-biphenyl

Database identifiers

CAS
25323-68-6、55702-46-0
PubChem CID
41541
DTXSID
DTXSID0074180
ChEBI
CHEBI:34222
UNII
61NYE2032D
EC Number
690-243-4

Properties

Computed structural properties

XLogP
5.9
Topological polar surface area
0 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
0
Rotatable bonds
1
Heavy atoms
15
Formal charge
0
Complexity
201

Experimental & physicochemical properties

SpringerMaterials Properties13C nuclear magnetic resonance spectrum
LogP5.68
Endocrine DisruptorsPotential endocrine disrupting compound

Physicochemical properties

Melting point
102 °C · 102°C
Boiling point
334.36 °C · 334.36°C (rough estimate)
Density
1.351 · 1.3510 (rough estimate)
refractive index
1.604 · 1.6040 (rough estimate)
Henry's Law Constant
4.3 · 4.3×10-3 mol/(m3Pa) at 25℃, Paasivirta and Sinkkonen (2009)
CAS DataBase Reference
55702 · 55702-46-0
FDA UNII
61 NYE2032D · 61NYE2032D
EPA Substance Registry System
2 · 2,3,4-Trichlorobiphenyl (55702-46-0)

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 3 items

This chemical does not meet GHS hazard criteria for 100% (3 of 3) of all reports.

Not Classified

Aggregated GHS information provided per 3 reports by companies from 1 notifications to the ECHA C&L Inventory.

Hazard information

Hazard Classes and CategoriesNot Classified

Safety & protection

Minimum Risk LevelIntermediate Oral: 0.03 ug/kg/day (L134)

Toxicology

Treatment · 1 item

There are no specific treatments for PCB poisoning, since it is not usually recognized until after substantial chronic exposure. Only preventing further exposure and treating the observed symptoms can be done. Acute inhalation can be treated by administering oxygen. (L4)

Health Effects · 1 item

The most common health effects of PCBs are skin conditions such as chloracne and rashes. Chronic PCB exposure has also been shown to cause liver, stomach and kidney, damage, jaundice, edema, anemia, changes in the immune system, behavioral alterations, and impaired reproduction. (L4)

Exposure RoutesOral (L4) ; inhalation (L4) ; dermal (L4)
Toxicity Summary · 1 item

The mechanism of action varies with the specific PCB. Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. Most of the toxic effects of PCBs are believed to be results of Ah receptor binding. Other PBCs are believed to interfere with calcium channels and/or change brain dopamine levels. PCBs can also cause endocrine disurption by altering the production of thyroid hormones and binding to estrogen receptors, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. They will bioaccumulate by binding to receptor proteins such as uteroglobin. (A3, A4, A30, A66)

Chemistry & industry

Pharmacology

Metabolism/Metabolites · 1 item

PCBs are absorbed via inhalation, oral, and dermal routes of exposure. They are trasported in the blood, often bound to albumin. Due to their lipophilic nature they tend to accumulate in lipid-rich tissues, such as the liver, adipose, and skin. Metabolism of PCBs is very slow and varies based on the degree and position of chlorination. PCBs are metabolized by the microsomal monooxygenase system catalyzed by cytochrome P-450 enzymes to polar metabolites that can undergo conjugation with glutathione and glucuronic acid. The major metabolites are hydroxylated products which are excreted in the bile and faeces. The slow metabolism of PCBs means they tend to accumulate in body tissues. (L4, T6)

Uses & manufacturing

Uses · 1 item

PCBs were used as coolants and lubricants in transformers, capacitors, and other electrical devices (such as fluorescent lights and refridgerators) produced before 1977. PCBs may contaminate the air and water near hazardous waste sites. In addition, PCBs bioaccumulate in the environment and may be found in fish, meat, and dairy products. (L4)

Applications

Uses2,3,4-Trichlorobiphenyl is a polychlorinated biphenyl (PCB) congeners.

Upstream & downstream products

Downstream products

3,4-Dichlorobiphenyl

Additional notes

DefinitionChEBI: A trichlorobiphenyl that is biphenyl in which the hydrogens at positions 2, 3, and 4 on one of the benzene rings are replaced by chlorines.

Related reactions

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Nikkaji
J150.405C
Signs and SymptomsChronic PCB exposure results in symptoms such as abdominal pain, nausea, vomiting, diarrhea, headache, dizziness, depression, nervousness, dermal and ocular lesions, fatigue, irregular menstrual cycles and a lowered immune response. (A3)
Carcinogen Classification1, carcinogenic to humans. (L135)
Toxicity DataLD50: 1010 mg/kg (Oral, Rat) (T14) LD50: 880 mg/kg (Intraperitoneal, Mouse) (T14)