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Merck
CN

36765

Supelco

2,6-二乙基苯胺

PESTANAL®, analytical standard

别名:

2-氨基-1,3-二乙基苯

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关于此项目

线性分子式:
(C2H5)2C6H3NH2
化学文摘社编号:
分子量:
149.23
Beilstein:
1423626
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
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等级

analytical standard

蒸汽压

0.02 mmHg ( 20 °C)

产品线

PESTANAL®

方案

98-100% (GC)

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.545 (lit.)

沸点

243 °C (lit.)

密度

0.906 g/mL at 25 °C (lit.)

应用

agriculture
environmental

包装形式

neat

SMILES字符串

CCc1cccc(CC)c1N

InChI

1S/C10H15N/c1-3-8-6-5-7-9(4-2)10(8)11/h5-7H,3-4,11H2,1-2H3

InChI key

FOYHNROGBXVLLX-UHFFFAOYSA-N

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应用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

法律信息

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

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

10 - Combustible liquids

WGK

WGK 2

闪点(°F)

239.0 °F - closed cup

闪点(°C)

115 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A D Kligerman et al.
Mutation research, 441(1), 95-101 (1999-05-04)
Alachlor is a widely used herbicide for which there is significant human exposure, principally through groundwater contamination and inhalation. Because alachlor is purported to be carcinogenic and mutagenic, we initiated studies to determine if induced cytogenetic damage could be used
Urinary biomonitoring for alachlor exposure in commercial pesticide applicators by immunoassay.
R E Biagini et al.
Bulletin of environmental contamination and toxicology, 54(2), 245-250 (1995-02-01)
S J Logusch et al.
Journal of agricultural and food chemistry, 47(5), 2125-2129 (1999-12-20)
Rat liver tissue homogenates were utilized for in vitro enzymatic conversion of 2,6-diethylaniline (DEA) to the important alachlor metabolite 4-amino-3,5-diethylphenyl sulfate (ADEPS), which was also generated as a radiolabeled standard for use in metabolism studies. ADEPS formation in rodents is
Q Li et al.
Mutation research, 395(2-3), 151-157 (1998-02-18)
N,N-Diethylaniline is a reagent used in organic synthesis and is an important intermediate in the manufacturing of dyes. To evaluate its genotoxicity, we examined whether it can induce sister chromatid exchanges (SCEs) in human lymphocytes. We found that N,N-diethylaniline significantly
Yongxia Zhang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 85(1), 134-138 (2011-11-01)
In this letter, we report the first observation of metal-enhanced exciplex fluorescence, observed from anthracene in the presence of diethylaniline. Anthracene in the presence of diethylaniline in close proximity to Silver Island Films (SIFs) shows enhanced monomer and exciplex emission

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