310905
Diethylamine hydrobromide
98%
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About This Item
Fórmula lineal:
(C2H5)2NH · HBr
Número de CAS:
Peso molecular:
154.05
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
Quality Level
assay
98%
mp
218-220 °C (lit.)
functional group
amine
SMILES string
Br[H].CCNCC
InChI
1S/C4H11N.BrH/c1-3-5-4-2;/h5H,3-4H2,1-2H3;1H
InChI key
AATGHKSFEUVOPF-UHFFFAOYSA-N
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Categorías relacionadas
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_germany
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)
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
Helmut Görner
The journal of physical chemistry. A, 115(29), 8208-8215 (2011-06-22)
The photoreduction of 6-nitrospiro[2H-1-benzopyran-2,2'-indoline] (N1) and two derivatives (N2 and N3) by diethylamine or triethylamine (TEA) in solution was studied by pulsed and steady-state photolysis. The quantum yield of coloration of the ring-closed Sp form, due to photoinduced ring opening
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
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
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