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40003

Supelco

Acrylonitrile solution

certified reference material, 5000 μg/mL in methanol

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About This Item

Formule empirique (notation de Hill):
C3H3N
Numéro CAS:
107-13-1
Poids moléculaire :
53.06
Code UNSPSC :
41116105

Qualité

certified reference material
TraceCERT®

Agence

EPA 8031

Gamme de produits

TraceCERT®

CofA (certificat d'analyse)

current certificate can be downloaded

Caractéristiques

standard type calibration

Conditionnement

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

Température de stockage

2-8°C

InChI

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

Clé InChI

NLHHRLWOUZZQLW-UHFFFAOYSA-N

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Description générale

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.

Autres remarques

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.

Informations légales

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

Pictogrammes

FlameSkull and crossbonesHealth hazard
GHS02,GHS06,GHS08

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Eyes,Central nervous system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

49.5 °F - closed cup

Point d'éclair (°C)

9.7 °C - closed cup

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
LRAD6036
LRAC8478
LRAC4171
LRAB8930
XA12783V

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Si vous avez besoin d'une version particulière, vous pouvez rechercher un certificat spécifique par le numéro de lot.

Rechercher un(e) COA

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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
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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