Date published: 2025-9-30

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Aldehydes 02

Santa Cruz Biotechnology now offers a broad range of aldehydes for use in various applications. Aldehydes, characterized by the presence of a carbonyl group (C=O) with a hydrogen atom attached to the carbon atom, are highly reactive organic compounds widely utilized in both organic and inorganic chemistry. Their reactivity stems from the electrophilic nature of the carbonyl carbon, making them pivotal intermediates in numerous chemical reactions, including nucleophilic addition, oxidation, and condensation reactions. In scientific research, aldehydes are essential for the synthesis of a diverse array of chemical compounds, such as alcohols, acids, and polymers. They serve as key building blocks in organic synthesis, enabling the construction of complex molecules and the development of new synthetic methodologies. In biochemical research, aldehydes are used to study metabolic pathways, particularly those involving carbohydrate metabolism, as well as in the investigation of enzyme-catalyzed reactions. Additionally, aldehydes play a crucial role in materials science, where they are used to modify and cross-link polymers, enhancing their mechanical properties and durability. Their ability to form Schiff bases with amines also makes them valuable in the design of sensors and detection systems. Environmental scientists utilize aldehydes to study atmospheric chemistry and pollutant formation, as well as in the analysis of natural products and their degradation pathways. By offering a diverse selection of aldehydes, Santa Cruz Biotechnology supports a wide range of scientific endeavors, enabling researchers to select the appropriate aldehyde for their specific experimental needs. This extensive range of aldehydes facilitates innovation and discovery across multiple scientific disciplines, including chemistry, biology, and materials science. View detailed information on our available aldehydes by clicking on the product name.

Items 301 to 310 of 500 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

trans-2-Octenal

2548-87-0sc-237168
5 g
$49.00
(0)

trans-2-Octenal is a cause of defects for locomotion in green fluorescent protein (GFP)

4-Dimethylamino-1-naphthaldehyde

1971-81-9sc-226617
1 g
$153.00
(0)

4-Dimethylamino-1-naphthaldehyde is a napthalene compound

3-(Methylthio)propionaldehyde

3268-49-3sc-231383
5 ml
$56.00
(0)

3-(Methylthio)propionaldehyde is the major product of chemical methionine conversion via Strecker degradation in food

3,5-Diiodosalicylaldehyde

2631-77-8sc-232110
5 g
$30.00
(0)

3,5-Diiodosalicylaldehyde is used to synthesize new Schiff bases

2-Methoxycinnamaldehyde, predominantly trans

1504-74-1sc-230476A
sc-230476
sc-230476B
sc-230476C
1 g
5 g
25 g
100 g
$32.00
$63.00
$150.00
$410.00
(0)

2-Methoxycinnamaldehyde, predominantly trans is A Cinnamomum cassia component

2,3,5-Trichlorobenzaldehyde

56961-75-2sc-230889
5 g
$92.00
(0)

2,3,5-Trichlorobenzaldehyde is a component in the synthesis of α-keto amide

2,3,6-Trichlorobenzaldehyde

4659-47-6sc-230905
5 g
$25.00
(0)

trans-2,cis-6-Nonadienal

557-48-2sc-237179
1 g
$40.00
(0)

2-Methyl-2-pentenal

623-36-9sc-230507
25 g
$31.00
(0)

2-Methyl-2-pentenal is hydrodeoxygenation and hydrogenation of this product on supported platinum, palladium and copper catalysts has been reported

5-Nitro-2-thiophenecarboxaldehyde

4521-33-9sc-233424
5 g
$73.00
(0)

5-Nitro-2-thiophenecarboxaldehyde is a useful chemical for protoemics research as well as the synthesis of 2,3-dihydro-2-(5-nitro-2-thienyl) quinazolin-4-(1H)-ones1 and various novel oxime ether derivatives which are anti-protozoan agents