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Merck

426458

Dimethylamine solution

40 wt. % in H2O

Synonym(s):

DMA

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About This Item

Linear Formula:
(CH3)2NH
CAS Number:
124-40-3
Molecular Weight:
45.08
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
24866705
MDL number:
MFCD00008288
Beilstein/REAXYS Number:
605257

Key Documents

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Product Name

Dimethylamine solution, 40 wt. % in H2O

InChI

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

SMILES string

CNC

InChI key

ROSDSFDQCJNGOL-UHFFFAOYSA-N

vapor density

1.55 (vs air)

vapor pressure

16.97 psi ( 55 °C)
212 mmHg ( 20 °C)

form

liquid

autoignition temp.

753 °F

concentration

38-42% (with HCl, titration)
40 wt. % in H2O

refractive index

n20/D 1.37

density

0.89 g/mL at 25 °C

functional group

amine

Quality Level

200

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Application

Dimethylamine (DMA) solution can be used:
  • To synthesize Ge7O14.5F2‚[(CH3)2NH2]3(H2O)0.86, a germanate-based porous inclusion complex.
  • To synthesize ethyl 2-dimethylamino-4,6-diarylpyrimidine-5-carboxylates.
  • To convert 5′-bromo-2,2′-bithiophene-5carboxaldehyde to 5′-dimethylamino-2,2′-bithiophene-5-carboxaldehyde.

General description

Dimethylamine is utilized as a building block or reagent in the production of polyurethanes, ion-exchange resins, and dyes.

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

wgk

WGK 1

flash_point_f

60.8 °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
BCCF5520
MKCN5922
SHBG9618V
MKCL0520
BCCB4541

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Polymer-assisted synthesis of ethyl 2-amino-4, 6-diarylpyrimidine-5-carboxylates.
Eynde V, et al.
ARKIVOC (Gainesville, FL, United States), 15, 2003-2003 (2003)
Porous Germanates: Synthesis, Structure, and Inclusion Properties of Ge7O14.5F2.[(CH3)2NH2]3(H2O) 0.86.
Li H, et al.
Journal of the American Chemical Society, 120(33), 8567-8568 (1998)
Ping Yan et al.
The Journal of organic chemistry, 73(17), 6587-6594 (2008-07-31)
There is a growing need for cellular imaging with fluorescent probes that emit at longer wavelengths to minimize the effects of absorption, autofluorescence, and scattering from biological tissue. In this paper a series of new environmentally sensitive hemicyanine dyes featuring
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
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