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%
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
Quality Level
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)
National Toxicology Program technical report series, (566)(566), 1-174 (2011-12-01)
Diethylamine is used mainly as a chemical intermediate to produce the corrosion inhibitor N,N-diethylethanolamine and a lesser amount is used to produce pesticides and insect repellants and in rubber processing. Diethylamine was nominated for study by the National Institute of
Doron Yariv et al.
Colloids and surfaces. B, Biointerfaces, 78(2), 185-192 (2010-04-07)
In this paper we examined feasible correlations between the structure of different lyotropic mesophases and transdermal administration of three diclofenac derivatives with varying degrees of kosmotropic or chaotropic properties, solubilized within the mesophases. It was found that the most chaotropic
Clarence M Ongkudon et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 878(28), 2719-2725 (2010-09-03)
Anion exchange monolithic chromatography is increasingly becoming a prominent tool for plasmid DNA purification but no generic protocol is available to purify all types of plasmid DNA. In this work, we established a simple framework and used it to specifically
Jingfeng Chen et al.
Biochimica et biophysica acta, 1807(5), 491-502 (2011-03-17)
Mitochondria-derived oxygen-free radical(s) are important mediators of oxidative cellular injury. It is widely hypothesized that excess NO enhances O(2)(•-) generated by mitochondria under certain pathological conditions. In the mitochondrial electron transport chain, succinate-cytochrome c reductase (SCR) catalyzes the electron transfer
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