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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

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About This Item

Linear Formula:
(C2H5)2NC6H4CHO
CAS Number:
120-21-8
Molecular Weight:
177.24
Beilstein:
511102
EC Number:
204-377-4
MDL number:
MFCD00003382
UNSPSC Code:
12352100
PubChem Substance ID:
24894106
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

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H312,H315,H319,H335

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCL1306
MKCB6376
MKBQ7330V
MKBJ8393V
MKBG2492V

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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
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
Inhibition of mouse cytosolic aldehyde dehydrogenase by 4-(diethylamino)benzaldehyde.
J E Russo et al.
Biochemical pharmacology, 37(8), 1639-1642 (1988-04-15)
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
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
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