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Merck

40003

Supelco

Acrylonitrile solution

certified reference material, 5000 μg/mL in methanol

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About This Item

Fórmula empírica (notación de Hill):
C3H3N
Número de CAS:
Peso molecular:
53.06
UNSPSC Code:
41116105

grade

certified reference material
TraceCERT®

Quality Level

agency

EPA 8031

product line

TraceCERT®

CofA

current certificate can be downloaded

feature

standard type calibration

packaging

ampule of 1 mL

concentration

5000 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

single component solution

storage temp.

2-8°C

InChI

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

InChI key

NLHHRLWOUZZQLW-UHFFFAOYSA-N

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General description

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

Application

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

Other Notes

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.

Legal Information

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

signalword

Danger

Hazard Classifications

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

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup


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S Guedidi et al.
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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
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)
Oscar Martinez et al.
The Journal of chemical physics, 138(9), 094316-094316 (2013-03-15)
The rotational spectrum of protonated vinyl cyanide, CH2CHCNH(+), a prototypical branched nitrile species and likely intermediate in astronomical sources and in the planetary atmosphere of Titan, has been detected in a pulsed-discharge supersonic molecular beam by means of Fourier transform
Dokyoung Kim et al.
Chemical communications (Cambridge, England), 48(54), 6833-6835 (2012-06-02)
Reaction-based fluorescent probes for monoamine oxidases A and B are developed based on a new two-photon absorbing compound and its precursor. The probes show turn-on fluorescence response to the enzymes owing to the two-photon absorbing compound produced by the enzymatic
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

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