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2,4,6-トリクロロビフェニル

2,4,6-Trichlorobiphenyl

HCID 37247
ノート反応
基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
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基本情報

CAS
35693-92-6
標準SMILES
Clc1cc(Cl)c(-c2ccccc2)c(Cl)c1
InChIKey
MTLMVEWEYZFYTH-UHFFFAOYSA-N
分子式
C12H7Cl3
平均分子量
257.5 g/mol
単同位体質量
255.961333

概要

2,4,6-Trichlorobiphenyl is one of 209 polychlorinated biphenyls (PCBs). PCBs are a group of synthetic organic compounds with 1-10 chlorine atoms attached to biphenyl. They were manufactured as commercial mixtures but banned in the 1970's because they were found to bioaccumulate and cause harmful health effects. However, PCBs do not break down readily and are still found in the environment. (L4)

名称と識別子

優先名称
2,4,6-Trichlorobiphenyl
IUPAC
1,3,5-trichloro-2-phenylbenzene
現地名
2,4,6-トリクロロビフェニル
英語名
2,4,6-Trichlorobiphenyl
分子式
C12H7Cl3
分子量
257.54

名称と別名

2,4,6-TRICHLOROBIPHENYL35693-92-62,4,6-Trichloro-1,1'-biphenyl1,3,5-trichloro-2-phenylbenzene2,4,6-Tcb0BYA65Q6C2PCB 30DTXSID7073482RefChem:53579DTXCID9039076621-526-21,1'-Biphenyl, 2,4,6-trichloro-
名称をさらに表示
2,4,6-トリクロロ[1,1'-ビフェニル]2,4,6-トリクロロビフェニル2,4,6-トリクロロ-1,1'-ビフェニル2,4,6‐トリクロロビフェニル標準品2,4,6‐トリクロロビフェニル標準液2,4,6-TRICB (UNLABELED 35 UG/ML IN ISOOCTANE)2,4,6-トリクロロビフェニル (35ΜG/ML イソオクタン溶液)2,4,6-トリクロロビフェニル, 100 µg/mL in Isooctane2,4,6-トリクロロビフェニル標準液6-PCBBZ NO 302,4,6-PCBPCB NO 30PCB No.30PCB NoC20003000 PCB No. 30PCB No 30 solutionbiphenyl,2,4,6-trichloro-
PCB No. 30PCB No. 30 100 microg/mL in IsooctaneUNII-0BYA65Q6C2MTLMVEWEYZFYTH-UHFFFAOYSA-NMFCD001529002,4,6-TricbSCHEMBL2932603CHEMBL1797263

物性

構造計算による物性

XLogP
5.7
極性表面積
0 Ų
水素結合供与体数
0
水素結合受容体数
0
回転可能結合数
1
重原子数
15
形式電荷
0
複雑度
189

実験および物理化学的性質

SpringerMaterials Properties13C nuclear magnetic resonance spectrum
LogP5.47
Collision Cross Section149.6 Ų [M-Cl+O]-

物理化学的性質

融点
63 ℃ · 63℃
沸点
334.36 °C · 334.36°C (rough estimate)
比重(密度)
1.351 · 1.3510 (rough estimate)
屈折率
1.39 · n/D1.3900-1.3940
闪点
-4 °C · -4 °C
貯蔵温度
2 · 2-8°C
水溶解度
252.4 ug/L · 252.4ug/L(25℃)
Henry's Law Constant
1.5 · 1.5×10-2 mol/(m3Pa) at 25℃, Dunnivant et al. (1988)
EPAの化学物質情報
2 · 2,4,6-Trichlorobiphenyl (35693-92-6)

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

GHS分類

GHS Classification · 5 件

This chemical does not meet GHS hazard criteria for 7.1% (3 of 42) of reports.

Warning

H373 (92.9%): May causes damage to organs through prolonged or repeated exposure [Warning Specific target organ toxicity, repeated exposure]

P260, P273, P319, P391, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 42 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Regulatory InformationSubstance: 2,4,6-Trichlorobiphenyl
Hazard Classes and CategoriesSTOT RE 2 (92.9%)

安全と保護具

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

毒性情報

Treatment · 1 件

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 件

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 Routes

化学と産業

薬理情報

Metabolism/Metabolites · 1 件

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)

用途と製造

Uses · 1 件

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)

応用分野

使用2,4,6-Trichlorobiphenyl is a polychlorinated biphenyl (PCB) congeners.

上流・下流製品情報

下流製品

2,6-ジクロロ[1,1'-ビフェニル]

サプライヤー31 社

陕西缔都医药有限责任公司029-81124775 17791530730 · [email protected]
阿诺西(上海)生物技术有限公司400-1107768 15058188853 · [email protected]

関連反応

0 件
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現在のフィルター条件では反応記録がありません。

化合物ノート

読み込み中…

このページの内容基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート

データベース識別子

CAS
35693-92-6
PubChem CID
37247
DTXSID
DTXSID7073482
ChEMBL
CHEMBL1797263
UNII
0BYA65Q6C2
EC Number
621-526-2
Nikkaji
J150.407J
Oral (L4) ; inhalation (L4) ; dermal (L4)
Toxicity Summary · 1 件

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)

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)

安全データ

ridadr
2315
risk_code
11-38-50/53-65-67-33
化審法
-1
安衛法
特定化学物質障害予防規則:第1類物質,57,57-2
消防法
危-4-1-II
hazard_code
F,Xn,N
safety_code
60-61-62-16
hazard_class
9
packing_group
II
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