Skip to Content
Merck
All Photos(2)

Documents

D86256

Sigma-Aldrich

4-Diethylaminobenzaldehyde

99%

Synonym(s):

4-(Diethylamino)benzaldehyde, 4-(N,N-Diethylamine)benzaldehyde, 4-(N,N-Diethylamino)benzaldehyde, 4-(N,N-Diethylphenyl)aldehyde, 4-Formyl-N,N-diethylaniline, N,N-Diethyl-4-formylaniline, N,N-Diethylaminobenzaldehyde, p-(Diethylamino)benzaldehyde, p-(N,N-Diethylamino)benzaldehyde, p-Formyl-N,N-diethylaniline

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(C2H5)2NC6H4CHO
CAS Number:
Molecular Weight:
177.24
Beilstein:
511102
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

crystals

bp

174 °C/7 mmHg (lit.)

mp

37-41 °C (lit.)

SMILES string

[H]C(=O)c1ccc(cc1)N(CC)CC

InChI

1S/C11H15NO/c1-3-12(4-2)11-7-5-10(9-13)6-8-11/h5-9H,3-4H2,1-2H3

InChI key

MNFZZNNFORDXSV-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Xinyi Mu et al.
Journal of cellular physiology, 228(3), 627-639 (2012-08-14)
Meiotic initiation of germ cells at 13.5 dpc (days post-coitus) indicates female sex determination in mice. Recent studies reveal that mesonephroi-derived retinoic acid (RA) is the key signal for induction of meiosis. However, whether the mesonephroi is dispensable for meiosis
P Parameshwara et al.
Annali di chimica, 97(10), 1097-1106 (2007-12-25)
4-(N,N-diethylamino)benzaldehyde thiosemicarbazone(DEABT) is proposed as a sensitive and selective analytical reagent for the spectrophotometric determination of palladium(II). The reagent reacts with palladium (II) in a potassium hydrogen phthalate-hydrochloric acid buffer of pH 3.0, to form a yellow complex. Beer's law
Inhibition of mouse cytosolic aldehyde dehydrogenase by 4-(diethylamino)benzaldehyde.
J E Russo et al.
Biochemical pharmacology, 37(8), 1639-1642 (1988-04-15)
M I Mahmoud et al.
Alcoholism, clinical and experimental research, 17(6), 1223-1227 (1993-12-01)
The compound 4-(diethylamino)benzaldehyde (DEAB) is a potent inhibitor of cytosolic (class 1) aldehyde dehydrogenase (ALDH) in vitro and can overcome cyclophosphamide resistance in murine leukemia cells characterized by their high content of ALDH. In this study, we examined the in
Yu-Chieh Liao et al.
Journal of pharmaceutical and biomedical analysis, 39(3-4), 724-729 (2005-06-14)
Methoxyamine (MX) is a potential new anti-cancer drug. In this paper, a quantitative HPLC-UV method for MX using 4-(diethylamino)benzaldehyde (DEAB) as a derivatizing agent has been developed and validated. The studies showed that MX reacts with DEAB under acidic conditions

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service