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T21407

Sigma-Aldrich

N,N,N′,N′-Tetramethyldiaminomethane

99%

Synonym(s):

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

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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

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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)

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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

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