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P53209

Sigma-Aldrich

Propylene sulfide

≥96%

Sinónimos:

Methylthiirane

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About This Item

Fórmula empírica (notación de Hill):
C3H6S
Número de CAS:
1072-43-1
Peso molecular:
74.14
Beilstein/REAXYS Number:
383559
EC Number:
214-007-3
MDL number:
MFCD00005160
UNSPSC Code:
12352100
PubChem Substance ID:
24898621

assay

≥96%

refractive index

n20/D 1.475 (lit.)

bp

72-75 °C (lit.)

density

0.946 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CC1CS1

InChI

1S/C3H6S/c1-3-2-4-3/h3H,2H2,1H3

InChI key

MBNVSWHUJDDZRH-UHFFFAOYSA-N

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pictograms

FlameSkull and crossbones
GHS02,GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

50.0 °F - closed cup

flash_point_c

10 °C - closed cup

ppe

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

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Massimiliano Valentini et al.
Journal of the American Chemical Society, 126(7), 2142-2147 (2004-02-20)
We report the application of the pulse gradient spin-echo (PGSE) NMR technique (PGSE NMR) to the analysis of large colloidal materials, specifically vesicles formed from macromolecular amphiphiles and nanoparticles. Measurements of size and size distribution were demonstrated to be comparable
Michael-Rock Goldsmith et al.
Physical chemistry chemical physics : PCCP, 8(1), 63-67 (2006-02-17)
Using a dissymmetrically-perturbed particle-in-a-box model, we demonstrate that the induced optical activity of chiral monolayer protected clusters, such as Whetten's Au28(SG)16 glutathione-passivated gold nanoclusters (J. Phys. Chem. B, 2000, 104, 2630-2641), could arise from symmetric metal cores perturbed by a
J P Bearinger et al.
Nature materials, 2(4), 259-264 (2003-04-12)
Alkanethiolates have been widely used as chemisorbates to modify gold surfaces, in spite of their relatively poor oxidative stability. We introduce gold-chemisorbing block copolymers bearing an anchoring block of poly(propylene sulphide) (PPS), selected in the expectation of greater stability. These
T Matsuda et al.
Cancer letters, 86(2), 229-234 (1994-11-11)
Two organosulfur compounds, methyl propyl disulfide (MPD) and propylene sulfide (PS) from garlic and onions, were studied for their modifying effects on hepatocarcinogenesis in the F344 rats. Modifying potential was scored by comparing the number and area per cm2 of
Cong-Duan Vo et al.
Macromolecular rapid communications, 34(2), 156-162 (2013-01-16)
We report for the first time the combination of ATRP and ring-opening episulfide polymerization as a means to synthesize polysulfide-based low-dispersity amphiphilic block copolymers. The most significant finding is the possibility to perform ATRP under mild conditions using poly(propylene sulfide)
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