Date published: 2025-10-18

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Ketones

Santa Cruz Biotechnology now offers a broad range of ketones for use in various applications. Ketones, characterized by a carbonyl group bonded to two carbon atoms, are a versatile and widely studied class of organic compounds that play a crucial role in numerous scientific fields. In organic chemistry, ketones are fundamental intermediates in a variety of synthetic pathways, enabling the creation of complex molecules through reactions such as aldol condensations, reductions, and Grignard additions. Their reactivity and stability make them ideal for use in the development of polymers, resins, and other industrial chemicals. In the realm of environmental science, ketones are utilized in studies of atmospheric chemistry and pollutant degradation, helping researchers understand and mitigate environmental impacts. Additionally, ketones serve as important solvents and reagents in analytical chemistry, where they facilitate the separation, identification, and quantification of various compounds. In biochemistry, ketones are investigated for their roles in metabolic pathways, particularly in the context of energy production and storage. Their distinctive chemical properties also make ketones valuable in materials science for the design of advanced materials with tailored functionalities. The widespread applicability and essential nature of ketones in scientific research underscore their importance in driving innovation and expanding our understanding of chemical processes. View detailed information on our available ketones by clicking on the product name.

Items 161 to 170 of 214 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

2-Bromo-1-(4-cyclohexylphenyl)ethanone

99433-28-0sc-282950
sc-282950A
1 g
5 g
$400.00
$1185.00
(0)

2-Bromo-1-(4-cyclohexylphenyl)ethanone, as a ketone, showcases intriguing reactivity stemming from its bromine substituent, which introduces significant steric hindrance and alters electronic distribution. This compound engages in selective nucleophilic attacks, leading to the formation of various adducts. Its bulky cyclohexyl group enhances conformational rigidity, influencing reaction pathways and kinetics. The compound's polar characteristics also play a crucial role in solubility and interaction with solvents, affecting its reactivity in diverse chemical contexts.

4-Oxo-2-nonenal

103560-62-9sc-202020
sc-202020A
1 mg
5 mg
$150.00
$720.00
(0)

4-Oxo-2-nonenal, as a ketone, exhibits notable reactivity due to its conjugated carbonyl group, which enhances electrophilicity and facilitates Michael addition reactions. The presence of the unsaturated chain allows for unique interactions with nucleophiles, promoting diverse reaction pathways. Its structural features contribute to distinct physical properties, such as increased volatility and reactivity with various functional groups, influencing its behavior in complex chemical environments.

(R)-(+)-HA-966

123931-04-4sc-361303
5 mg
$95.00
(0)

(R)-(+)-HA-966, as a ketone, showcases intriguing stereochemical properties that influence its reactivity and interaction with other molecules. The chiral center enhances its selectivity in reactions, allowing for specific pathways in synthesis. Its carbonyl group participates in hydrogen bonding, affecting solubility and reactivity with nucleophiles. Additionally, the compound's unique spatial arrangement can lead to distinct kinetic profiles in reactions, making it a subject of interest in mechanistic studies.

YM 976

191219-80-4sc-204411
sc-204411A
10 mg
50 mg
$207.00
$825.00
(0)

YM 976, classified as a ketone, exhibits notable electronic properties due to its conjugated system, which enhances its reactivity in electrophilic addition reactions. The presence of the carbonyl group allows for significant dipole interactions, influencing its solubility in various solvents. Its unique steric configuration can lead to selective reactivity, facilitating specific pathways in organic transformations. Furthermore, the compound's kinetic behavior is characterized by rapid reaction rates, making it a compelling subject for studies on reaction mechanisms.

NBI-31772

374620-70-9sc-222047A
sc-222047
sc-222047B
sc-222047C
1 mg
5 mg
10 mg
25 mg
$39.00
$162.00
$267.00
$573.00
(0)

NBI-31772, a ketone, showcases intriguing photophysical properties, particularly in its ability to engage in intramolecular hydrogen bonding, which stabilizes its structure and influences its reactivity. The compound's unique spatial arrangement allows for selective interactions with nucleophiles, promoting distinct reaction pathways. Additionally, its polar nature enhances solvation dynamics, affecting its behavior in various chemical environments and contributing to its kinetic profile in reactions.

FKGK 11

1071000-98-0sc-223989
sc-223989A
500 µg
1 mg
$54.00
$136.00
(0)

FKGK 11, classified as a ketone, exhibits remarkable electronic properties due to its conjugated system, which facilitates efficient charge transfer. This compound demonstrates a propensity for forming stable complexes with metal ions, influencing its reactivity and selectivity in catalytic processes. Its unique steric configuration allows for specific interactions with electrophiles, leading to diverse reaction mechanisms. Furthermore, the compound's moderate polarity enhances its solubility in various organic solvents, impacting its behavior in synthetic applications.

Mesityl oxide

141-79-7sc-250308
100 g
$40.00
(1)

Mesityl oxide, a ketone, features a branched structure that contributes to its unique reactivity profile. Its ability to engage in enolization allows for dynamic equilibrium between keto and enol forms, influencing reaction pathways. The compound's steric hindrance affects its interaction with nucleophiles, leading to selective reactions. Additionally, its moderate volatility and distinct odor can impact its behavior in various chemical environments, making it an interesting subject for study in organic synthesis.

Formononetin

485-72-3sc-202614
5 mg
$122.00
2
(1)

Formononetin, a naturally occurring ketone, exhibits intriguing molecular interactions due to its phenolic structure. This compound can participate in hydrogen bonding, enhancing its solubility in polar solvents. Its reactivity is influenced by the presence of electron-donating groups, which can stabilize transition states during reactions. Furthermore, Formononetin's ability to undergo oxidation and reduction reactions highlights its versatility in organic transformations, making it a subject of interest in chemical research.

2-Chlorocyclohexanone

822-87-7sc-237997
sc-237997A
5 g
25 g
$18.00
$88.00
(0)

2-Chlorocyclohexanone is a unique ketone characterized by its chlorinated cyclohexane ring, which introduces distinct steric and electronic effects. The presence of the chlorine atom enhances electrophilicity, facilitating nucleophilic attack in various reactions. Its ring structure allows for conformational flexibility, influencing reaction pathways and kinetics. Additionally, this compound can engage in dipole-dipole interactions, affecting solubility and reactivity in diverse chemical environments.

1,4-Bis(acryloyl)piperazine

6342-17-2sc-203424
sc-203424A
5 g
10 g
$150.00
$260.00
(0)

1,4-Bis(acryloyl)piperazine is a distinctive compound featuring dual acrylamide functionalities that promote unique polymerization behavior. Its piperazine ring contributes to enhanced hydrogen bonding and dipole interactions, influencing reactivity and stability. The acrylate groups facilitate rapid radical polymerization, allowing for tailored material properties. This compound's ability to form cross-linked networks enhances mechanical strength and thermal stability, making it suitable for diverse applications in polymer chemistry.