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Home > Organic Chemistry > Aldehydes (Find 7 items)

Aldehydes

Find our top aldehydes raw materials to improve your cosmetic formulations. If you are exploring the role of aldehydes in perfumes, extraction of cinnamic aldehyde or other related aldehydes, our suppliers provide diverse materials with high quality and competitive prices. Every product is attached to comprehensive CAS NO., property details, and technical data.

Indole-3-carboxaldehyde

(487-89-8)
Pharmaceutical intermediates; starting materials for the synthesis of higher-order indoles, including isoindolo[2,1-a]indoles, aplysinopsins and 4-substituted tetrahydrobenz[cd]indoles

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Imidazole-4-carboxaldehyde

(3034-50-2)
4-Imidazolecarboxaldehyde is a 4-formyl derivative of imidazole used in the preparation of C17,20-lyase inhibitor for the treatemnet of androgen-dependent prostate cancer. 4-Imidazolecarboxaldehyde is also used in the synthesis of other biologically active compounds such as antimalarial drugs.

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Imidazole-2-carboxaldehyde

(10111-08-7)
Used in a study of the imidazole-directed allylation of aldimines.1 Used to study imidazole-directed aldimine allylation reaction.

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Indole-5-carboxaldehyde

(1196-69-6)
Reactant in preparation of curcumin derivatives as anti-proliferative & anti-inflammatory agents 1 Reactant in preparation of analogs of botulinum neurotoxin serotype A protease inhibitors 2 Reactant in stereoselective synthesis of dibenzylideneacetone derivatives as β-amyloid imaging probes 3 Reactant in synthesis of para-para stilbenophanes by McMurry coupling 4 Reactant in stereoselective synthesis of heteroaromatic (E)-α,β-unsaturated ketones from aldehydes 5 Reactant in structure-based drug

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Indole-4-carboxaldehyde

(1074-86-8)
Usually used as reactant in Biginelli reaction,preparation of antitumor agents,intramolecular Friedel-Crafts acylation,preparation of inhibitors of cell division in E. Coli,synthesis of Hantzsch pyridine-containing Schiff bases.

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Indole-7-carboxaldehyde

(1074-88-0)
Used in an efficient synthesis of fused pyrroloquinolinedicarboxylates from acetylenedicarboxylates and triphenylphosphine. 1.reactant for preparation of antiandrogens. 2.reactant for preparation of antiplatelet agent. 3.reactant for preparation of liver

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Indole-6-carboxaldehyde

(1196-70-9)
Reactant in preparation of analogs of botulinum neurotoxin serotype A protease inhibitors 1 Reactant in synthesis of stilbene-based antitumor agents 2 Reactant in acid-catalyzed preparation of aromatic gem-dihalides from aldehydes and acid halides.

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An aldehyde is a compound in which a hydrocarbon group (or hydrogen atom) is connected to an aldehyde group. Aldehydes can be divided into fatty aldehydes and aromatic aldehydes, monoaldehyde and dialdehydes. Aldehydes are mainly strongly reducing, and their oxidizing properties are average. Aldehyde groups are relatively lively and can undergo addition and condensation reactions.

More Information

Aldehyde is an organic compound with the general formula RCHO, where R stands for hydrocarbon group. Aldehydes are composed of a hydrocarbon group (or hydrogen atom) connected to an aldehyde group (-CHO). It contains carbonyl groups in their molecules, with hydrogen atoms directly connected to the carbonyl group. Based on the different hydrocarbon groups, aldehydes can be classified as aromatic aldehydes, fatty aldehydes and so on.

The relevant chemical reactions of aldehydes contain nucleophilic addition reaction and oxidation reaction. They can be obtained by alcohol oxidation, olefin oxidation, alkyne hydration, etc. Besides, Aldehyde compounds have many vital chemical properties and applications, such as participating in various chemical reactions and being important intermediates in the process of organic synthesis.

The application of oxidation of aldehydes

1. Synthesize chemical industrial products, such as methanoic acid

2. Synthesize ketone compounds

3. Used in biology study

Frequently Asked Questions

What are aldehydes and how are they used in the chemical industry?

Aldehydes are organic compounds containing a carbonyl group bonded to at least one hydrogen atom (–CHO). They are widely used as intermediates in the synthesis of pharmaceuticals, fragrances, dyes, and polymers. Common examples include formaldehyde and benzaldehyde. Their reactivity makes them essential building blocks in fine chemical and specialty chemical manufacturing.

What are the key safety considerations when handling aldehydes?

Many aldehydes are volatile, flammable, and potentially toxic or irritant. Key safety measures include using proper personal protective equipment (PPE), ensuring adequate ventilation, and storing them away from heat and oxidizing agents. Some aldehydes, like formaldehyde, are classified as carcinogens, so compliance with OSHA or REACH guidelines is critical for workplace safety and regulatory adherence.

How do I choose a reliable supplier for high-purity aldehydes?

When selecting a supplier for high-purity aldehydes, verify their certifications (e.g., ISO 9001, GMP if applicable), analytical testing capabilities (such as GC or HPLC reports), and consistency in batch quality. A reputable supplier should provide detailed safety data sheets (SDS), traceability documentation, and technical support for applications in research or industrial processes.

What are common applications of aromatic aldehydes like benzaldehyde?

Aromatic aldehydes such as benzaldehyde are primarily used in the production of flavor and fragrance compounds (e.g., cherry or almond flavors), pharmaceutical intermediates (like chloramphenicol), and agrochemicals. They also serve as solvents or precursors in organic synthesis, including the manufacture of dyes and UV stabilizers.

How are aldehydes different from ketones in chemical structure and reactivity?

Both aldehydes and ketones contain a carbonyl group (C=O), but in aldehydes, the carbonyl carbon is bonded to at least one hydrogen atom, whereas in ketones, it is bonded to two carbon atoms. This structural difference makes aldehydes generally more reactive—especially toward oxidation—allowing them to be easily converted to carboxylic acids, while ketones are more resistant to oxidation.

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