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Merck
CN

36631

Supelco

阿特拉津-2-羟基

PESTANAL®, analytical standard

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别名:
2-羟基莠去津
经验公式(希尔记法):
C8H15N5O
CAS号:
分子量:
197.24
Beilstein:
5870987
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

agriculture
environmental

格式

neat

SMILES字符串

CCNc1nc(O)nc(NC(C)C)n1

InChI

1S/C8H15N5O/c1-4-9-6-11-7(10-5(2)3)13-8(14)12-6/h5H,4H2,1-3H3,(H3,9,10,11,12,13,14)

InChI key

NFMIMWNQWAWNDW-UHFFFAOYSA-N

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相关类别

一般描述

Atrazine-2-hydroxy is a non-herbicidal, primary photoproduct obtained upon hydrolytic dechlorination of atrazine.

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

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Anaerobic degradation of atrazine
Boopathy R, et al.
International Biodeterioration & Biodegradation, 119, 626-630 (2017)
The Triazine Herbicides (2011)
Milan Hutta et al.
Journal of separation science, 29(13), 1977-1987 (2006-10-05)
A well established method of direct injection of larger than conventional sample volumes ranging from 0.1 mL to 10 mL in HPLC is the injection valve method in which a loop of tubing is totally or partially filled with sample.
Susan C Laws et al.
Toxicological sciences : an official journal of the Society of Toxicology, 76(1), 190-200 (2003-09-13)
We showed previously that the chlorotriazine herbicide, atrazine (ATR), delays the onset of pubertal development in female rats. ATR and its biotransformation by-products are present in soil and groundwater. Since current maximum contaminant levels are set only for ATR, it
P C Das et al.
Toxicological sciences : an official journal of the Society of Toxicology, 59(1), 127-137 (2001-01-03)
The effects of four major chlorotriazine metabolites on the constitutive synthesis of the catecholamines dopamine (DA) and norepinephrine (NE) were examined, using undifferentiated PC12 cells. NE release and intracellular DA and NE concentrations were quantified, for up to 24 h

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