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Merck

1466652

USP

N-Nitrosodiethylamine (NDEA)

United States Pharmacopeia (USP) Reference Standard

别名:

N-Ethyl-N-nitrosoethanamine, NDEA

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1 ML
$1,020.00

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预计发货时间2025年5月16日详情


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1 ML
$1,020.00

About This Item

经验公式(希尔记法):
C4H10N2O
CAS号:
分子量:
102.14
MDL编号:
UNSPSC代码:
41116107
NACRES:
NA.24

$1,020.00


预计发货时间2025年5月16日详情


获取大包装报价

包装

pkg of 1 mg

制造商/商品名称

USP

应用

pharmaceutical (small molecules)

包装形式

neat

储存温度

−20°C

SMILES字符串

N(N=O)(CC)CC

InChI

1S/C4H10N2O/c1-3-6(4-2)5-7/h3-4H2,1-2H3

InChI key

WBNQDOYYEUMPFS-UHFFFAOYSA-N

一般描述

This product is provided as delivered and specified by the USP Pharmacopoeia. For further information and support, including certificate/ product information sheets, please go to the website of the issuing Pharmacopoeia.

应用

N-Nitrosodiethylamine (NDEA) USP reference standard is intended for use only as specificallyprescribed in the United States Pharmacopoeia.

It is also used to prepare standard, standard stock, nitrosamineRS stock, Nitrosamine standards stock solution mixture, and sensitivity stocksolutions to determine NDEA impurity in drug substances and drug products(valsartan, irbesartan, and losartan potassium etc.) by chromatography methodaccording to the general chapter <1469> of United States Pharmacopeia.[1]

分析说明

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  

其他说明

This product is part of USP Biologics Program.
Sales restrictions may apply.

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Carc. 1B - Flam. Liq. 2 - STOT SE 1

靶器官

Eyes,Central nervous system

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

49.5 °F

闪点(°C)

9.7 °C


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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?1469? NITROSAMINE IMPURITIES
United States Pharmacopeia, 46(5) (2021)

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An overview of nitrosamine impurity testing, worldwide regulations, and key considerations in filter selection for sample preparation and analysis.

This application note describes the LC-MS-based quantitative analysis of known nitrosamine impurities following procedures 1 and 3 as given in USP general chapter <1469>.

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