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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
分類程式碼代碼:
41116105

等級

certified reference material
TraceCERT®

agency

EPA 8031

產品線

TraceCERT®

CofA

current certificate can be downloaded

特點

standard type calibration

包裝

ampule of 1 mL

濃度

5000 μg/mL in methanol

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

格式

single component solution

儲存溫度

2-8°C

InChI

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

InChI 密鑰

NLHHRLWOUZZQLW-UHFFFAOYSA-N

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一般說明

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

應用

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

其他說明

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.

法律資訊

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

訊號詞

Danger

危險分類

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

標靶器官

Eyes,Central nervous system

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

49.5 °F - closed cup

閃點(°C)

9.7 °C - closed cup


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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
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
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
Tandem catalytic acrylonitrile cross-metathesis and hydrogenation of nitriles with ruthenium catalysts: direct access to linear α,ω-aminoesters from renewables.
Xiaowei Miao et al.
ChemSusChem, 5(8), 1410-1414 (2012-06-19)

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