Date published: 2025-9-19

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Salts

Santa Cruz Biotechnology now offers a broad range of salts for use in various applications. Salts, comprising an extensive category of ionic compounds formed by the neutralization reaction between acids and bases, play a pivotal role in scientific research across multiple disciplines. These compounds are essential in chemistry and biochemistry due to their diverse chemical properties and wide range of applications. In analytical chemistry, salts are used as reagents and standards for various qualitative and quantitative analyses. Researchers utilize salts to control ionic strength in solutions, which is crucial for studying reaction kinetics, solubility, and stability of compounds. In materials science, salts are integral in the synthesis of advanced materials, including ceramics, glasses, and semiconductors, where they contribute to the structural and functional properties of these materials. Environmental scientists study salts to understand their impact on soil and water chemistry, examining processes such as salinization and nutrient cycling in ecosystems. Additionally, salts are fundamental in molecular biology and biochemistry, where they are used to prepare buffers that maintain pH and ionic conditions optimal for enzymatic reactions and protein stability. The study of salts also extends to physical chemistry, where they are employed to investigate colligative properties, such as boiling point elevation and freezing point depression, providing insights into molecular interactions and solution dynamics. The broad applications and significance of salts in scientific research underscore their importance in advancing our understanding of chemical processes and enabling technological innovations across various fields. View detailed information on our available salts by clicking on the product name.

Items 31 to 40 of 426 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Phosphatidic Acid, Dioleoyl

108392-02-5sc-201059
10 mg
$250.00
1
(1)

Dioleoyl phosphatidic acid is a unique phospholipid that exhibits amphiphilic properties, allowing it to form stable micelles and lipid bilayers in aqueous environments. Its molecular structure promotes specific interactions with proteins and other lipids, influencing membrane dynamics and cellular signaling pathways. The compound's behavior as a surfactant enhances its role in stabilizing emulsions, while its reactivity can be modulated by changes in pH and ionic strength, affecting its kinetics in biochemical processes.

Tetraethylammonium chloride

56-34-8sc-202834
25 g
$44.00
2
(1)

Tetraethylammonium chloride is a quaternary ammonium salt characterized by its strong ionic interactions, which enhance solubility in polar solvents. Its unique structure facilitates the formation of ion pairs and influences reaction kinetics in various chemical processes. The compound exhibits distinct electrostatic properties, allowing it to act as a phase transfer catalyst. Additionally, its ability to disrupt hydrogen bonding networks in solution can alter the behavior of surrounding molecules, impacting reaction pathways.

Carbenicillin disodium salt

4800-94-6sc-202519
sc-202519A
sc-202519B
250 mg
1 g
5 g
$45.00
$129.00
$306.00
4
(1)

Carbenicillin disodium salt is a unique ionic compound that exhibits strong solvation effects due to its dual sodium ions, enhancing its stability in aqueous environments. Its structure promotes specific interactions with target molecules, influencing reaction dynamics and selectivity. The salt's high degree of dissociation in solution leads to increased ionic strength, which can modulate reaction rates and equilibria. Additionally, its capacity to form complexes with metal ions can alter catalytic pathways, showcasing its versatile reactivity.

Potassium carbonate sesquihydrate

6381-79-9sc-203349
1 kg
$125.00
(0)

Potassium carbonate sesquihydrate is a distinctive crystalline salt characterized by its hygroscopic nature, allowing it to absorb moisture from the environment. This property enhances its solubility in water, facilitating rapid ionization and promoting effective ionic interactions. The presence of water molecules in its structure influences the stability of the compound, while its ability to act as a buffering agent can regulate pH levels in various systems. Its unique lattice arrangement contributes to specific thermal and mechanical properties, impacting its behavior in diverse chemical processes.

Cytosine β-D-arabinofuranoside hydrochloride

69-74-9sc-221454
sc-221454A
25 mg
1 g
$38.00
$160.00
2
(1)

Cytosine β-D-arabinofuranoside hydrochloride is a unique salt that exhibits notable solubility in polar solvents, facilitating swift dissolution and ion dissociation. Its structural conformation allows for specific hydrogen bonding interactions, enhancing its reactivity in biochemical pathways. The compound's chloride ion contributes to its ionic strength, influencing reaction kinetics and stability in solution. Additionally, its crystalline form can affect the rate of dissolution, impacting its behavior in various chemical environments.

Sodium pyrophosphate decahydrate

13472-36-1sc-203404
sc-203404A
sc-203404B
sc-203404C
100 g
500 g
1 kg
2.5 kg
$45.00
$150.00
$242.00
$370.00
(1)

Sodium pyrophosphate decahydrate is a versatile salt characterized by its ability to form chelates with metal ions, enhancing its role in various chemical processes. Its unique layered crystal structure promotes strong ionic interactions, which can influence solubility and reactivity. The compound exhibits buffering capacity, stabilizing pH levels in solution, while its hydration shell plays a crucial role in modulating reaction kinetics. This salt's distinct properties make it a key player in various industrial applications.

Dimethyl-W84 dibromide

402475-33-6sc-202140
5 mg
$92.00
(1)

Dimethyl-W84 dibromide is a distinctive salt known for its strong ionic character and ability to engage in halogen bonding, which can significantly influence molecular interactions. Its unique dipole moments facilitate specific reaction pathways, enhancing nucleophilic attack in organic synthesis. The compound's crystalline form exhibits anisotropic properties, affecting its solubility and reactivity in various solvents. Additionally, its thermal stability allows for controlled decomposition in specific conditions, making it an intriguing subject for further study.

POM 1

12141-67-2sc-203205
sc-203205A
50 g
250 g
$163.00
$433.00
13
(1)

POM 1 is a notable salt characterized by its robust ionic interactions and propensity for forming complex coordination compounds. Its unique electronic structure promotes distinctive reaction kinetics, particularly in nucleophilic substitution reactions. The compound's solubility profile varies significantly with temperature and solvent polarity, influencing its reactivity. Furthermore, POM 1 exhibits interesting electrochemical properties, making it a subject of interest in studies of ionic conductivity and charge transfer mechanisms.

Potassium hexacyanoferrate(III)

13746-66-2sc-203355
sc-203355A
sc-203355B
sc-203355C
sc-203355D
sc-203355E
100 g
250 g
1 kg
2.5 kg
5 kg
10 kg
$42.00
$95.00
$117.00
$229.00
$403.00
$764.00
(1)

Potassium hexacyanoferrate(III) is a fascinating salt known for its intricate lattice structure and ability to form stable complexes with various metal ions. Its unique geometry facilitates strong ligand interactions, enhancing its reactivity in redox processes. The compound demonstrates notable solubility in polar solvents, which affects its dissociation behavior. Additionally, it exhibits distinct colorimetric properties, making it useful in analytical chemistry for detecting specific ions through complex formation.

Polyinosinic acid - polycytidylic acid sodium salt, double-stranded

42424-50-0sc-204854
sc-204854A
10 mg
100 mg
$139.00
$650.00
2
(1)

Polyinosinic acid - polycytidylic acid sodium salt, a double-stranded nucleic acid, exhibits unique structural stability due to its helical conformation, which promotes specific base pairing interactions. This compound is characterized by its ability to form robust hydrogen bonds, influencing its solubility in aqueous environments. Its ionic nature enhances electrostatic interactions, facilitating complex formation with cations. The compound's distinct molecular dynamics contribute to its behavior in biochemical pathways, impacting nucleic acid stability and interactions.