Skip to Content
Merck
All Photos(1)

Documents

T21407

Sigma-Aldrich

N,N,N′,N′-Tetramethyldiaminomethane

99%

Synonym(s):

N,N,N′,N′-Tetramethylmethanediamine, Bis(dimethylamino)methane

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
(CH3)2NCH2N(CH3)2
CAS Number:
51-80-9
Molecular Weight:
102.18
Beilstein:
1731946
EC Number:
200-124-7
MDL number:
MFCD00008328
UNSPSC Code:
12352100
PubChem Substance ID:
24900015
NACRES:
NA.22

Quality Level

200

Assay

99%

refractive index

n20/D 1.401 (lit.)

bp

85 °C (lit.)

density

0.749 g/mL at 25 °C (lit.)

SMILES string

CN(C)CN(C)C

InChI

1S/C5H14N2/c1-6(2)5-7(3)4/h5H2,1-4H3

InChI key

VGIVLIHKENZQHQ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Pictograms

FlameCorrosion
GHS02,GHS05

Signal Word

Danger

Hazard Statements

H225 - H314

Hazard Classifications

Flam. Liq. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

12.2 °F - closed cup

Flash Point(C)

-11 °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

Jie Wu et al.
ACS infectious diseases, 5(7), 1087-1104 (2019-04-25)
This article reports the rational medicinal chemistry of a natural product, agrimophol (1), as a new disruptor of intrabacterial pH (pHIB) homeostasis in Mycobacterium tuberculosis (Mtb). Through the systematic investigation of the structure-activity relationship of 1, scaffold-hopping of the diphenylmethane
Abdullah Alzahrani et al.
Organic & biomolecular chemistry, 16(22), 4108-4116 (2018-05-19)
The traditional thermal Mannich reaction is unsuitable for preparing polymerizable N-methylene amino substituted acrylamides and methacrylamides. Herein we provide a facile multi-gram high yield synthesis of these monomeric precursors to stimuli-responsive polymers by the addition of acrylamides and methacrylamides onto

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