623-27-8
Chemical Structure
Terephthalaldehyde
- CAS No.: 623-27-8
- Formula:C8H6O2
- Molecular Weight:134.13
IUPAC Name: terephthalaldehyde
InChIKey: KUCOHFSKRZZVRO-UHFFFAOYSA-N
SMILES: O=CC1=CC=C(C=O)C=C1
Biological Activity: Terephthalaldehyde is a crosslinking agent. Terephthalaldehyde forms a crosslinked structure inside the gelatin matrix by forming Schiff base imines with the amino groups of gelatin, thereby constructing a three-dimensional network. Terephthalaldehyde improves the hydrophobicity of the gelatin matrix, delays water vapor penetration and enhances the liquid water resistance of gelatin films. Terephthalaldehyde can be used as a crosslinking agent to prepare crosslinked chitosan hydrogel (CAAT) via ultrasound-induced synthesis. Terephthalaldehyde helps CAAT hydrogels selectively adsorb anionic dyes from aqueous media, including multi-component systems containing cationic dyes. Terephthalaldehyde serves as a starting material for the synthesis of bis-heterocyclic compounds (including bis-thiazole and bis-triazolopyrimidine compounds)[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Terephthalaldehyde | 99.91% | Terephthalaldehyde is a crosslinking agent. Terephthalaldehyde forms a crosslinked structure inside the gelatin matrix by forming Schiff base imines with the amino groups of gelatin, thereby constructing a three-dimensional network. Terephthalaldehyde improves the hydrophobicity of the gelatin matrix, delays water vapor penetration and enhances the liquid water resistance of gelatin films. Terephthalaldehyde can be used as a crosslinking agent to prepare crosslinked chitosan hydrogel (CAAT) via ultrasound-induced synthesis. Terephthalaldehyde helps CAAT hydrogels selectively adsorb anionic dyes from aqueous media, including multi-component systems containing cationic dyes. Terephthalaldehyde serves as a starting material for the synthesis of bis-heterocyclic compounds (including bis-thiazole and bis-triazolopyrimidine compounds). | ||||||||||||||||||||
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4-Bromobenzaldehyde | 99.60% | 4-Bromobenzaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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4-Bromobenzaldehyde-13C6 | 4-Bromobenzaldehyde-13C6 is the 13C labeled 4-Bromobenzaldehyde. | |||||||||||||||||||||
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4-Iodobenzaldehyde | 99.93% | 4-Iodobenzaldehyde is an aromatic halobenzaldehyde derivative and synthetic intermediate. 4-Iodobenzaldehyde is used for the synthesis of various bioactive molecules such as chalcones, heterocycles, receptor antagonists and channel blockers. | ||||||||||||||||||||
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Phthalaldehyde | 99.80% | Phthalaldehyde (Phthaldialdehyde) reacts with proteins containing primary amines and blocked amino-terminal peptides of amino acids. Phthalaldehyde stabilizes bacterial outer membranes and cell walls, increases the optical density of bacterial cell suspensions, and inhibits bacterial lysis induced by ethylenediaminetetraacetic acid and sodium dodecyl sulfate. Phthalaldehyde exhibits bactericidal activity against Gram-negative vegetative bacteria. | ||||||||||||||||||||
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p-Tolualdehyde (Standard) | ≥98% | p-Tolualdehyde (Standard) is the analytical standard of p-Tolualdehyde. This product is intended for research and analytical applications. p-Tolualdehyde is the active small molecule, that could used as drug intermediate. | ||||||||||||||||||||
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4-Aminobenzaldehyde | 99.88% | 4-Aminobenzaldehyde (p-aminobenzaldehyde) is a useful synthetic reagent and monomer that can be used to synthesize monoazo dyes and photocurable ion exchange resins. 4-Aminobenzaldehyde is also a corrosion inhibitor of metals. | ||||||||||||||||||||
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P-Hydroxybenzaldehyde-13C6 | P-Hydroxybenzaldehyde-13C6 is the 13C-labeled p-Hydroxybenzaldehyde (HY-Y0313). p-Hydroxybenzaldehyde is a one of the major components in vanilla aroma, with antagonistic effect on GABAA receptor of the α1β2γ2S subtype at high concentrations. | |||||||||||||||||||||
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4-Fluorobenzaldehyde | 98.23% | 4-Fluorobenzaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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p-Hydroxybenzaldehyde | 99.99% | p-Hydroxybenzaldehyde is a one of the major components in vanilla aroma, with antagonistic effect on GABAA receptor of the α1β2γ2S subtype at high concentrations. | ||||||||||||||||||||
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p-Hydroxybenzaldehyde-13C | p-Hydroxybenzaldehyde-13C is the 13C-labeled p-Hydroxybenzaldehyde. p-Hydroxybenzaldehyde is a one of the major components in Dendrocalamus asper bamboo shoots, with antagonistic effect on GABAA receptor of the α1β2γ2S subtype at high concentrations. | |||||||||||||||||||||
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References
- [1]. Biscarat J, et al. Effect of chemical cross-linking on gelatin membrane solubility with a non-toxic and non-volatile agent: terephthalaldehyde. Int J Biol Macromol. 2015;74:5-11. [Content Brief]
- [2]. Garg M, et al. Terephthalaldehyde as a good crosslinking agent in crosslinked chitosan hydrogel for the selective removal of anionic dyes[J]. New Journal of Chemistry, 2021, 45(11): 4938-4949.
- [3]. Gomha S M, et al. Terephthalaldehyde: An Effecient Key Precursor for Novel Synthesis of Some Interesting Bis‐thiazoles and Bis‐triazolopyrimidinones[J]. Journal of Heterocyclic Chemistry, 2018, 55(3): 750-755.