Skip to Content
Merck

38960

Dimethylamine hydrochloride

purum, ≥98.0% (AT)

Synonym(s):

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

Sign In to View Organizational & Contract Pricing.

Select a Size

All Photos(1)

About This Item

Linear Formula:
(CH3)2NH · HCl
CAS Number:
506-59-2
Molecular Weight:
81.54
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329755811
EC Number:
208-046-5
Beilstein/REAXYS Number:
3589311
MDL number:
MFCD00012477

Product Name

Dimethylamine hydrochloride, purum, ≥98.0% (AT)

InChI key

IQDGSYLLQPDQDV-UHFFFAOYSA-N

InChI

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

SMILES string

Cl[H].CNC

grade

purum

assay

≥98.0% (AT)

impurities

≤2% water

mp

170-173 °C (lit.)

solubility

H2O: 0.5 g/10 mL

functional group

amine

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCN8469
BCCK7776
BCCH6118
BCCF7065
BCCF1252

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
M L Guzmán et al.
Molecular pharmaceutics, 9(9), 2424-2433 (2012-07-20)
Therapeutic agents containing phosphate groups in their molecules have increasing therapeutic impact. The object of this study was to characterize the cationic polyelectrolyte Eudragit E100 (EuE100) as a carrier for drugs containing phosphate groups, using dexamethasone phosphate (DP) as a
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
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service