摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2,3,5-三氯联苯 | 55720-44-0

中文名称
2,3,5-三氯联苯
中文别名
三氯联苯;2,3ˊ,5-三氯联苯
英文名称
2,3,5-trichlorobiphenyl
英文别名
PCB 23;2,3,5-trichloro-biphenyl;2,3,5-Trichlor-biphenyl;2,3,5-Trichlorbiphenyl;1,2,5-trichloro-3-phenylbenzene
2,3,5-三氯联苯化学式
CAS
55720-44-0
化学式
C12H7Cl3
mdl
——
分子量
257.547
InChiKey
GBUCDGDROYMOAN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    41°C
  • 沸点:
    334.36°C (rough estimate)
  • 密度:
    1.3510 (rough estimate)
  • 保留指数:
    1796

计算性质

  • 辛醇/水分配系数(LogP):
    5.8
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

ADMET

代谢
多氯联苯(PCBs)通过吸入、口服和皮肤接触途径被吸收。它们通过血液运输,通常与白蛋白结合。由于它们的亲脂性特性,它们倾向于在富含脂质的组织中积累,如肝脏、脂肪组织和皮肤。多氯联苯的代谢非常缓慢,并且根据氯化的程度和位置而有所不同。多氯联苯通过微粒体单加氧酶系统代谢,该系统由细胞色素P-450酶催化,转化为极性代谢物,这些代谢物可以与谷胱甘肽和葡萄糖醛酸结合。主要的代谢物是羟基化产物,通过胆汁和粪便排出。多氯联苯的缓慢代谢意味着它们倾向于在身体组织中积累。(L4, T6)
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)
来源:Toxin and Toxin Target Database (T3DB)
毒理性
  • 毒性总结
PCB的作用机制因具体类型而异。类似于二噁烷的PCB会与芳基烃受体结合,通过改变基因的转录来扰乱细胞功能,主要是通过诱导肝脏第一阶段和第二阶段酶的表达,特别是细胞色素P450家族。人们认为PCB的大多数毒性效应是Ah受体结合的结果。其他PCB被认为会干扰钙通道和/或改变大脑中的多巴胺水平。PCB还通过改变甲状腺激素的生成和与雌激素受体结合来引起内分泌紊乱,这可能会刺激某些癌细胞的生长并产生其他类雌激素效应,如生殖功能障碍。它们还会通过结合如uteroglobin等受体蛋白而生物累积。(A3, A4, A30, A66)
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)
来源:Toxin and Toxin Target Database (T3DB)
毒理性
  • 致癌物分类
1, 对人类致癌。
1, carcinogenic to humans. (L135)
来源:Toxin and Toxin Target Database (T3DB)
毒理性
  • 健康影响
多氯联苯最常见的健康影响是皮肤状况,如氯痤疮和皮疹。长期暴露于多氯联苯还会导致肝脏、胃和肾脏损伤、黄疸、水肿、贫血、免疫系统变化、行为改变以及生殖能力受损。
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)
来源:Toxin and Toxin Target Database (T3DB)
毒理性
  • 暴露途径
口服(L4级);吸入(L4级);皮肤给药(L4级)
Oral (L4) ; inhalation (L4) ; dermal (L4)
来源:Toxin and Toxin Target Database (T3DB)
毒理性
  • 症状
慢性PCB暴露会导致如下症状:腹痛、恶心、呕吐、腹泻、头痛、眩晕、抑郁、紧张、皮肤和眼睛损伤、疲劳、月经周期不规律以及免疫力下降。
Chronic 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)
来源:Toxin and Toxin Target Database (T3DB)

SDS

SDS:79778b01895d17000ddf0f81c20f3089
查看

制备方法与用途

制备方法:

  • 用于农药残留量分析的标准。

用途简介:

  • 目前暂无具体内容。

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Willams William A., Environ. Sci. and Technol., 28 (1994) N 4, S 630-635
    摘要:
    DOI:
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 氯仿 作用下, 生成 2,3,5-三氯联苯
    参考文献:
    名称:
    Hinkel; Hey, Journal of the Chemical Society, 1928, p. 2787,2789
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Synthesis of Chlorinated Biphenyls by Suzuki Cross-Coupling Using Diamine or Diimine-Palladium Complexes
    作者:Tuula Kylmälä、Noora Kuuloja、Youjun Xu、Kari Rissanen、Robert Franzén
    DOI:10.1002/ejoc.200800119
    日期:2008.8
    and their reduced diamine counterparts 3b,3d–3g and 3i form complexes 4a–4i, 5b,5d–5g, and 5i with PdCl2 in DMF or methanol. Using 1 mol-% of the isolated complexes 4e and 5f many polychlorinated biphenyls (PCBs) can be prepared in moderate to excellent yields according to the Suzuki crosscoupling protocol with contact to air. Several 4-acetylbiphen
    几种新型二亚胺(Salen 型配体)2a-2i 及其还原的二胺对应物 3b、3d-3g 和 3i 在 DMF 或甲醇中与 PdCl2 形成复合物 4a-4i、5b、5d-5g 和 5i。根据与空气接触的铃木交叉偶联方案,使用 1 mol% 的分离配合物 4e 和 5f,可以以中等至极好的产率制备许多多氯联苯 (PCB)。几种4-乙酰联苯
  • Photoreactions of Polyhalobenzenes in Benzene. Formation of Terphenyls
    作者:Masahiro Nakada、Chihiro Miura、Hideaki Nishiyama、Futoshi Higashi、Toru Mori、Minoru Hirota、Tetsuo Ishii
    DOI:10.1246/bcsj.62.3122
    日期:1989.10
    Polychlorobenzenes, polybromobenzenes, and polychloropolybromobenzenes (C6H6−nXn) were photolyzed in benzene solutions; the products were analyzed by the GC/MS method. Both dehalogenation and phenylation were shown to take place competitively, producing (poly)halobenzenes bearing one less halogen atom (C6H7−nXn−1) and (poly)halobiphenyls (C6H6−nXn−1–C6H5) as the major products. Besides these products
    多氯苯、多溴苯和多氯多溴苯(C6H6−nXn)在苯溶液中光解;产物采用 GC/MS 方法分析。脱卤和苯基化都显示出竞争性,产生少一个卤素原子的(多)卤代苯(C6H7-nXn-1)和(多)卤代联苯(C6H6-nXn-1-C6H5)作为主要产品。除了这些产品之外,三联苯是通过形成的卤代联苯的连续苯基化产生的。只有当通过 2-氯联苯的途径成为可能时,多氯苯才会形成相应的三联苯;然而,多溴苯可以通过中间形成的任何异构溴联苯产生三联苯。还显示通过氯原子的间迁移发生异构化的程度要小得多。
  • Instruments for detecting low-molecular weight substance
    申请人:Mizukami Haruki
    公开号:US20050148097A1
    公开(公告)日:2005-07-07
    To provide the following instruments 1 and 2 as a low-molecular-weight substance detection instrument employing immunochromatography capable of detecting conveniently and sensitively detecting a low-molecular weight substance such as an environmental pollutant (e.g., a dioxin), as a target substance contained in a test sample: 1. an instrument, which comprises 1) a test sample application section with which a test sample is brought into contact; 2) a label product reaction section containing a label product containing, as a portion thereof, an antibody capable of binding to a target substance contained in the test sample, the label product being not bound to the reaction section; 3) an unbound label product capturing section containing an element capable of capturing the label product which is not bound to the target substance, the element being bound to the capturing section; and 4) a detection section containing a detection element which, when coming into contact with the target substance bound to the label product, causes a visually observable change, and 2. an instrument wherein a test sample is reacted with a labeled antibody containing, as a portion thereof, an antibody capable of binding to a target substance contained in the test sample, and the resultant reaction product is employed for detecting the target substance contained in the test sample.
    提供以下仪器1和2作为低分子量物质检测仪器,采用免疫层析技术,能够方便敏感地检测低分子量物质,例如环境污染物(例如二恶英),作为测试样品中包含的目标物质:1. 仪器,包括1)测试样品应用部分,用于将测试样品接触;2)标签产物反应部分,包含一种标签产物,其中包含一种能够结合到测试样品中的目标物质的抗体,标签产物未结合到反应部分;3)未结合标签产物捕获部分,包含一种能够捕获未结合到目标物质的标签产物的元素,该元素与捕获部分结合;以及4)检测部分,包含一种检测元素,当与结合到标签产物的目标物质接触时,会引起可视的变化;2. 仪器,其中测试样品与标记抗体反应,其中一部分包含能够结合到测试样品中的目标物质的抗体,产生的反应产物用于检测测试样品中包含的目标物质。
  • INSTRUMENTS FOR DETECTING LOW-MOLECULAR WEIGHT SUBSTANCE
    申请人:Enbiotec Laboratories Co., Ltd.
    公开号:EP1489420A1
    公开(公告)日:2004-12-22
    To provide the following instruments 1 and 2 as a low-molecular-weight substance detection instrument employing immunochromatography capable of detecting conveniently and sensitively detecting a low-molecular weight substance such as an environmental pollutant (e.g., a dioxin), as a target substance contained in a test sample: 1. an instrument, which comprises 1) a test sample application section with which a test sample is brought into contact; 2) a label product reaction section containing a label product containing, as a portion thereof, an antibody capable of binding to a target substance contained in the test sample, the label product being not bound to the reaction section; 3) an unbound label product capturing section containing an element capable of capturing the label product which is not bound to the target substance, the element being bound to the capturing section; and 4) a detection section containing a detection element which, when coming into contact with the target substance bound to the label product, causes a visually observable change, and 2. an instrument wherein a test sample is reacted with a labeled antibody containing, as a portion thereof, an antibody capable of binding to a target substance contained in the test sample, and the resultant reaction product is employed for detecting the target substance contained in the test sample.
    提供以下仪器 1 和 2,作为一种采用免疫层析技术的低分子量物质检测仪器,能够方便、灵敏地检测作为检测样品中目标物质的低分子量物质,如环境污染物(如二恶英): 1.仪器,包括:1)测试样品应用部分,测试样品与之接触;2)标签产品反应部分,包含标签产品,作为其一部分,该标签产品含有能够与测试样品中所含目标物质结合的抗体,标签产品未与反应部分结合;3) 非结合标签产品捕获部分,包含能够捕获未与目标物质结合的标签产品的元件,该元件与捕获部分结合;以及 4) 检测部分,包含检测元件,该元件与结合在标签产品上的目标物质接触时,会引起视觉上可观察到的变化,以及 2. 2. 一种仪器,其中测试样品与标记抗体反应,标记抗体的一部分能够与测试样品中的目标物质结合,反应产物用于检测测试样品中的目标物质。
  • Process for producing biaryl compound
    申请人:Hagiya Koji
    公开号:US20050096471A1
    公开(公告)日:2005-05-05
    A process for producing a biaryl compound, characterized by reacting an arylhydrazine compound, hydrogen peroxide and an aryl compound. When the reaction is conducted in the presence of a given metal or a compound of the metal or in the presence of a metal oxide obtained by reacting the given metal or a compound of the metal with hydrogen peroxide, then the yield of the biaryl compound is improved.
    一种生产双芳基化合物的工艺,其特征在于使芳基肼化合物、过氧化氢和芳基化合物反应。当反应是在某种金属或金属化合物存在下进行,或在某种金属或金属化合物与过氧化氢反应得到的金属氧化物存在下进行时,双芳基化合物的产率会提高。
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐