Skip to Content
Merck
All Photos(4)

Key Documents

More Documents

M44451

Sigma-Aldrich

4,4′-Methylenebis(N,N-dimethylaniline)

98%

Synonym(s):

N,N,N′,N′-Tetramethyl-4,4′-diaminodiphenylmethane, N,N,N′,N′-Tetramethyl-4,4′-methylenedianiline, Arnolds base, Michlers base

Sign Into View Organizational & Contract Pricing
All Photos(4)

About This Item

Linear Formula:
CH2[C6H4N(CH3)2]2
CAS Number:
101-61-1
Molecular Weight:
254.37
Beilstein:
479956
EC Number:
202-959-2
MDL number:
MFCD00008317
UNSPSC Code:
12171500
PubChem Substance ID:
24896922
NACRES:
NA.47

Quality Level

100

Assay

98%

form

powder, crystals or chunks

mp

88-89 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

CN(C)c1ccc(Cc2ccc(cc2)N(C)C)cc1

InChI

1S/C17H22N2/c1-18(2)16-9-5-14(6-10-16)13-15-7-11-17(12-8-15)19(3)4/h5-12H,13H2,1-4H3

InChI key

JNRLEMMIVRBKJE-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

4,4′-Methylenebis(N,N-dimethylaniline) is an intermediate in dye manufacture and works as a reagent for the determination of lead. It is suitable for the qualitative assay of cyanogens.

Application

4,4′-Methylenebis(N,N-dimethylaniline) has been used to check the production of hydrogen cyanide by bacteria.
4,4′-Methylenebis(N,N-dimethylaniline) has been used as a component in the preparation of Feigl-Anger paper for visualizing HCN release. It may also be suitable for the preparation and characterization of inclusion complex with β-cyclodextrin.

Biochem/physiol Actions

4,4′-Methylenebis(N,N-dimethylaniline) is used in the adduct purification of precursors. It is used as an intermediate in the preparation of its hydrochloric salt.

Pictograms

Health hazardEnvironment
GHS08,GHS09

Signal Word

Danger

Hazard Statements

H350 - H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

352.4 °F - closed cup

Flash Point(C)

178 °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?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

The multiple strategies of an insect herbivore to overcome plant cyanogenic glucoside defence
Pentzold S, et al.
Testing, 9(3), e91337-e91337 (2014)
Eighth Annual Report on Carcinogens (1999)
Investigation on inter molecular complexation between 4, 4?-methylene-bis (N, N-dimethylaniline) and beta-cyclodextrin: Preparation and characterization in aqueous medium and solid state
Periasamy R, et al.
Journal of Molecular Structure, 1080(3), 69-79 (2015)
Cassava flour and starch: progress in research and development (1996)
Is the ability of biocontrol fluorescent pseudomonads to produce the antifungal metabolite 2,4-diacetylphloroglucinol really synonymous with higher plant protection?
Rezzonico F
The New phytologist, 173, 861-861 (2007)
View All Related Papers

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