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632929

2-(Methylthio)ethylamine

Name: 2-(Methylthio)ethylamine
Brand: ALDRICH

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

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24882526

EC Number:

242-412-5

Beilstein/REAXYS Number:

1731099

MDL number:

MFCD00014825

Assay:

97%

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Properties

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

Description

pictograms

GHS02,GHS05

signalword

Danger

hcodes

H226,H314

pcodes

P210 - P233 - P240 - P280 - P303 + P361 + P353 - P305 + P351 + P338

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk

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

Regulatory Information

危险化学品

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Selective Preparation of a Heteroleptic Cyclometallated Ruthenium Complex Capable of Undergoing Photosubstitution of a Bidentate Ligand.

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

Cancer Stem Cell and Bulk Cancer Cell Active Copper(II) Complexes with Vanillin Schiff Base Derivatives and Naproxen.

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

Global Trade Item Number

SKU	GTIN
632929-1G	04061832721460
632929-5G	04061832721477