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632929

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:
1731099
EC Number:
242-412-5
MDL number:
MFCD00014825
UNSPSC Code:
12352100
PubChem Substance ID:
24882526
NACRES:
NA.22

Quality Level

100

Assay

97%

refractive index

n20/D 1.495 (lit.)

bp

146-149 °C (lit.)

density

0.98 g/mL at 20 °C (lit.)

functional group

amine
thioether

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

Signal Word

Danger

Hazard Statements

H226,H314

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

96.8 °F - closed cup

Flash Point(C)

36 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBL2461
STBL0204
STBK7892
STBK7891
STBK5018

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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
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

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