310905
Diethylamine hydrobromide
98%
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About This Item
Linear Formula:
(C2H5)2NH · HBr
CAS Number:
Molecular Weight:
154.05
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
228-466-2
MDL number:
Assay:
98%
Quality Level
InChI key
AATGHKSFEUVOPF-UHFFFAOYSA-N
InChI
1S/C4H11N.BrH/c1-3-5-4-2;/h5H,3-4H2,1-2H3;1H
SMILES string
Br[H].CCNCC
assay
98%
mp
218-220 °C (lit.)
functional group
amine
Related Categories
Application
Diethylamine hydrobromide was used in the synthesis of α-bromovinyltrimethylsilane.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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SYNTHESES AND POLYMERIZATION OF α-TRIMETHYLSILYL ACRYLIC MONOMERS.
Canadian Journal of Chemistry, 41(12), 2977- 2982 (1963)
Zhao Chunfang et al.
Journal of chromatographic science, 48(8), 685-689 (2010-09-08)
The thin-layer chromatography (TLC) combined with high-performance liquid chromatography (HPLC) has been proved to be a quick and valid method to detect the intermediates and the end-product created during the chemosynthesis process of vinorelbine (VB). This paper gives a detailed
V M Gun'ko et al.
Journal of colloid and interface science, 348(2), 546-558 (2010-07-14)
Adsorption of low-molecular adsorbates (nonpolar hexane, nitrogen, weakly polar acetonitrile, and polar diethylamine, triethylamine, and water) onto individual (silica, alumina, titania), binary (silica/alumina (SA), silica/titania (ST)), and ternary (alumina/silica/titania, AST) fumed oxides was studied to analyse the effects of morphology
Jennifer C Irvine et al.
Antioxidants & redox signaling, 14(9), 1615-1624 (2010-09-21)
Nitroxyl (HNO) displays distinct pharmacology to its redox congener nitric oxide (NO(•)) with therapeutic potential in the treatment of heart failure. It remains unknown if HNO donors are resistant to tolerance development following chronic in vivo administration. Wistar-Kyoto rats received
Junzo Hirano et al.
Journal of fluorescence, 20(2), 615-624 (2010-01-29)
A novel fluorescence enhancement-type derivatizing reagent for amino compounds, 6,7-difluoro-1,4-dihydro-1-methyl-4-oxo-3-quinolinecarboxylic acid (FMQC), was developed. FMQC reacts with aliphatic primary amino compounds to afford strong fluorescent derivatives having high photo-and thermo-stabilities. The FMQC derivatives of amino compounds showed 12-159 times higher
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