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Sigma-Aldrich

2-(Methylthio)ethylamine

97%

Synonym(s):

2-Aminoethyl methyl sulfide, S-Methylcysteamine

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About This Item

Linear Formula:
CH3SCH2CH2NH2
CAS Number:
18542-42-2
Molecular Weight:
91.18
Beilstein/REAXYS Number:
1731099
EC Number:
242-412-5
MDL number:
MFCD00014825
UNSPSC Code:
12352100
PubChem Substance ID:
24882526
NACRES:
NA.22

assay

97%

refractive index

n20/D 1.495 (lit.)

bp

146-149 °C (lit.)

density

0.98 g/mL at 20 °C (lit.)

SMILES string

CSCCN

InChI

1S/C3H9NS/c1-5-3-2-4/h2-4H2,1H3

InChI key

CYWGSFFHHMQKET-UHFFFAOYSA-N

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pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

hcodes

H226,H314

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

96.8 °F - closed cup

flash_point_c

36 °C - closed cup

ppe

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

Certificates of Analysis (COA)

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Jordi-Amat Cuello-Garibo et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(5), 1260-1268 (2018-10-16)
Cyclometallated ruthenium complexes typically exhibit red-shifted absorption bands and lower photolability compared to their polypyridyl analogues. They also have lower symmetry, which sometimes makes their synthesis challenging. In this work, the coordination of four N,S bidentate ligands, 3-(methylthio)propylamine (mtpa), 2-(methylthio)ethylamine
Chunxin Lu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(47), 11366-11374 (2017-06-29)
Four copper(II) complexes, 1-4 containing regioisomeric vanillin Schiff base derivatives and the nonsteroidal anti-inflammatory drug (NSAID), naproxen, were synthesised and characterised. All complexes effectively cleave DNA in cell-free systems, with 4 displaying the highest nuclease activity. DNA binding studies suggest

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