MilliporeSigma
All Photos(1)

Documents

M54201

Sigma-Aldrich

2-(Methylthio)aniline

97%

Sign Into View Organizational & Contract Pricing

Synonym(s):
2-(Methylmercapto)aniline, 2-Aminothioanisole
Linear Formula:
CH3SC6H4NH2
CAS Number:
Molecular Weight:
139.22
Beilstein:
386211
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

refractive index

n20/D 1.624 (lit.)

bp

234 °C (lit.)

density

1.111 g/mL at 25 °C (lit.)

SMILES string

CSc1ccccc1N

InChI

1S/C7H9NS/c1-9-7-5-3-2-4-6(7)8/h2-5H,8H2,1H3

InChI key

WBRPQQSADOCKCH-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
250406144886M54503
2-(Methylthio)aniline 97%

Sigma-Aldrich

M54201

2-(Methylthio)aniline

3-(Methylthio)aniline 97%

Sigma-Aldrich

144886

3-(Methylthio)aniline

4-(Methylthio)aniline 97%

Sigma-Aldrich

M54503

4-(Methylthio)aniline

refractive index

n20/D 1.624 (lit.)

refractive index

n20/D 1.592 (lit.)

refractive index

n20/D 1.637 (lit.)

refractive index

n20/D 1.639 (lit.)

bp

234 °C (lit.)

bp

216-217 °C (lit.)

bp

163-165 °C/16 mmHg (lit.)

bp

272-273 °C (lit.)

density

1.111 g/mL at 25 °C (lit.)

density

1.226 g/mL at 25 °C (lit.)

density

1.13 g/mL at 25 °C (lit.)

density

1.119 g/mL at 25 °C (lit.)

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

> 113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Documents related to the products that you have purchased in the past have been gathered in the Document Library for your convenience.

Visit the Document Library

Difficulty Finding Your Product Or Lot/Batch Number?

Product numbers are combined with Pack Sizes/Quantity when displayed on the website (example: T1503-25G). Please make sure you enter ONLY the product number in the Product Number field (example: T1503).

Example:

T1503
Product Number
-
25G
Pack Size/Quantity

Additional examples:

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

enter as 1.000309185)

Having trouble? Feel free to contact Technical Service for assistance.

Lot and Batch Numbers can be found on a product's label following the words 'Lot' or 'Batch'.

Aldrich Products

  • For a lot number such as TO09019TO, enter it as 09019TO (without the first two letters 'TO').

  • For a lot number with a filling-code such as 05427ES-021, enter it as 05427ES (without the filling-code '-021').

  • For a lot number with a filling-code such as STBB0728K9, enter it as STBB0728 without the filling-code 'K9'.

Not Finding What You Are Looking For?

In some cases, a COA may not be available online. If your search was unable to find the COA you can request one.

Request COA

Customers Also Viewed

Slide 1 of 3

1 of 3

8-Aminoquinoline 98%

Sigma-Aldrich

260789

8-Aminoquinoline

4-Aminothiophenol ≥97.0%

Sigma-Aldrich

422967

4-Aminothiophenol

2-Acetylpyridine ≥99%

Sigma-Aldrich

A21002

2-Acetylpyridine

Manisha Das et al.
Dalton transactions (Cambridge, England : 2003), 48(4), 1292-1313 (2019-01-05)
Rational ligand design approaches allowed {Cu2(μ-OH/OMe)} cores to be accommodated within μ-phenoxido bis(tetradentate) and μ-phenoxido bis(tridentate) ligands having thioether donors. The complexes [Cu2(μ-H2L1)(μ-OH)](ClO4)2·2H2O (1), [Cu2(μ-L2)(μ-OH)(OH2)](ClO4)2 (2a) and [Cu2(μ-L2)(μ-OCH3)(OH2)](ClO4)2 (2b) were obtained from an N2O3S2 donor set bearing the H3L1 ligand
Takashi Ikawa et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(19), 4320-4332 (2020-01-03)
Benzynes were selectively generated in situ from phenols and trapped regioselectively with potassium hexamethyldisilazide to form primary anilines following acidic workup. The direct conversion of a phenolic hydroxyl group into a free amino group is a useful method for the

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service