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40327

Supelco

Vinyl acetate solution

certified reference material, 5000 μg/mL in acetonitrile

Synonim(y):

Acetoxyethylene

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About This Item

Numer CAS:
108-05-4
Numer WE:
200-835-2
Kod UNSPSC:
41116105

klasa czystości

certified reference material
TraceCERT®

linia produktu

TraceCERT®

Certyfikat analizy

current certificate can be downloaded

opakowanie

ampule of 1 mL

stężenie

5000 μg/mL in acetonitrile

metody

HPLC: suitable
gas chromatography (GC): suitable

Zastosowanie

cleaning products
cosmetics
environmental
food and beverages
personal care
petroleum

format

single component solution

temp. przechowywania

2-8°C

InChI

1S/C4H6O2/c1-3-6-4(2)5/h3H,1H2,2H3

Klucz InChI

XTXRWKRVRITETP-UHFFFAOYSA-N

Powiązane kategorie

Opis ogólny

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

Zastosowanie

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

Inne uwagi

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.

Informacje prawne

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
This page may contain text that has been machine translated.

Piktogramy

FlameExclamation mark
GHS02,GHS07

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

H225,H302 + H312 + H332,H319

Klasyfikacja zagrożeń

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Kod klasy składowania

3 - Flammable liquids

Klasa zagrożenia wodnego (WGK)

WGK 2

Temperatura zapłonu (°F)

51.8 °F - closed cup

Temperatura zapłonu (°C)

11 °C - closed cup

Środki ochrony indywidualnej

Eyeshields, Faceshields, Gloves

Wybierz jedną z najnowszych wersji:

Certyfikaty analizy (CoA)

Lot/Batch Number
LRAC8350
LRAC0726
XA25696V
XA25684V
XA10634V

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Jeśli potrzebujesz konkretnej wersji, możesz wyszukać konkretny certyfikat według numeru partii lub serii.

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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

B Picquet-Varrault et al.
Environmental science & technology, 44(12), 4615-4621 (2010-05-25)
Vinyl acetate is widely used in industry. It has been classified as a high-production volume (HPV) chemical in the United States. To evaluate its impact on the environment and air quality, its atmospheric reactivity toward the three main tropospheric oxidants
Roberto M Risi et al.
Organic letters, 14(4), 1180-1182 (2012-02-07)
A highly atom-economical total synthesis of (+)-patulolide C has been accomplished in three steps from the known (2R)-8-nonyn-2-ol in 49% overall yield and 93% de. A Rh(I)-catalyzed asymmetric hydroformylation (AHF)/ intramolecular Wittig olefination cascade was utilized to set the C4-hydroxyl
Ellen Holthoff et al.
Sensors (Basel, Switzerland), 10(3), 1986-2002 (2010-01-01)
We report on the development of a microelectromechanical systems (MEMS)-scale photoacoustic sensor for the detection of trace gases. A mid-infrared quantum cascade laser (QCL) was used to determine detection limits for acetic acid, acetone, 1,4-dioxane, and vinyl acetate. The source
María B Blanco et al.
Environmental science & technology, 46(16), 8817-8825 (2012-07-18)
The products formed from the reactions of OH radicals with vinyl acetate and allyl acetate have been studied in a 1080 L quartz-glass chamber in the presence and absence of NO(x) using in situ FTIR spectroscopy to monitor the reactant
Ming-Cheng Lin et al.
Journal of biochemical and molecular toxicology, 25(5), 330-339 (2011-06-02)
Enantiomers of cis,cis-decahydro-2-naphthyl-N-n-butylcarbamate show stereo-specific inhibition for acetylcholinesterase and butyrylcholinesterase. For both inhibition reaction, (2S,4aR,8aS)-cis,cis-decahydro-2-naphthyl-N-n- butylcarbamate is more potent than (2R,4aS,8aR)-cis,cis-decahydro-2-naphthyl-N-n-butylcarbamate. Optically pure (2S,4aR,8aS)-(-)- and (2R,4aS,8aR)-(+)-cis,cis-decahydro-2-naphthols are resolved by the porcine pancreatic lipase-catalyzed acetylation of decahydro-2-naphthols with vinyl acetate. Absolute
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