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MilliporeSigma

A34201

Allyl methyl sulfide

98%

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$96.05

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About This Item

Linear Formula:
H2C=CHCH2SCH3
CAS Number:
10152-76-8
Molecular Weight:
88.17
NACRES:
NA.22
PubChem Substance ID:
24890770
UNSPSC Code:
12352100
EC Number:
233-422-0
MDL number:
MFCD00008657

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Product Name

Allyl methyl sulfide, 98%

InChI key

NVLPQIPTCCLBEU-UHFFFAOYSA-N

InChI

1S/C4H8S/c1-3-4-5-2/h3H,1,4H2,2H3

SMILES string

CSCC=C

assay

98%

form

liquid

refractive index

n20/D 1.4714 (lit.)

bp

91-93 °C (lit.)

density

0.803 g/mL at 25 °C (lit.)

storage temp.

2-8°C

Quality Level

200

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This Item
303593M81705128252
Allyl methyl sulfide 98%

Sigma-Aldrich

A34201

Allyl methyl sulfide

Trimethylsulfonium methyl sulfate 98%

Sigma-Aldrich

303593

Trimethylsulfonium methyl sulfate

Dimethyl sulfone 98%

Sigma-Aldrich

M81705

Dimethyl sulfone

Ethylene sulfide 98%

Sigma-Aldrich

128252

Ethylene sulfide

assay

98%

assay

98%

assay

98%

assay

98%

Quality Level

200

Quality Level

100

Quality Level

200

Quality Level

200

density

0.803 g/mL at 25 °C (lit.)

density

-

density

-

density

1.01 g/mL at 25 °C (lit.)

refractive index

n20/D 1.4714 (lit.)

refractive index

-

refractive index

-

refractive index

n20/D 1.495 (lit.)

storage temp.

2-8°C

storage temp.

-

storage temp.

-

storage temp.

−20°C

bp

91-93 °C (lit.)

bp

-

bp

238 °C (lit.)

bp

55-56 °C (lit.)

pictograms

Flame
GHS02

signalword

Danger

hcodes

H225

Hazard Classifications

Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

64.4 °F - closed cup

flash_point_c

18 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCBR9403V
1432973V
00508012V
1432973
00508012

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M M Reicks et al.
Nutrition and cancer, 25(3), 241-248 (1996-01-01)
Garlic organosulfur compounds exert chemopreventive effects at several organ sites in rodents after administration of chemical carcinogens, possibly by inhibiting carcinogen activation via cytochrome P-450-mediated oxidative metabolism. It has been suggested that the variability in potency of tumor inhibition by
Destiny M Davenport et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 43(12), 1753-1762 (2005-07-08)
Organosulfur compounds (OSCs) derived from garlic have been studied for the ability to inhibit experimental cancer in various animal models, primarily through modification of carcinogen detoxification enzymes, such as cytochrome P450 (CYP) enzymes. OSCs vary in structural and physical properties
M K Kwak et al.
Biochemical pharmacology, 47(3), 531-539 (1994-02-09)
Cytochrome P4502E1 (CYP2E1) is active in both detoxication and activation of small organic molecules. The effects of organosulfur compounds including allylsulfide (AS), allylmercaptan (AM) and allylmethylsulfide (AMS) on the expression of CYP2E1 were examined in rats. 4-Nitrophenol, aniline hydroxylase and
Shelli F Farhadian et al.
Physiology & behavior, 105(2), 544-553 (2011-09-29)
The sensation of hunger after a period of fasting and of satiety after eating is crucial to behavioral regulation of food intake, but the biological mechanisms regulating these sensations are incompletely understood. We studied the behavioral and physiological adaptations to
Amalia Z Berna et al.
Journal of breath research, 12(4), 046014-046014 (2018-08-22)
We previously showed that thioether levels in the exhaled breath volatiles of volunteers undergoing controlled human malaria infection (CHMI) with P. falciparum increase as infection progresses. In this study, we show that thioethers have diurnal cyclical increasing patterns and their
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