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Merck
CN

D86256

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

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About This Item

Linear Formula:
(C2H5)2NC6H4CHO
CAS Number:
Molecular Weight:
177.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-377-4
Beilstein/REAXYS Number:
511102
MDL number:
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Product Name

4-Diethylaminobenzaldehyde, 99%

InChI key

MNFZZNNFORDXSV-UHFFFAOYSA-N

InChI

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

SMILES string

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

assay

99%

form

crystals

bp

174 °C/7 mmHg (lit.)

mp

37-41 °C (lit.)

Quality Level

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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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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
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
Yasufumi Hayashida et al.
Zoological science, 21(5), 541-551 (2004-06-01)
Retinoic acid (RA), the active derivative of vitamin A, is essential for normal embryonic development of vertebrates because both the lack and excess of RA result in developmental malformations. We previously reported that aryl hydrocarbon receptor (AHR) is also required
Ariel B Rydeen et al.
PLoS biology, 14(11), e2000504-e2000504 (2016-11-29)
Although retinoic acid (RA) teratogenicity has been investigated for decades, the mechanisms underlying RA-induced outflow tract (OFT) malformations are not understood. Here, we show zebrafish embryos deficient for Cyp26a1 and Cyp26c1 enzymes, which promote RA degradation, have OFT defects resulting

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