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Merck

40003

Supelco

丙烯腈 溶液

certified reference material, 5000 μg/mL in methanol

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About This Item

经验公式(希尔记法):
C3H3N
CAS号:
分子量:
53.06
MDL编号:
UNSPSC代码:
41116105

等级

certified reference material
TraceCERT®

Agency

EPA 8031

产品线

TraceCERT®

CofA

current certificate can be downloaded

特点

standard type calibration

包装

ampule of 1 mL

浓度

5000 μg/mL in methanol

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

包装形式

single component solution

储存温度

2-8°C

SMILES字符串

N#CC=C

InChI

1S/C3H3N/c1-2-3-4/h2H,1H2

InChI key

NLHHRLWOUZZQLW-UHFFFAOYSA-N

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一般描述

This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here

应用

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

其他说明

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

法律信息

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

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 - closed cup

闪点(°C)

9.7 °C - closed cup


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Danish J Malik et al.
PloS one, 7(8), e43354-e43354 (2012-08-24)
Novel carbon materials have been prepared by the carbonization of acrylonitrile (AN)/divinylbenzene (DVB) suspension porous copolymers having nominal crosslinking degrees in the range of 30-70% and obtained in the presence of various amounts of porogens. The carbons were obtained by
Pedro de la Torre et al.
Molecules (Basel, Switzerland), 17(10), 12072-12085 (2012-10-23)
(E)-2-(benzo[d]thiazol-2-yl)-3-heteroarylacrylonitriles are described as a new class of selective inhibitors of acetylcholinesterase (AChE). The most potent compound in the series exhibited good AChE inhibitory activity (IC₅₀ = 64 µM). Compound 7f was found to be more selective than galanthamine in
S Guedidi et al.
Enzyme and microbial technology, 51(6-7), 325-333 (2012-10-09)
A combined fluorescence analysis, involving the use of steady-state fluorescence and fluorescence anisotropy was used, allowing eliciting information about the structural changes induced on trypsin after exposure to membrane surfaces with diverse chemistry, designed through a layer-by-layer methodology. Using this
Hongwei Hou et al.
Analytical biochemistry, 430(1), 75-82 (2012-08-08)
The acrylonitrile metabolites 2-cyanoethylmercapturic acid (CEMA) and 2-hydroxyethylmercapturic acid (HEMA) have been determined in human urine using an automated column-switching procedure. A diluted sample was centrifuged just prior to being injected into a reusable precolumn packed with a restricted access
Yuchao Ma et al.
Journal of industrial microbiology & biotechnology, 39(10), 1421-1430 (2012-05-29)
Tolerance to various stresses is a key phenotype for cell catalysts, which are used widely in bioproduction of diverse valuable chemicals. Using the Rhodococcus ruber TH strain, which exhibits high nitrile hydratase activity, as the target cell catalyst for acrylamide

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