You Searched For: trans-Crotonyl+chloride


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Supplier: Thermo Scientific
Description: CAS No.: 625-35-4
Catalog Number: (8.20351.0025)
Supplier: Merck
Description: Crotonoyl chloride cis- and trans-mixture for synthesis, Sigma-Aldrich®
UOM: 1 * 25 mL

MSDS


Supplier: Apollo Scientific
Description: Crotonoyl chloride mixture of isomers 96%

Supplier: Thermo Scientific
Description: Crotonoyl chloride 90% remainder mainly cis-isomer, Technical Grade
Catalog Number: (8.00236.0100)
Supplier: Merck
Description: trans-Cinnamoyl chloride for synthesis, Sigma-Aldrich®
UOM: 1 * 100 mL

MSDS


Supplier: Thermo Scientific
Description: trans-Cinnamoyl chloride ≥97%
Catalog Number: (APOSOR924248-100G)
Supplier: Apollo Scientific
Description: trans-Cinnamoyl chloride 95%
UOM: 1 * 100 g


Catalog Number: (H32403.03)
Supplier: Thermo Scientific
Description: trans-3-(Trifluoromethyl)cinnamoyl chloride ≥99%
UOM: 1 * 1 g

Supplier: Apollo Scientific
Description: trans-3-(Trifluoromethyl)cinnamoyl chloride 97%

Catalog Number: (BOSSBS-13312R)
Supplier: Bioss
Description: GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.
UOM: 1 * 100 µl


Supplier: Thermo Scientific
Description: trans-Bis(triphenylphosphine)palladium(II) chloride (≥14,0% Pd)
Supplier: Thermo Scientific
Description: Cinnamoyl chloride predominantly trans 98%
Supplier: Merck
Description: Bis(triphenylphosphine)palladium(II) chloride for synthesis, Sigma-Aldrich®
Supplier: Thermo Scientific
Description: trans-Bis(triphenylphosphine)palladium(II) chloride ≥99.95% (metals basis) Pd ≥ 14.7%, Premion®
Catalog Number: (BOSSBS-13312R-FITC)
Supplier: Bioss
Description: GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-13312R-A750)
Supplier: Bioss
Description: GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.
UOM: 1 * 100 µl


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
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The original product is no longer available. The replacement shown is available.
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