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Merck

127744

Diethylamine hydrochloride

ReagentPlus®, 99%

Synonym(s):

Diethylammonium chloride

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About This Item

Linear Formula:
(C2H5)2NH · HCl
CAS Number:
660-68-4
Molecular Weight:
109.60
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847795
EC Number:
211-541-9
Beilstein/REAXYS Number:
3590084
MDL number:
MFCD00012499
Assay:
99%
Form:
solid

Key Documents

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Product Name

Diethylamine hydrochloride, ReagentPlus®, 99%

InChI key

HDITUCONWLWUJR-UHFFFAOYSA-N

InChI

1S/C4H11N.ClH/c1-3-5-4-2;/h5H,3-4H2,1-2H3;1H

SMILES string

Cl.CCNCC

product line

ReagentPlus®

assay

99%

form

solid

mp

227-230 °C (lit.)

solubility

H2O: soluble 50 mg/mL, clear, colorless
H2O: soluble, clear, colorless (50 mg/mL)

functional group

amine

Quality Level

100

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Related Categories

Application

Diethylamine hydrochloride has been used in the synthesis of diethylaminoethyl (DEAE) cottons by reacting it with cotton cellulose in the presence of sodium hydroxide.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB6010
SDBB6009
SDBB4483
SDBB3301
STBL3725

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Hebeish A and El-Hilw ZH.
Journal of Applied Polymer Science, 67(4) (1998)
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
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
Dorotea Micieli et al.
Journal of colloid and interface science, 360(2), 359-369 (2011-05-24)
Anti-inflammatory drugs represent a potential new strategy for the treatment of Alzheimer's disease (AD). The ability to cross the blood-brain barrier and to reach brain tissues is a critical point for these drugs and is strictly related to their lipophilicity.
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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