Skip to Content
Merck
CN

422827

N-Methyl-4,4′-methylenedianiline

97%

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
CH3NHC6H4CH2C6H4NH2
CAS Number:
Molecular Weight:
212.29
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI

1S/C14H16N2/c1-16-14-8-4-12(5-9-14)10-11-2-6-13(15)7-3-11/h2-9,16H,10,15H2,1H3

SMILES string

CNc1ccc(Cc2ccc(N)cc2)cc1

InChI key

DEAOXXGXJLMFAS-UHFFFAOYSA-N

assay

97%

form

solid

mp

61-63 °C (lit.)

General description

N-Methyl-4,4′-methylenedianiline (4-(4-aminobenzyl)-N-methylaniline) is a 4,4′-methylenedianiline derivative. It has been synthesized by the methylation of 4,4′-methylenedianiline using formaldehyde and characterized by 1H NMR and mass spectrometry. It has been reported to be the one of the urinary metabolites during the in vivo metabolism of 4,4′-[14C]- methylenebis(N,N-dimethyl)benzamine (reduced Michler′s ketone, RMK) in Osborne-Mendel rats.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

D J McCarthy et al.
Cancer research, 42(9), 3475-3479 (1982-09-01)
Studies on the in vivo and in vitro disposition of 4,4'-[14C]-methylenebis(N,N-dimethyl)benzamine (reduced Michler's ketone, RMK) were performed. Osborne-Mendel rats retained, after 24 hr, 78% of a p.o. dose of [14C]RMK. At 24 hr after an i.p. dose, fat, liver, and

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