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W527505

Sigma-Aldrich

Ethanethiol solution

10 wt. % in propylene glycol

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About This Item

Empirical Formula (Hill Notation):
C2H6S
Molecular Weight:
62.13
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
12.017

biological source

synthetic

concentration

10 wt. % in propylene glycol

refractive index

n20/D 1.434

bp

187.7 °C

application(s)

flavors and fragrances

organoleptic

alliaceous

SMILES string

CCS

InChI

1S/C2H6S/c1-2-3/h3H,2H2,1H3

InChI key

DNJIEGIFACGWOD-UHFFFAOYSA-N

pictograms

FlameEnvironment

signalword

Danger

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

<-4.0 °F - closed cup

flash_point_c

< -20 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Vladimir Liberman et al.
Nanoscale, 7(25), 11013-11023 (2015-06-05)
In this paper, we report on a method to probe the breakdown of the organophosphate (OP) simulants o,s-diethyl methyl phosphonothioate (OSDMP) and demeton S by the enzyme organophosphorous hydrolase (OPH) in a microfluidic device by surface enhanced Raman spectroscopy (SERS).
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Free standing and strong odor-removing composite films of cellulose nanofibrils (CNF) with a high content of nanoporous zeolite adsorbents have been colloidally processed. Thermogravimetric desorption analysis (TGA) and infrared spectroscopy combined with computational simulations showed that commercially available silicalite-1 and
Hung V Le et al.
Journal of environmental quality, 44(5), 1523-1529 (2015-10-06)
Odorous emissions from agricultural and waste management operations can cause annoyance to local populations. Volatile sulfur compounds (VSCs) are dominant odorants that are often lost during collection using sample bags. The degree of VSC losses depends on factors such as
A Vasanits-Zsigrai et al.
Journal of chromatography. A, 1394, 81-88 (2015-04-05)
Quantification, stability and unique spectroscopic properties of indolinyl-caged glutamates (ICGs), with the o-phthalaldehyde-3-mercaptopropionic acid (OPA-MPA) reagent, were described, at first. As new principle to the field, reactivity and stoichiometry of variously substituted OPA-MPA derivatized ICGs, such as 4-methoxy-7-nitroindolinyl-(MNI-Glu), 4-methoxy-5,7-dinitroindolinyl-(DNI-Glu), 2-dimethylamino-propoxy

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