Skip to Content
Merck
All Photos(1)

Key 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


About This Item

Linear Formula:
(CH3)2NCH2N(CH3)2
CAS Number:
Molecular Weight:
102.18
Beilstein:
1731946
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

Pictograms

FlameCorrosion

Signal Word

Danger

Hazard Statements

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

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

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