Skip to Content
Merck
All Photos(1)

Documents

690953

Sigma-Aldrich

N,N,N′,N′-Tetramethylguanidine

≥99.0% (GC)

Synonym(s):

1,1,3,3-Tetramethylguanidine

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

About This Item

Linear Formula:
(CH3)2NC(=NH)N(CH3)2
CAS Number:
80-70-6
Molecular Weight:
115.18
Beilstein:
969608
EC Number:
201-302-7
MDL number:
MFCD00008323
UNSPSC Code:
12352100
PubChem Substance ID:
329761375
NACRES:
NA.22

Assay

≥99.0% (GC)

form

liquid

impurities

≤0.50% water

color

APHA: ≤150

bp

162-163 °C (lit.)

density

0.916 g/mL at 20 °C (lit.)

SMILES string

CN(C)C(=N)N(C)C

InChI

1S/C5H13N3/c1-7(2)5(6)8(3)4/h6H,1-4H3

InChI key

KYVBNYUBXIEUFW-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

N,N,N′,N′-Tetramethylguanidine can be used to synthesize:
  • dinucleoside phosphotriester1
  • 1,1,3,3-tetramethylguanidinium 2-ethylhexoate2
  • tetramethylguanidine ionic liquid (TMG IL)3

Signal Word

Danger

Hazard Statements

H226,H290,H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

122.0 °F - closed cup

Flash Point(C)

50 °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

Synthesis and thermal characterization of novel poly (tetramethylsilanthrylenesiloxane) and poly (tetramethylsilphenanthrylenesiloxane) derivatives.
Sato I, et al.
Polymer Bull., 59(5), 607-617 (2007)
Deoxyribonucleoside cyclic N-acylphosphoramidites as a new class of monomers for the stereocontrolled synthesis of oligothymidylyl-and oligodeoxycytidylyl-phosphorothioates.
Wilk A, et al.
Journal of the American Chemical Society, 122(10), 2149-2156 (2000)
Tetramethyl guanidinium chlorosulfonate as a highly efficient and recyclable organocatalyst for the preparation of bis (indolyl) methane derivatives.
Kalla R, et al.
Catalysis Communications, 57, 55-59 (2014)
G V S M Carrera et al.
Faraday discussions, 183, 429-444 (2015-09-22)
In this report, novel systems, based on highly abundant saccharides, D-mannose, D-glucose, β-cyclodextrin, alginic acid and mannitol, in combination with an organic superbase, tetramethylguanidine (TMG) or 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), are studied for carbon dioxide capture. With D-mannose and D-glucose, several ratios

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