Page last updated: 2024-12-07

n,n'-dimethylpropyleneurea

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Description

n,n'-dimethylpropyleneurea (DMPU) is a colorless, odorless, hygroscopic liquid that is used as a solvent and a reagent in organic synthesis. It is a highly polar aprotic solvent, which means that it does not have a hydrogen atom attached to an electronegative atom. This property makes DMPU a good solvent for many organic reactions, as it does not interfere with the reaction mechanism. DMPU is also a good reagent for the synthesis of many organic compounds, such as amides, esters, and ethers. DMPU is a relatively inexpensive and readily available solvent, which makes it a popular choice for organic chemists. Its importance lies in its ability to dissolve a wide range of organic compounds, including polar and non-polar compounds. It is also a good solvent for many inorganic compounds. DMPU is studied for its ability to improve the solubility of organic compounds and its ability to promote certain organic reactions. DMPU is also used in the synthesis of pharmaceuticals, pesticides, and other chemicals. It is also used as a solvent in the production of polymers and plastics.'

N,N'-dimethylpropyleneurea: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID81646
CHEMBL ID12284
SCHEMBL ID82580
MeSH IDM0380300

Synonyms (100)

Synonym
tetrahydro-1,3-dimethyl-2(1h)pyrimidine
brn 0110562
n,n'-dimethyltrimethyleneurea
einecs 230-625-6
ccris 4322
tetrahydro-1,3-dimethyl-1h-pyrimidin-2-one
dimethylpropyleneurea
ec 230-625-6
dmpu
7226-23-5
2(1h)-pyrimidinone, tetrahydro-1,3-dimethyl-
2-pyrimidone,tetrahydro,1,3-dimethyl
1,3-dimethyltetrahydropyrimidin-2(1h)-one
inchi=1/c6h12n2o/c1-7-4-3-5-8(2)6(7)9/h3-5h2,1-2h
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone, 98%
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone, absolute, over molecular sieve (h2o <=0.03%), >=99.0% (gc)
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone
CHEMBL12284
AKOS005145503
D2014
n,n'-dimethylpropyleneurea
1,3-dimethyl-1,3-diazinan-2-one
A837469
EN300-82368
1,3-dimethyl-3,4,5,6-tetrahydro-2[1h]-pyrimidinone
n,n'-dimethylpropylene urea
FT-0606689
SCHEMBL82580
J-503925
1,3-dimethyl-2-oxohexahydropyrimidine
n,n'-dimethylproyleneurea
1,3-dimethyl-3,4,5,6-tetrahydro-2 [1h]-pyrimidinone
1,3-dimethyl-3,4,5,6-tetrahydropyrimidinone
1,3-dimethyl-3,4,5,6tetrahydro-2(1h)-pyrimidinone
1,3-dimethyl-tetrahydro-pyrimidin-2-one
1,3-dimethyltetrahydro-2(1h)-pyrimidone
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidone
1,3-dimethyl-3,4,5,6-tetrahydro-2 (1h)pyrimidinone
1,3-dimethyl-3,4,5,6-tetrahydro-(1h)-pyrimidin-2-one
1,3-di-methyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone
1,3-dimethyltetrahydro-2(1h)pyrimidinon
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrirnidinone
1,3-dimethyl-2,4,5,6-tetrahydro-2(1h)-pyrimidinone
1,3-dimethyl-tetrahydro-2-1h-pyrimidinone
1,3-dimethyltetrahydro-2-(1h)-pyrimidinone
1,3-di- methyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone
n,n'-dimethyl -1,4,5,6-tetrahydro-2-pyrimidone
1,3-dimethyl-3,4,5,6-tetrahydro-2-(1h)-pyrimidinone
1,3-dimethyl-3,4,5,6-tetrahydro 2(1h) pyrimidone
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinon
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)pyrimidinone
1,3-dimethyl -3,4,5,6-tetrahydro-2(1h)-pyrimidinone
1,3-dimethyl-3,4,5, 6-tetrahydro -2(1h)-pyrimidinone
dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone
n,n'-dimethyl-1,4,5,6-tetrahydro-2-pyrimidone
1,3-dimethyl-3,4,5,6-tetrahydro-2 (1h)-pyrimidone
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)- pyrimidinone
1,3-dimethyl tetrahydropyrimidin-2(1h)-one
1,3-dimethyl-3,4,5,6-tetrahydro 2 (1h)-pyrimidinone
1,3-dimethyl-3,4,5,6-tetrahydro-2 (1 h)-pyrimidinone
1,3-dimethyl-3,4,5,6-tetrahydro-2(1 h)-pyrimidinone
1,3-dimethyl-3,4,5,6-tetrahydropyrimidin-2-one
dimethylpropyl-eneurea
1,3-dimethyl-3,4,5,6-tetrahydro-2-pyrimidinone
1,3-dimethyl-tetrahydropyrimidin-2-one
1,3-dimethyl-3,4,5,6-tetrahydro2(1h)-pyrimidinone
1,3-dimethyltetrahydro-2-pyrimidinone
1,3-dimethyltetrahydro-2(1h)-pyrimidinone
1,3-dimethyl-3,4,5,6-tetrahydro- -2-(1h)-pyrimidone
1,3-dim-ethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone
1,3-dimethyl propylene urea
1,3-dimethyl-3,4,5,6-tetrahydro-2 (1h)-pyrimidinone
1,3-dimethyl-3,4,5,6-tetra-hydro-(1h)-pyrimidin-2-one
n, n'-dimethylpropyleneurea
1,3-dimethyl-tetrahydro -pyrimidin-2-one
1,3-dimethyl-3,4,5,6-tetrahydro-2-(1h)pyrimidone
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)pyrimdinone
1,3 dimethyl 3,4,5,6-tetrahydro-2-pyrimidone
STR03401
tetrahydro-1,3-dimethyl-2(1h)pyrimidin-2-onee
1,3-dimethyl-tetrahydro-2(1h)-pyrimidone
mfcd00006550
DTXSID3074575 ,
CS-W009128
P17490
F0001-1844
BCP25854
labotest-bb lt00848352 dmpu dimethylpropylene urea dimethyl(1,3-)-3,4,5,6-tetrahydro-2h-pyrimidone 1,3-dimet
Q416637
n,n-dimethyl-propylene-urea
AMY12538
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone (dmpu)
SY002520
1,3-dimethyltetrahydro-2-pyrimidone
n,n'-dimethylpropyleneurea (dmpu)
PB47348
1,3-dimethyl-2-oxohexahydropyrimidine, n,n'-dimethylpropylene urea, dmpu
1,3-dmethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone
Z1237078782
HY-Y0100
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (5)

Assay IDTitleYearJournalArticle
AID1570847Cytotoxicity against African green monkey Vero cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay2019ACS medicinal chemistry letters, Oct-10, Volume: 10, Issue:10
A Bioreductive Prodrug of Cucurbitacin B Significantly Inhibits Tumor Growth in the 4T1 Xenograft Mice Model.
AID1570846Cytotoxicity against human MCF7 cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay2019ACS medicinal chemistry letters, Oct-10, Volume: 10, Issue:10
A Bioreductive Prodrug of Cucurbitacin B Significantly Inhibits Tumor Growth in the 4T1 Xenograft Mice Model.
AID71672Percent of untreated control cell growth evaluated in friend leukemia cells on day 3 at a concentration of 2 mM1981Journal of medicinal chemistry, Sep, Volume: 24, Issue:9
Cyclic urea and thiourea derivatives as inducers of murine erythroleukemia differentiation.
AID71653The degree of erythroid maturation was measured by assessing the proportion of benzidine-positive cells at a concentration of 2 mM1981Journal of medicinal chemistry, Sep, Volume: 24, Issue:9
Cyclic urea and thiourea derivatives as inducers of murine erythroleukemia differentiation.
AID71664Cell growth of friend erythroleukemia cells measured as percentage of control on day 6 at a concentration of 2 mM1981Journal of medicinal chemistry, Sep, Volume: 24, Issue:9
Cyclic urea and thiourea derivatives as inducers of murine erythroleukemia differentiation.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (10)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (10.00)18.7374
1990's0 (0.00)18.2507
2000's4 (40.00)29.6817
2010's5 (50.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.32

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.32 (24.57)
Research Supply Index2.48 (2.92)
Research Growth Index4.80 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.32)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other11 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]