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127744

Sigma-Aldrich

Diethylamine hydrochloride

ReagentPlus®, 99%

Synonym(s):

Diethylammonium chloride

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About This Item

Linear Formula:
(C2H5)2NH · HCl
CAS Number:
Molecular Weight:
109.60
Beilstein:
3590084
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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)

SMILES string

Cl.CCNCC

InChI

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

InChI key

HDITUCONWLWUJR-UHFFFAOYSA-N

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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

Signal Word

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 Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Hebeish A and El-Hilw ZH.
Journal of Applied Polymer Science, 67(4) (1998)
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
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.
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
Spencer S Ericksen et al.
The Journal of pharmacology and experimental therapeutics, 342(2), 472-485 (2012-05-17)
In an effort to delineate how specific molecular interactions of dopamine receptor ligand classes vary between D2-like dopamine receptor subtypes, a conserved threonine in transmembrane (TM) helix 7 (Thr7.39), implicated as a key ligand interaction site with biogenic amine G

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