803480

PDPH (3-(2-pyridyldithio)propionyl hydrazide)

• Sinónimos: 3-(2-Pyridyldithio)propionate hydrazide, 3-[(2-Pyridyl)dithio]propionohydrazide
• Fórmula empírica (notación de Hill): C₈N₃S₂OH₁₁
• Número de CAS: 115616-51-8
• Peso molecular: 229.32
• Número MDL: MFCD00467204
• Código UNSPSC: 12352125
• ID de la sustancia en PubChem: 329768811
• NACRES: NA.22

Propiedades

• Análisis: ≥95%
• Nivel de calidad: 100
• formulario: powder
• mol peso: 229.32
• idoneidad de la reacción: reagent type: cross-linking reagent
• condiciones de almacenamiento: desiccated
• solubilidad: DMSO or DMF: soluble
• grupo funcional: hydrazide
• Condiciones de envío: ambient
• temp. de almacenamiento: 2-8°C
• cadena SMILES: NNC(CCSSC1=NC=CC=C1)=O
• InChI: 1S/C8H11N3OS2/c9-11-7(12)4-6-13-14-8-3-1-2-5-10-8/h1-3,5H,4,6,9H2,(H,11,12)
• Clave InChI: NITXODYAMWZEJY-UHFFFAOYSA-N

Descripción

Descripción general

The PDPH is a heterobifunctional crosslinker containing sulfhydryl-reactive pyridyldithiol and carbonyl-reactive hydrazide moieties. Pyridyldithiols react with free sulfhydryls (-SH) to form disulfide bonds. Hydrazide groups react with carbonyls (aldehydes and ketones) to form stable hydrazone bonds. Aldehyde groups can be created by periodate-oxidation of sialic acid and other sugar components of glycoprotein polysaccharides. Thus, PDPH is useful for conjugating glycoproteins and sulfhydryl-containing peptides or proteins. Likewise, PDPH is useful as a sulfhydryl-addition reagent for glycoproteins and other carbohydrates; after reaction of the hydrazide to an oxidized carbohydrate, the pyridyldithiol group can be cleaved by a reducing agent to expose a sulfhydryl group. Yet another application for PDPH is to react the primary amine of the hydrazide moiety to a carboxyl group using the crosslinker EDC.

Características y beneficios

• Reactive groups: pyridyldisulfide and hydrazide
• Reactive toward: sulfhydryl groups and carbonyl (aldehyde) groups
• Short (9.2A), sulfhydryl-to-aldehyde crosslinker with disulfide bond spacer arm (cleavable)
• Pyridyldithiol group results in attachment to sulfhydryls via disulfide bond, which can be cleaved with DTT, TCEP or other reducing agents
• Hydrazide group conjugates to oxidized sugars of glycoproteins and carbohydrates
• Use sodium meta-periodate to oxidize glycosylation (e.g., sialic acid) to reactive aldehyde groups
• Use with EDC to conjugate primary amine of hydrazide group to carboxyl groups

Precaución

This product is sensitive to moisture. The vial is packaged in a resealable bag with a desiccant to reduce exposure to moisture. After cold storage, equilibrate the vial to room temperature before opening to reduce condensation inside the vial. Make fresh solutions. Storage of stock solutions is not recommended. After use, return the vial to the resealable bag. Close the bag and store the product at the recommended temperature.

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable