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Merck
CN

506818

Ethanethiol (ethyl mercaptan)

PESTANAL®, analytical standard

Synonym(s):

Ethanethiol, Ethyl mercaptan, Mercaptan C2

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About This Item

Linear Formula:
C2H5SH
CAS Number:
75-08-1
Molecular Weight:
62.13
EC Number:
200-837-3
UNSPSC Code:
12352200
PubChem Substance ID:
24873392
Beilstein/REAXYS Number:
773638
MDL number:
MFCD00004887

Key Documents

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InChI key

DNJIEGIFACGWOD-UHFFFAOYSA-N

InChI

1S/C2H6S/c1-2-3/h3H,2H2,1H3

SMILES string

CCS

grade

analytical standard

vapor density

2.1 (vs air)

vapor pressure

8.51 psi ( 20 °C)

product line

PESTANAL®

CofA

current certificate can be downloaded

autoignition temp.

570 °F

expl. lim.

18.2 %

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

refractive index

n20/D 1.4306 (lit.)

bp

35 °C (lit.)

density

0.839 g/mL at 25 °C (lit.)

application(s)

agriculture
environmental

format

neat

storage temp.

2-8°C

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Liq. 1

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

-49.0 °F - closed cup

flash_point_c

-45 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
MKCJ9048
MKBT4913V
MKBP7942V
LB90135V
LB89499V

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Jiangyao Chen et al.
Journal of hazardous materials, 190(1-3), 416-423 (2011-04-20)
A series of adsorptive photocatalysts, combined titania-montmorillonite-silica were synthesized. The resultant photocatalysts consisted of more and more spherically agglomerated TiO(2) particles with increasing of TiO(2) content, and anatase was the only crystalline phase with nano-scale TiO(2) particles. With increasing of
R Hanczkó et al.
Journal of chromatography. A, 1163(1-2), 25-42 (2007-07-04)
The main aims of this work were (a) to present the characteristics and stability of the o-phthalaldehyde (OPA)-ethanethiol (ET) derivatives of 22 amino acids, including the believed-to-be less stable OPA derivatives providing glycine, gamma-aminobutyric acid, beta-alanine, histidine, ornithine, lysine and
Takashi Kaneta et al.
Electrophoresis, 32(9), 1061-1067 (2011-03-31)
Previously, we have demonstrated postcolumn derivatization of proteins separated by capillary sieving electrophoresis (CSE), in which naphthalene-2,3-dicarbaldehyde was employed as a fluorogenic labeling reagent. Standard proteins separated by CSE were reacted with naphthalene-2,3-dicarbaldehyde in the presence of 2-mercaptoethanol (2-ME) which
Edmanuel Torres et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 12(5), 999-1009 (2011-03-12)
The translational and orientational potential energy surfaces (PESs) of n-alkanethiols with up to four carbon atoms are studied for (√(3)×√(3))R30° self-assembled monolayers (SAMs). The PESs indicate that methanethiol may form SAM structures that are not accessible for long-chain thiols. The
Natalie J Galant et al.
The journal of physical chemistry. A, 113(32), 9138-9149 (2009-09-02)
First principle quantum molecular computations have been carried out at the B3LYP/6-31G(d,p) and G3MP2B3 levels of theory on ethyl mercaptan and diethyl disulfide to study their full conformational space. The consequences of molecular axis chirality for the potential energy hypersurface
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