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W221503

Butyl sulfide

≥95%, FG

Synonym(s):

Dibutyl sulfide, 1,1′-Thiobisbutane, Butyl sulfide, NSC 8460

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1 EACH

$58.00

1 KG

$210.00

4 KG

$484.00

8 KG

$959.00

$58.00


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About This Item

Linear Formula:
CH3(CH2)3S(CH2)3CH3
CAS Number:
Molecular Weight:
146.29
FEMA Number:
2215
Council of Europe no.:
484
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
12.007
EC Number:
208-870-5
NACRES:
NA.21
MDL number:
Beilstein/REAXYS Number:
1732829
Organoleptic:
green; sulfurous
Grade:
FG
Fragrance grade
Kosher
Biological source:
synthetic
Agency:
follows IFRA guidelines
meets purity specifications of JECFA
Food allergen:
no known allergens

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Product Name

Butyl sulfide, ≥95%, FG

SMILES string

CCCCSCCCC

InChI

1S/C8H18S/c1-3-5-7-9-8-6-4-2/h3-8H2,1-2H3

InChI key

HTIRHQRTDBPHNZ-UHFFFAOYSA-N

biological source

synthetic

grade

FG
Fragrance grade
Kosher

agency

follows IFRA guidelines
meets purity specifications of JECFA

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
FDA 21 CFR 172.515

vapor density

5.07 (vs air)

vapor pressure

5.17 mmHg ( 37.7 °C)

assay

≥95%

refractive index

n20/D 1.452 (lit.)

bp

188-189 °C (lit.)

mp

−76 °C (lit.)

density

0.838 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

organoleptic

green; sulfurous

Quality Level

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1 of 4

This Item
W218804W204218W274615
grade

FG, Kosher, Fragrance grade

grade

FG, Fragrance grade, Halal, Kosher

grade

FG, Fragrance grade, Halal, Kosher

grade

FG, Fragrance grade, Halal, Kosher, redistilled

organoleptic

green; sulfurous

organoleptic

apple; banana; green; fruity; sweet

organoleptic

garlic; horseradish; onion; sulfurous

organoleptic

cabbage; green; onion; vegetable; sulfurous; tomato

biological source

synthetic

biological source

synthetic

biological source

synthetic

biological source

synthetic

food allergen

no known allergens

food allergen

no known allergens

food allergen

no known allergens

food allergen

no known allergens

documentation

see Safety & Documentation for available documents

documentation

see Safety & Documentation for available documents

documentation

see Safety & Documentation for available documents

documentation

see Safety & Documentation for available documents

assay

≥95%

assay

≥97%

assay

≥97%

assay

≥99%

Application


  • Room-Temperature Synthesis of Thioether-Stabilized Ruthenium Nanocubes and Their Optical Properties.: This article presents a method for synthesizing thioether-stabilized ruthenium nanocubes at room temperature, using butyl sulfide as a stabilizing agent. The study details the optical properties of the nanocubes, which could have implications for their use in catalysis and materials science (Adams et al., 2023).

Biochem/physiol Actions

Taste at 5 ppm

General description

Butyl sulfide is a volatile sulfur compound that can be used as a flavoring agent.[1]

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

170.6 °F - closed cup

flash_point_c

77 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Burdock GA
Encyclopedia of Food and Color Additives, 1, 356-357 (1997)
Burdock GA
Encyclopedia of Food and Color Additives, 1, 356-357 (1997)
Abdul Karim-Talaq Mohammad et al.
Biomedical chromatography : BMC, 33(4), e4481-e4481 (2019-01-08)
A method for digestion of light and medium Iraqi crude oils (Basrah and Khanaken oils) using microwave-induced combustion (MIC) in closed vessels is described for the determination of Hg, Au, Cu, Al, Ca, Co, K, Mg, Si and Sr by
Stanisław Popiel et al.
Journal of hazardous materials, 157(2-3), 319-327 (2008-02-23)
A scheme of dibutyl sulfide (DBS) oxidation with ozone and generation of transitional products was determined in this study. The main identified intermediate product was dibutyl sulfoxide (DBSO), and the main end product of DBS oxidation was dibutyl sulfone (DBSO2).
The effect of dibutyl sulphide on hepatocytes studied by means of the isolated rat liver perfusion after preceding exposure to tetrachloromethane and phenobarbital in vivo.
O Nováková et al.
Acta Universitatis Carolinae. Medica, 27(1-2), 139-145 (1981-01-01)

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