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112925

Sigma-Aldrich

1-Butanethiol

99%

Synonym(s):

Butyl mercaptan, Mercaptan C4

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About This Item

Linear Formula:
CH3(CH2)3SH
CAS Number:
109-79-5
Molecular Weight:
90.19
Beilstein:
1730908
EC Number:
203-705-3
MDL number:
MFCD00004905
UNSPSC Code:
12352100
PubChem Substance ID:
24847120
NACRES:
NA.22

vapor density

3.1 (vs air)

Quality Level

200

vapor pressure

83 mmHg ( 37.7 °C)

Assay

99%

refractive index

n20/D 1.443 (lit.)

bp

98 °C (lit.)

mp

−116 °C (lit.)

density

0.842 g/mL at 25 °C (lit.)

functional group

thiol

SMILES string

CCCCS

InChI

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

InChI key

WQAQPCDUOCURKW-UHFFFAOYSA-N

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Application

1-Butanethiol is used as a model gaseous analyte for fast-responding membrane-free amperometric gas sensor.

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

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 Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

53.6 °F - closed cup

Flash Point(C)

12 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBN3171
SHBJ1782
SHBH3554V
SHBG6741V
SHBD3371V

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Current approaches to generate core-shell nanoparticles for biomedical applications are limited by factors such as synthetic scalability and circulatory desorption of cytotoxic surfactants. Developments in controlled radical polymerization, particularly in dispersed states, represent a promising method of overcoming these challenges.
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X Wang et al.
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Acidithiobacillus ferrooxidans, a chemolithoautotrophic Gram-negative bacterium, has a remarkable ability to obtain energy from ferrous iron oxidation at pH 2. Several metalloproteins have been described as being involved in this respiratory chain coupling iron oxidation with oxygen reduction. However, their
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.
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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