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Merck

112925

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847120
EC Number:
203-705-3
Beilstein/REAXYS Number:
1730908
MDL number:
MFCD00004905

Product Name

1-Butanethiol, 99%

SMILES string

CCCCS

InChI key

WQAQPCDUOCURKW-UHFFFAOYSA-N

InChI

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

vapor density

3.1 (vs air)

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

Quality Level

200

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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

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

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

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Certificates of Analysis (COA)

Lot/Batch Number
SHBN3171
SHBJ1782
SHBH3554V
SHBG6741V
SHBD3371V

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Pratik Gurnani et al.
Macromolecular bioscience, 18(10), e1800213-e1800213 (2018-08-08)
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.
Yinghui Chen et al.
Acta biomaterialia, 102, 384-393 (2019-12-04)
Surface modification to obtain high dispersion stability and biocompatibility is a key factor for bio-application of upconversion nanoparticles (UCNPs). A systematic study of UCNPs modified with four hydrophilic molecules separately, comparing their dispersion stability in biological buffers and cellular biocompatibility
X Wang et al.
Chemical science, 9(21), 4879-4891 (2018-06-19)
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
E Mather-Mihaich et al.
Comparative biochemistry and physiology. C, Comparative pharmacology and toxicology, 85(2), 427-432 (1986-01-01)
Indicators of free-radical or oxidant-mediated responses were quantified in channel catfish, Ictalurus punctatus, exposed to the organophosphorus herbicide DEF and its metabolite, n-butyl mercaptan (nBM). The activities of the antioxidant enzymes superoxide dismutase (SOD), glutathione peroxidase (GPX) and catalase did
Late acute, delayed neurotoxic and cholinergic effects of S,S,S-tributyl phosphorotrithioite (Merphos) in hens.
M B Abou-Donia et al.
Toxicology and applied pharmacology, 53(3), 439-457 (1980-05-01)
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