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About This Item
Linear Formula:
(CH3)2NH · HCl
CAS Number:
Molecular Weight:
81.54
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-046-5
Beilstein/REAXYS Number:
3589311
MDL number:
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
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Related Categories
signalword
Warning
hcodes
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
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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
Time resolved spectroscopy of 2-(dimethylamine)fluorene. Solvent effects and photophysical behavior.
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
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