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P53209

Sigma-Aldrich

Propylene sulfide

≥96%

Synonym(s):

Methylthiirane

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About This Item

Empirical Formula (Hill Notation):
C3H6S
CAS Number:
1072-43-1
Molecular Weight:
74.14
Beilstein:
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

Signal Word

Danger

Hazard Statements

H225,H301,H315,H319,H332

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

50.0 °F - closed cup

Flash Point(C)

10 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBF8917V
BCBB2708V
BCBB2708
010706/1
04204KE

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Biomaterials: Stable antifouling surfaces.
Ralph G Nuzzo
Nature materials, 2(4), 207-208 (2003-04-12)
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)
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.
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