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126365

Sigma-Aldrich

Dimethylamine hydrochloride

99%

Sinónimos:

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

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About This Item

Fórmula lineal:
(CH3)2NH · HCl
Número de CAS:
506-59-2
Peso molecular:
81.54
Beilstein/REAXYS Number:
3589311
EC Number:
208-046-5
MDL number:
MFCD00012477
UNSPSC Code:
12352100
PubChem Substance ID:
24847723
NACRES:
NA.22

Quality Level

200

assay

99%

form

solid

mp

170-173 °C (lit.)

solubility

H2O: very soluble
alcohol: soluble
diethyl ether: soluble

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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Application

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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Referencia del producto
Descripción
Precios

pictograms

Exclamation mark
GHS07

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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N-demethylation of the antineoplastic agent hexamethylmelamine by rats and man.
J F Worzalla et al.
Cancer research, 33(11), 2810-2815 (1973-11-01)
Mark E Erupe et al.
Journal of chromatography. A, 1217(13), 2070-2073 (2010-02-26)
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
Mojca Seručnik et al.
The journal of physical chemistry. B, 122(21), 5381-5388 (2018-01-26)
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
Adam F Nugraha et al.
Polymers, 12(7) (2020-07-24)
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
Patrick L Feng et al.
Dalton transactions (Cambridge, England : 2003), 41(29), 8869-8877 (2012-06-19)
One of the ongoing goals in the field of porous materials is the design and synthesis of materials that possess chemical structures amenable for use in sensing applications. We describe the preparation, luminescence characteristics, and environmental sensing properties of variants
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