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38960

Sigma-Aldrich

Dimethylamine hydrochloride

purum, ≥98.0% (AT)

Synonym(s):

N,N-Dimethylamine hydrochloride, N-Methylmethanamine hydrochloride, Dimethylammonium chloride

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$147.00

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50 G
$36.70
250 G
$65.60
1 KG
$147.00

About This Item

Linear Formula:
(CH3)2NH · HCl
CAS Number:
Molecular Weight:
81.54
Beilstein/REAXYS Number:
3589311
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

$36.70


Available to ship onApril 30, 2025Details


Request a Bulk Order

grade

purum

Quality Level

assay

≥98.0% (AT)

impurities

≤2% water

mp

170-173 °C (lit.)

solubility

H2O: 0.5 g/10 mL

functional group

amine

SMILES string

Cl[H].CNC

InChI

1S/C2H7N.ClH/c1-3-2;/h3H,1-2H3;1H

Inchi Key

IQDGSYLLQPDQDV-UHFFFAOYSA-N

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Pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Cassandra G F Siler et al.
Journal of the American Chemical Society, 134(30), 12604-12610 (2012-07-10)
A general mechanism for the oxygen-assisted synthesis of amides over metallic gold and silver surfaces has been derived from the study of acetaldehyde and dimethylamine in combination with previous work, allowing detailed comparison of the two surfaces' reactivities. Facile acetylation
Jingyu Gou et al.
Journal of food science, 75(7), M489-M495 (2011-05-04)
The quality properties of semidried squid treated with high-pressure processing (HPP) were investigated during refrigerated storage. The vacuum-packed semidried squid samples were subjected to 500 MPa for 0 min (HPP-0), 5 min (HPP-5), and 10 min (HPP-10) by using a
Jeanne Luh et al.
Environmental science & technology, 46(9), 5085-5092 (2012-03-22)
N-Nitrosodimethylamine (NDMA) formation experiments conducted in phosphate buffer demonstrated that in waters containing monochloramine, the presence of bromide ion enhanced NDMA formation at the relatively high pH values of 8 and 9 after 24 h of reaction time, which was
Francisco G Sánchez et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 83(1), 88-93 (2011-09-17)
The effect of different solvents on the fluorescent properties of 2-(dimethylamine)fluorene (DAF) were studied. In aprotic solvents we detected a strongly emissive intramolecular charge transfer (ICT) state that decayed by intersystem crossing to triplet. In proton-accepting solvents DAF exhibits in
P Andrzejewski et al.
Journal of hazardous materials, 229-230, 340-345 (2012-07-10)
The paper concerns formation of N-nitrosodimethylamine (NDMA) upon ozonation of dimethylamine (DMA) aqueous solutions. According to current hypothesis ozonated DMA is oxidized to N-dimethylhydroxylamine (DMHA), then to N-methylhydroxylamine (MHA) and finally to hydroxylamine (HA). HA subsequently reacts with the remain

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