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310905

Sigma-Aldrich

Diethylamine hydrobromide

98%

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About This Item

Fórmula lineal:
(C2H5)2NH · HBr
Número de CAS:
6274-12-0
Peso molecular:
154.05
EC Number:
228-466-2
MDL number:
MFCD00012498
UNSPSC Code:
12352100
PubChem Substance ID:
24858825
NACRES:
NA.22

assay

98%

mp

218-220 °C (lit.)

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.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

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)
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
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
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