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126365

Sigma-Aldrich

Dimethylamin -hydrochlorid

99%

Synonym(e):

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

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About This Item

Lineare Formel:
(CH3)2NH · HCl
CAS-Nummer:
506-59-2
Molekulargewicht:
81.54
Beilstein:
3589311
EG-Nummer:
208-046-5
MDL-Nummer:
MFCD00012477
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24847723
NACRES:
NA.22

Qualitätsniveau

200

Assay

99%

Form

solid

mp (Schmelzpunkt)

170-173 °C (lit.)

Löslichkeit

H2O: very soluble
alcohol: soluble
diethyl ether: soluble

SMILES String

Cl[H].CNC

InChI

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

InChIKey

IQDGSYLLQPDQDV-UHFFFAOYSA-N

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Anwendung

Dimethylamine hydrochloride has been used in the preparation of hexamethylmelamine-methyl-14C. It has also been used to prepare the standard solution of methylamine (MA), dimethylamine (DMA), trimethylamine (TMA), and trimethylamine-N-oxide (TMAO) while determing methylamines and trimethylamine-N-oxide in particulate matter.

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Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Sigma-Aldrich

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N-demethylation of the antineoplastic agent hexamethylmelamine by rats and man.
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Cancer research, 33(11), 2810-2815 (1973-11-01)
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An ion chromatography method with non-suppressed conductivity detection was developed for the simultaneous determination of methylamines (methylamine, dimethylamine, trimethylamine) and trimethylamine-N-oxide in particulate matter air samples. The analytes were well separated by means of cation-exchange chromatography using a 3 mM
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Complexes of polycations and DNA, also known as polyplexes, have been extensively studied in the past decade, as potential gene delivery systems. Their stability depends strongly on the characteristics of the polycations, as well as the nature of the added
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Several methods to synthesize poly(phenylene) block copolymers through the nickel coupling reaction were attempted to reduce the use of expensive nickel catalysts in polymerization. The model reaction for poly(phenylene) having different types of dichlorobenzene derivative monomers illustrated the potential use
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