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Description: Propionyl chloride ≥98%
Catalog Number: A10940.36
UOM: 1 * 500 g
Supplier: Thermo Fisher Scientific

Description: Propionyl chloride 98%
Catalog Number: ACRO131535000
UOM: 1 * 500 g
Supplier: Thermo Fisher Scientific

MSDS


Description: Propionyl chloride 99.5% phosgene-free
Catalog Number: 458975000.
UOM: 1 * 500 g
Supplier: Thermo Fisher Scientific


Description: 3-(4-Methoxyphenyl)propionyl chloride 95%
Catalog Number: APOSOR937079-1G
UOM: 1 * 1 g
Supplier: Apollo Scientific


Description: 3-(Methylthio)propionyl chloride 95%
Catalog Number: APOSOR921893-25G
UOM: 1 * 25 g
Supplier: Apollo Scientific


Description: 3-(4-Methoxyphenyl)propionyl chloride 99%
Catalog Number: H50416.03
UOM: 1 * 1 g
Supplier: Thermo Fisher Scientific

Description: 2-[4-(Isobutyl)phenyl]propionyl chloride
Catalog Number: APOSOR0555-500MG
UOM: 1 * 500 mg
Supplier: Apollo Scientific


Description: Propionyl chloride, Sigma-Aldrich®
Catalog Number: SIALP51559-500G
UOM: 1 * 500 g
Supplier: Merck


Description: Propionyl fluoride 97%
Catalog Number: APOSPC3875-25G
UOM: 1 * 25 g
Supplier: Apollo Scientific


Description: Appearance: Colorless to yellow Liquid
Catalog Number: ACRO392361000
UOM: 1 * 100 g
Supplier: Thermo Fisher Scientific

MSDS


Description: (R)-(-)-4-Benzyl-3-propionyl-2-oxazolidinone 97%
Catalog Number: APOSOR14534-10G
UOM: 1 * 10 g
Supplier: Apollo Scientific


Description: (S)-(+)-4-Benzyl-3-propionyl-2-oxazolidinone
Catalog Number: APOSOR14533-25G
UOM: 1 * 25 g
Supplier: Apollo Scientific


Description: 4-(Propionyl)benzeneboronic acid 98%
Catalog Number: APOSOR7254-250MG
UOM: 1 * 250 mg
Supplier: Apollo Scientific


Description: 4-Propionyl-1H-pyrrole-2-carboxylic acid
Catalog Number: APOSOR15460-1G
UOM: 1 * 1 g
Supplier: Apollo Scientific


Description: Methyl-4-propionyl-1H-pyrrole-2-carboxylate 97%
Catalog Number: APOSOR33482-1G
UOM: 1 * 1 g
Supplier: Apollo Scientific


Description: 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.
Catalog Number: SIAL803480-50MG
UOM: 1 * 50 mg
Supplier: Merck


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