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Merck

38950

Dimethylamine solution

purum, 33% in absolute ethanol (~5.6 M)

Synonym(s):

N,N-Dimethylamine

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About This Item

Linear Formula:
(CH3)2NH
CAS Number:
124-40-3
Molecular Weight:
45.08
UNSPSC Code:
41116105
NACRES:
NA.22
PubChem Substance ID:
329755808
MDL number:
MFCD00008288
Beilstein/REAXYS Number:
605257
Concentration:
32-34% (titration), 33% in absolute ethanol (~5.6 M)
Form:
liquid

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InChI

1S/C2H7N/c1-3-2/h3H,1-2H3

SMILES string

CNC

InChI key

ROSDSFDQCJNGOL-UHFFFAOYSA-N

grade

purum

form

liquid

concentration

32-34% (titration), 33% in absolute ethanol (~5.6 M)

density

0.76 g/cm3

functional group

amine

Quality Level

200

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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.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

flash_point_f

3.2 °F - closed cup

flash_point_c

-16 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM6240
BCCH3067
BCCG3855
BCCD1390
BCBL6317V

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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
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
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
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
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
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