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ITEM#: 3042-104094100ML
MFR#: 104094-100ML
Piperidine can be prepared either by nickel catalyzed hydrogenation of pyridine or by cobalt catalyzed hydrogenolysis of tetrahydrofurylamine It forms adducts with α,β,γ,δ-tetraphenylporphyriniron(II) and protoporphyriniron(II). Mossbauer
| Product Name | Description | Item# | QTY | |
|---|---|---|---|---|
Piperidine
|
Piperidine can be prepared either by nickel catalyzed hydrogenation of pyridine or by cobalt catalyzed hydrogenolysis of tetrahydrofurylamine It forms adducts with α,β,γ,δ-tetraphenylporphyriniron(II) and protoporphyriniron(II). Mossbauer | 3042-104094500ML | EA | |
Piperidine
|
Piperidine >=99.5%, purified by redistillation | 3042-4110271L | EA | |
Piperidine
|
Piperidine can be prepared either by nickel catalyzed hydrogenation of pyridine or by cobalt catalyzed hydrogenolysis of tetrahydrofurylamine It forms adducts with α,β,γ,δ-tetraphenylporphyriniron(II) and protoporphyriniron(II). Mossbauer | 3042-1040941L | EA | |
Piperidine
|
Piperidine, a heterocyclic cyclohexane is a volatile secondary amine. Maxam-Gilbert chemical method, a DNA sequencing technology employs piperidine to rupture DNA strands at damaged base site. Its crystal structure analyzed at 150K shows hydrogen bon | 3042-571261450ML | EA | |
Piperidine
|
Piperidine, a heterocyclic cyclohexane is a volatile secondary amine. Maxam-Gilbert chemical method, a DNA sequencing technology employs piperidine to rupture DNA strands at damaged base site. Its crystal structure analyzed at 150K shows hydrogen bon | 3042-571261200ML | EA |