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Merck

W347809

Sigma-Aldrich

1-Butanethiol

≥98%

Sinónimos:

Butyl mercaptan, Mercaptan C4

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About This Item

Fórmula lineal:
CH3(CH2)3SH
Número de CAS:
Peso molecular:
90.19
FEMA Number:
3478
Beilstein/REAXYS Number:
1730908
EC Number:
Council of Europe no.:
526
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
12.010
NACRES:
NA.21

biological source

synthetic

Quality Level

grade

Kosher

agency

meets purity specifications of JECFA

vapor density

3.1 (vs air)

vapor pressure

83 mmHg ( 37.7 °C)

assay

≥98%

refractive index

n20/D 1.443 (lit.)

bp

98 °C (lit.)

mp

−116 °C (lit.)

density

0.842 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

sulfurous

SMILES string

CCCCS

InChI

1S/C4H10S/c1-2-3-4-5/h5H,2-4H2,1H3

InChI key

WQAQPCDUOCURKW-UHFFFAOYSA-N

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General description

1-Butanethiol is a volatile sulfur-containing odorous compound that is reported to occur in skunk oil.

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

53.6 °F - closed cup

flash_point_c

12 °C - closed cup

ppe

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


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

The history of skunk defensive secretion research.
Wood WF
The Chemical Educator, 4(2), 44-50 (1999)
Nicole W G Smits et al.
Inorganic chemistry, 58(19), 13007-13019 (2019-09-25)
The structure of the copper complex of the 6-((1-butanethiol)oxy)-tris(2-pyridylmethyl)amine ligand (Cu-tmpa-O(CH2)4SH) anchored to a gold surface has been investigated. To enable covalent attachment of the complex to the gold surface, a heteromolecular self-assembled monolayer (SAM) of butanethiol and a thiol-substituted
W C Thomas et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 8(2), 170-178 (1987-02-01)
n-Butyl mercaptan (n-BM) is used as a solvent and a chemical intermediate. Pregnant Charles River CD-1 mice and COBS CD rats were randomly assigned to a control group and to three n-BM-exposed groups of 25 rats and 25 mice each.
Bob Muir et al.
Journal of chromatography. A, 1068(2), 315-326 (2005-04-16)
Thermal desorption with gas chromatography-mass spectrometry (TD-GC-MS) remains the technique of choice for analysis of trace concentrations of analytes in air samples. This paper describes the development and application of a method for analysing the vesicant compounds sulfur mustard and
Huili Zhang et al.
Talanta, 82(2), 733-738 (2010-07-07)
This work proposed a gas sensor for the determination of tert-butyl mercaptan, one of the highly toxic volatile sulfur compounds, which was based on cataluminescence emission during its catalytic oxidation on the surface of nanosized V(2)O(5). The cataluminescence characteristics and

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