38950
Dimethylamine solution
purum, 33% in absolute ethanol (~5.6 M)
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Synonym(s):
N,N-Dimethylamine
Linear Formula:
(CH3)2NH
CAS Number:
Molecular Weight:
45.08
Beilstein:
605257
MDL number:
UNSPSC Code:
41116105
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
purum
Quality Level
form
liquid
concentration
32-34% (titration)
33% in absolute ethanol (~5.6 M)
density
0.76 g/cm3
SMILES string
CNC
InChI
1S/C2H7N/c1-3-2/h3H,1-2H3
InChI key
ROSDSFDQCJNGOL-UHFFFAOYSA-N
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General description
Dimethylamine (DMA) is a versatile organic compound that is commonly used in organic synthesis as a reagent and building block for various reactions. It is also used as a base in several reactions such as the Mannich reaction and Michael addition.
Application
Dimethylamine solution (33% in absolute ethanol) can be used in a sialic acid ethyl esterification reaction. It is also used as a reagent in the Pd-catalyzed C-N bond-forming cross-coupling reactions.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 1
Flash Point(F)
3.2 °F
Flash Point(C)
-16 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
监管及禁止进口产品
Certificates of Analysis (COA)
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C Mulder et al.
Journal of neural transmission (Vienna, Austria : 1996), 109(9), 1203-1208 (2002-08-31)
Nitric oxide (NO) may play a role in the pathophysiology of Alzheimer's disease (AD). Asymmetric dimethylarginine (ADMA), an endogenous inhibitor of NO synthase, is involved in regulation of NO production. Recently it has been reported that dimethylarginine dimethylaminohydrolase, an enzyme
L Lee et al.
Cancer research, 41(10), 3992-3994 (1981-10-01)
Using a method for nitrosamine analysis that gives high recovery values and that is free from artifactual synthesis of nitrosamines, we have shown that human feces do not contain volatile nitrosamines (detection limit, 0.1 to 0.5 microgram/kg). We also showed
Gerhild Zauner et al.
Biochimica et biophysica acta, 1820(9), 1420-1428 (2011-08-02)
Analysis of protein glycosylation is an important first step towards establishing the functions of glycans in health and disease. In contrast to N-glycans which are generally enzymatically released for analysis, there is no corresponding enzyme for O-glycan liberation. Therefore, O-glycans
George Nicholson et al.
PLoS genetics, 7(9), e1002270-e1002270 (2011-09-21)
We have performed a metabolite quantitative trait locus (mQTL) study of the (1)H nuclear magnetic resonance spectroscopy ((1)H NMR) metabolome in humans, building on recent targeted knowledge of genetic drivers of metabolic regulation. Urine and plasma samples were collected from
Meric Selbes et al.
Water research, 47(2), 945-953 (2012-12-15)
N-nitrosodimethylamine (NDMA), a probable human carcinogen, is a disinfection by-product that has been detected in chloraminated and chlorinated drinking waters and wastewaters. Formation mechanisms and precursors of NDMA are still not well understood. The main objectives of this study were
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