Date published: 2025-10-20

1-800-457-3801

SCBT Portrait Logo
Seach Input

Zinc Probes

Santa Cruz Biotechnology now offers a broad range of Zinc Probes for use in various applications. Zinc probes are specialized chemical tools designed to detect and measure the presence and concentration of zinc ions, which are crucial for numerous biological and chemical processes. These probes are essential in the field of biochemistry for studying zinc's role in enzymatic functions and its importance in cellular signaling pathways. Zinc's involvement in protein synthesis, gene expression, and metabolic processes makes these probes valuable for research in molecular biology and genetics, providing insights into the fundamental mechanisms of life at the cellular level. In environmental science, zinc probes are utilized to monitor and analyze the contamination of ecosystems by heavy metals, aiding in environmental protection efforts. Furthermore, these probes are crucial in materials science, where they help in the study of zinc-containing materials, including batteries and metal alloys, to improve their properties and efficiency. The application of zinc probes in non-invasive imaging techniques also enhances the study of zinc's distribution and dynamics within live organisms, offering significant benefits to fields such as plant science and microbiology. The ability of these probes to provide specific and quantifiable data about zinc ion concentrations makes them indispensable tools in advancing scientific research across various disciplines. View detailed information on our available Zinc Probes by clicking on the product name.

Items 1 to 10 of 11 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Bromo-PAPS

679787-08-7sc-252254
100 mg
$160.00
(0)

5-Bromo-PAPS is a notable acid halide characterized by its strong electrophilic nature, which promotes rapid interactions with nucleophiles. Its bromine substituent enhances reactivity through unique molecular interactions, allowing for efficient acylation processes. The compound's distinct steric properties facilitate selective reactions, leading to the formation of various derivatives. Additionally, its solubility in polar solvents aids in accelerating reaction kinetics, making it a versatile participant in synthetic chemistry.

TPEN

16858-02-9sc-200131
100 mg
$127.00
10
(3)

TPEN is a chelating agent that exhibits a strong affinity for zinc ions, forming stable complexes through multiple coordination sites. Its unique structure allows for selective binding, influencing zinc's bioavailability and reactivity in various biochemical pathways. The compound's ability to modulate zinc's role in enzymatic processes highlights its significance in metal ion interactions. Furthermore, TPEN's solubility in organic solvents enhances its utility in diverse chemical environments.

ZnAF-2 tetrahydrochloride

sc-222429
1 mg
$487.00
(0)

ZnAF-2 tetrahydrochloride is a highly reactive zinc compound characterized by its ability to form robust coordination complexes with various ligands. Its tetrahedral geometry facilitates unique molecular interactions, promoting rapid reaction kinetics in metal exchange processes. The compound's strong Lewis acidity enhances its reactivity, allowing it to participate in diverse catalytic pathways. Additionally, its solubility in polar solvents broadens its applicability in synthetic chemistry, enabling intricate reaction mechanisms.

ZnAF-2F

443302-09-8sc-216075
sc-216075A
sc-216075B
1 mg
5 mg
25 mg
$172.00
$660.00
$2250.00
1
(0)

ZnAF-2F is a distinctive zinc-based compound known for its exceptional ability to engage in ligand exchange reactions due to its unique electronic structure. The compound exhibits a pronounced tendency to stabilize transition states, which accelerates reaction rates in coordination chemistry. Its high affinity for electron-rich species allows for the formation of stable adducts, while its specific steric properties influence selectivity in reactions. This versatility makes it a key player in various synthetic pathways.

Calcein Blue

54375-47-2sc-214650
sc-214650A
1 g
10 g
$67.00
$362.00
(0)

Calcein Blue is a notable zinc chelator characterized by its strong fluorescence properties, which are influenced by its coordination with zinc ions. This compound exhibits unique binding dynamics, forming stable complexes that enhance its photophysical behavior. The interaction with zinc alters its electronic environment, leading to distinct spectral shifts. Additionally, its solubility in aqueous environments facilitates rapid diffusion, promoting efficient zinc detection in various settings.

(αS)-5-[(Dimethylamino)sulfonyl]-α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-8-hydroxy-2-quinolinepropanoic Acid

607708-62-3sc-218532
2.5 mg
$540.00
(0)

(αS)-5-[(Dimethylamino)sulfonyl]-α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-8-hydroxy-2-quinolinepropanoic Acid exhibits remarkable coordination chemistry with zinc, forming robust chelate complexes. Its unique sulfonyl and hydroxy functional groups facilitate strong hydrogen bonding and π-π stacking interactions, enhancing stability. The compound's ability to modulate zinc's electronic properties leads to distinctive reactivity patterns, influencing catalytic pathways and reaction kinetics in various chemical environments.

ZnAF-1

321859-09-0sc-216072
5 mg
$170.00
(0)

ZnAF-1 demonstrates intriguing coordination dynamics with zinc, characterized by its ability to form stable complexes through multiple coordination sites. The presence of halide substituents enhances its reactivity, allowing for selective interactions with nucleophiles. This compound exhibits unique solubility properties, promoting efficient diffusion in various media. Its distinct electronic structure facilitates unique redox behavior, influencing reaction rates and pathways in complex chemical systems.

ZnAF-1F

443302-08-7sc-216073
sc-216073A
sc-216073B
1 mg
5 mg
25 mg
$151.00
$755.00
$2244.00
(0)

ZnAF-1F showcases remarkable ligand exchange kinetics, driven by its halide functionalities that enhance its electrophilic character. This compound engages in dynamic coordination with zinc, leading to the formation of diverse coordination geometries. Its unique steric and electronic properties allow for selective binding interactions, influencing catalytic pathways. Additionally, ZnAF-1F's solvation characteristics contribute to its reactivity, enabling efficient participation in various chemical transformations.

Ethyl 2-(2-[(E)-2-Phenyl-1-ethenyl]-6-quinolyloxy-8-p-toluenesulfonamido)acetate

316124-89-7sc-223963
1 mg
$320.00
(0)

Ethyl 2-(2-[(E)-2-Phenyl-1-ethenyl]-6-quinolyloxy-8-p-toluenesulfonamido)acetate exhibits intriguing coordination behavior with zinc, characterized by its ability to form stable chelates. The compound's aromatic and quinoline moieties enhance π-π stacking interactions, promoting effective electron transfer. Its unique sulfonamide group facilitates hydrogen bonding, influencing the reactivity and selectivity in metal-mediated processes. This compound's solubility in organic solvents further enhances its versatility in coordination chemistry.

Ethyl 2-[2-(2-Methyl-1-propenyl)-6-quinolyloxy-8-p-toluenesulfonamido)acetate

316124-90-0sc-223964
1 mg
$320.00
(0)

Ethyl 2-[2-(2-Methyl-1-propenyl)-6-quinolyloxy-8-p-toluenesulfonamido]acetate demonstrates remarkable reactivity as a zinc complexing agent. The presence of the quinoline structure allows for strong π-π interactions, while the sulfonamide functionality introduces polar characteristics that enhance solvation dynamics. This compound's ability to engage in ligand exchange reactions is notable, facilitating rapid kinetics in coordination environments. Its unique architecture promotes selective binding, making it a fascinating subject for studies in metal-ligand interactions.