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Merck
CN

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%
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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

Application

Diethylamine hydrobromide was used in the synthesis of α-bromovinyltrimethylsilane.

pictograms

Exclamation mark

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)
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
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
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
Nathalie Hasler-Nguyen et al.
BMC research notes, 5, 321-321 (2012-06-23)
Rubbing a topical NSAID (non steroidal anti-inflammatory drug) on the skin may increase local drug permeation, affecting its distribution to the site of pain and inflammation. The present study evaluates this hypothesis, by assessing in vitro the effect on skin

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