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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:
Assay:
99%
Form:
crystals
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.)
Quality Level
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signalword
Warning
hcodes
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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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
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