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Merck
CN

P53209

Propylene sulfide

≥96%

Synonym(s):

Methylthiirane

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About This Item

Empirical Formula (Hill Notation):
C3H6S
CAS Number:
Molecular Weight:
74.14
EC Number:
214-007-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
383559
MDL number:
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Product Name

Propylene sulfide, ≥96%

InChI key

MBNVSWHUJDDZRH-UHFFFAOYSA-N

InChI

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

SMILES string

CC1CS1

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

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pictograms

FlameSkull and crossbones

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

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

Regulatory Information

危险化学品
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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
Biomaterials: Stable antifouling surfaces.
Ralph G Nuzzo
Nature materials, 2(4), 207-208 (2003-04-12)
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
Masamichi Yamanaka et al.
Chemical communications (Cambridge, England), (15)(15), 1690-1691 (2004-07-28)
Three chiral guests in a cylindrical capsule led to six diastereomeric complexes.
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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