100-10-7
100-10-7
Chemical Structure
p-Dimethylaminobenzaldehyde
Synonym(s): 4-Dimethylaminobenzaldehyde
- CAS 番号: 100-10-7
- Formula:C9H11NO
- Molecular Weight:149.19
IUPAC Name: 4-(dimethylamino)benzaldehyde
InChIKey: BGNGWHSBYQYVRX-UHFFFAOYSA-N
SMILES: O=CC1=CC=C(N(C)C)C=C1
Biological Activity: p-Dimethylaminobenzaldehyde (4-Dimethylaminobenzaldehyde) can be used as a chromogenic reagent or as an absorbent agent for heavy metal ions[1][2].
| 製品番号 | 製品名 | 純度 | 製品説明 | Pricing | |||||||||||||||||||
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p-Dimethylaminobenzaldehyde | 99.88% | p-Dimethylaminobenzaldehyde (4-Dimethylaminobenzaldehyde) can be used as a chromogenic reagent or as an absorbent agent for heavy metal ions. | ||||||||||||||||||||
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p-Dimethylaminobenzaldehyde (Standard) | ≥98% | p-Dimethylaminobenzaldehyde (Standard) is the analytical standard of p-Dimethylaminobenzaldehyde. This product is intended for research and analytical applications. p-Dimethylaminobenzaldehyde (4-Dimethylaminobenzaldehyde) can be used as a chromogenic reagent or as an absorbent agent for heavy metal ions. | ||||||||||||||||||||
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P-Dimethylaminobenzaldehyde-d11 | P-Dimethylaminobenzaldehyde-d11 (4-Dimethylaminobenzaldehyde-d11) is the deuterium labeled P-Dimethylaminobenzaldehyde. | |||||||||||||||||||||
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4-(Dimethylamino)phenol (Standard) | ≥98% | 4-(Dimethylamino)phenol (Standard) is the analytical standard of 4-(Dimethylamino)phenol. This product is intended for research and analytical applications. 4-(Dimethylamino)phenol is a potent cyanide antidote. 4-(Dimethylamino)phenol increases the extracellular lactate dehydrogenase (LDH) without markedly affecting gluconeogenesis. 4-(Dimethylamino)phenol cannot decreases the ATP content until the membrane becomes permeable to LDH. 4-(Dimethylamino)phenol’s toxicity is related to its reaction with glutathione and formation of covalent complexes, leading to impaired cellular function. | ||||||||||||||||||||
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p-Tolualdehyde | 99.10% | p-Tolualdehyde is the active small molecule, that could used as drug intermediate. | ||||||||||||||||||||
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3-(4-(Dimethylamino)phenyl)acrylic acid | 3-(4-(Dimethylamino)phenyl)acrylic acid is a Alkaloids product that can be isolated from the barks of Cinnamomum cassia Presl. | |||||||||||||||||||||
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4-Diethylaminobenzaldehyde (Standard) | ≥98% | 4-Diethylaminobenzaldehyde is a reversible aldehyde dehydrogenases (ALDHs) inhibitor, with a Ki of 4 nM for ALDH1. 4-Diethylaminobenzaldehyde displays potent anti-androgenic effect (IC50= 1.71μM). | ||||||||||||||||||||
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4-(Dimethylamino)cinnamaldehyde | 99.89% | 4-(Dimethylamino) cinnamaldehyde is a staining agent that reacts with flavan-3-ols and Proanthocyanidins (HY-N0794) bearing meta-dihydroxyl or trihydroxyl phenol structures to form a green chromophore. In acidic media, 4-(Dimethylamino) cinnamaldehyde undergoes a condensation reaction with aromatic primary amines to produce colored and stable quinoid protonated Schiff base salts. 4-(Dimethylamino) cinnamaldehyde can be used to determine indole products of apotryptophanase and tryptophanase, as well as for the detection and analysis of Proanthocyanidins, with the absorbance detection wavelength of the calibration curve set at 640 nm. | ||||||||||||||||||||
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N,N,N′,N′-Tetramethyl-p-phenylenediamine | 99.96% | N,N,N′,N′-Tetramethyl-p-phenylenediamine is an electron-donating aromatic diamine with a low ionization potential. N,N,N′,N′-Tetramethyl-p-phenylenediamine is a classic electron donor model compound for photochemical electron transfer studies. | ||||||||||||||||||||
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4-(Dimethylamino)phenol hydrochloride | 4-(Dimethylamino)phenol hydrochloride is a potent cyanide antidote. 4-(Dimethylamino)phenol hydrochloride binds to hemoglobin, and form methemoglobin. 4-(Dimethylamino)phenol hydrochloride can be used in cyanide poisoning research. | |||||||||||||||||||||
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4-Methoxybenzaldehyde (Standard) | ≥98% | 4-Methoxybenzaldehyde (Standard) is the analytical standard of 4-Methoxybenzaldehyde. This product is intended for research and analytical applications. 4-Methoxybenzaldehyde (p-anisaldehyde) is a fragrant phenolic compound. 4-Methoxybenzaldehyde has been found in many plant species including horseradish, anise, star anise. 4-Methoxybenzaldehyde is a possible neurotoxicant and it has shown effects that include mortality, attractancy, and interference with host seeking . | ||||||||||||||||||||
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Cuminaldehyde | 99.32% | Cuminaldehyde is the main component of Cuminum cyminum and has multiple biological activities, including anti-inflammatory, anti-cancer, anti-diabetic, anti-injury, anti-neuropathy and antibacterial effects. Cuminaldehyde is an inhibitor of aldose reductase (IC50= 0.00085 mg/mL), α-glucosidase (IC50=0.5 mg/mL) and lipoxygenase (IC50=1370 μM). Cuminaldehyde also inhibits the fibrillation of α-synuclein and prevents its aggregation. Cuminaldehyde has potential application value in the research of neurodegenerative diseases, cancer, diabetes and neuropathic pain diseases. | ||||||||||||||||||||
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References
- [1]. Cline R E, et al., Investigation of color reaction between p-dimethylaminobenzaldehyde and urea or ureido acids[J]. Analytical Chemistry, 1956, 28(1): 47-52.
- [2]. Cui Y, et al. Chemically modified silica gel with p-dimethylaminobenzaldehyde for selective solid-phase extraction and preconcentration of Cr (III), Cu (II), Ni (II), Pb (II) and Zn (II) by ICP-OES[J]. Microchemical Journal, 2007, 87(1): 20-26.
