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35487

Supelco

4,4′-DDE

PESTANAL®, analytical standard

别名:

1,1-二氯-2,2-双(4-氯苯基)乙烯, 4,4′-DDE

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25 G
¥234.05
100 G
¥384.49
500 G
¥1,569.17

¥234.05

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25 G
¥234.05
100 G
¥384.49
500 G
¥1,569.17

About This Item

线性分子式:
(ClC6H4)2C=CCl2
CAS Number:
72-55-9
分子量:
318.03
Beilstein:
1913355
EC 号:
200-784-6
MDL编号:
MFCD00000837
UNSPSC代码:
41116107
PubChem化学物质编号:
329755172
NACRES:
NA.24

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等级

analytical standard

质量水平

100

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

mp

88-90 °C (lit.)

应用

agriculture
environmental

包装形式

neat

SMILES字符串

Clc1ccc(cc1)\C(=C(/Cl)Cl)c2ccc(Cl)cc2

InChI

1S/C14H8Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8H

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此商品
F3606653586F3401
4-氟苯胺 99%

F3800

4-氟苯胺

3-氟苯胺 99%

F3606

3-氟苯胺

4-氟-1,2-苯二胺 97%

653586

4-氟-1,2-苯二胺

2-氟苯胺 ≥99%

F3401

2-氟苯胺

assay

99%

assay

99%

assay

97%

assay

≥99%

form

liquid

form

liquid

form

-

form

-

density

1.173 g/mL at 25 °C (lit.)

density

1.156 g/mL at 25 °C (lit.)

density

-

density

1.151 g/mL at 25 °C (lit.)

bp

187 °C/767 mmHg (lit.)

bp

186 °C/756 mmHg (lit.)

bp

-

bp

182-183 °C (lit.)

refractive index

n20/D 1.539 (lit.)

refractive index

n20/D 1.542 (lit.)

refractive index

-

refractive index

n20/D 1.544 (lit.)

一般描述

在有氧环境中，可以发现4，4′-DDE是三氯-2，2-双（4-氯苯基）乙烷[1]的分解产物。[2]它可以像典型的强效雄激素受体拮抗剂一样起作用。[2]

应用

有关合适的仪器技术的更多信息，请参阅产品′的检验报告。想要获得更多支持，请联系技术服务部。

法律信息

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

警示用语：

Danger

危险分类

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - STOT RE 1 Oral

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

危险化学品
  • 技术规格说明书

    • 历史批次信息供参考:

    分析证书(COA)

    Lot/Batch Number
    BCCH4254
    BCCB7683
    BCBS5816V

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    C V Eadsforth et al.
    Xenobiotica; the fate of foreign compounds in biological systems, 16(6), 555-566 (1986-06-01)
    o-Fluoroaniline is rapidly metabolized and excreted in rats, rabbits and marmosets. Following a single oral dose of 14C-fluoroaniline of about 20 mg/kg, more than 80% of the dose is excreted in 0-24 h, the urine being the major route of
    Meizhen Wang et al.
    Environmental science and pollution research international, 20(9), 6201-6209 (2013-04-17)
    To develop a bacterial bioaugmentation system for fluorine-containing industrial wastewater treatment, optimal conditions for 4-fluoroaniline (4-FA) degradation and autoinducer release in Acinetobacter sp. TW were determined. Quorum sensing in biofilms of strain TW was also investigated. Different optimal conditions exist
    G B Scarfe et al.
    Xenobiotica; the fate of foreign compounds in biological systems, 29(2), 205-216 (1999-04-13)
    1. The urinary metabolic fate of 4-fluoroaniline (4-FA) and 1-[13C]-4-fluoroacetanilide (4-FAA) has been studied using NMR-based methods after 50 and 100 mg kg(-1) i.p. doses respectively to the male Sprague-Dawley rat. 2. 4-FA was both ortho- and para-hydroxylated. The major
    I M Rietjens et al.
    Chemico-biological interactions, 77(3), 263-281 (1991-01-01)
    Metabolism and bioactivation of fluoroanilines was studied both in vitro in microsomal systems and in vivo. 4-Fluoroaniline and pentafluoroaniline and their non-para fluorinated analogues were used as the model compounds. Special attention was focussed on bioactivation to reactive benzoquinoneimines. Cytochrome
    J G Bundy et al.
    Xenobiotica; the fate of foreign compounds in biological systems, 32(6), 479-490 (2002-08-06)
    1. Little is known about metabolism of xenobiotics by earthworms, despite their importance in soil ecotoxicity testing. Normal earthworms and earthworms treated with antibiotics to ensure inhibition of gut microflora were exposed to two model xenobiotic compounds, 4-fluoroaniline and 4-fluorobiphenyl
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