Skip to Content
Merck
All Photos(1)

Key Documents

41661

Sigma-Aldrich

1,3-Dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone

absolute, over molecular sieve (H2O ≤0.05%), ≥99.0% (GC)

Synonym(s):

1,3-Dimethyl-2-oxohexahydropyrimidine, N,N′-Dimethylpropylene urea, DMPU

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C6H12N2O
CAS Number:
Molecular Weight:
128.17
Beilstein:
110562
EC Number:
MDL number:
UNSPSC Code:
12352115
PubChem Substance ID:
NACRES:
NA.22

grade

absolute

Quality Level

Assay

≥99.0% (GC)

form

liquid

quality

over molecular sieve (H2O ≤0.05%)

refractive index

n20/D 1.488 (lit.)
n20/D 1.489

bp

146 °C/44 mmHg (lit.)

density

1.06 g/mL at 25 °C (lit.)

SMILES string

CN1CCCN(C)C1=O

InChI

1S/C6H12N2O/c1-7-4-3-5-8(2)6(7)9/h3-5H2,1-2H3

InChI key

GUVUOGQBMYCBQP-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

1,3-Dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU) can be used as a:
  • Solvent in the synthesis of 1-aryl-3,4,5-substituted pyrazoles by cyclocondensation of 1,3-diketones with arylhydrazine hydrochlorides.
  • Chelating solvent in the trifluoromethylation of activated and non-activated halogenated double bonds.
  • Ligand in ortho-alkylation of secondary benzamide catalyzed by cobalt.

Other Notes

Aprotic, dipolar solvent, which is an excellent replacement of the carcinogenic HMPA as cosolvent for highly reactive nucleophiles and bases. High Z-selectivity in enolate formation; DMPU was shown to be non-mutagenic and safe.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

249.8 °F - closed cup

Flash Point(C)

121 °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

Efficient Trifluoromethylation of Activated and Non-Activated Alkenyl Halides by Using (Trifluoromethyl) trimethylsilane.
Hafner A and Braese S
Advanced Synthesis & Catalysis, 353(16), 3044-3048 (2011)
anon.
Chimia, 39, 147-147 (1985)
Cobalt-catalyzed ortho-alkylation of secondary benzamide with alkyl chloride through directed C- H bond activation.
Chen Q, et al.
Journal of the American Chemical Society, 133(3), 428-429 (2010)
R.E. Ireland et al.
The Journal of Organic Chemistry, 56, 650-650 (1991)
Efficient Trifluoromethylation of Activated and Non-Activated Alkenyl Halides by Using (Trifluoromethyl) trimethylsilane.
Hafner A and Braese S
advanced synthesis and catalysis, 353(16), 3044-3048 (2011)

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