Decarbonylation colchicine

97%

Reagent Code: #67765
label
Alias N-deacetyl-N-methylcolchicine; decarboxycolchicine; colchamide colchicine; decarbocolchicine; decarboxycolchicine (>98%, BR); N-deacetyl-N - Methylcolchicine solution; Demethacin solution
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CAS Number 477-30-5
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Properties DMSO: 10 mg/mL

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 371.43 g/mol
Formula C₂₁H₂₅NO₅
badge Registry Numbers
EC Number 207-514-6
MDL Number MFCD00075459
thermostat Physical Properties
Melting Point 73-75℃
Boiling Point 501.11℃ (rough estimate)
inventory_2 Storage & Handling
Density 1.235 g/ml (rough estimate)
Storage 2-8°C, inert gas, protected from light

description Product Description

Decarbonylation colchicine is primarily utilized in research settings to study its effects on cellular processes, particularly in the context of microtubule dynamics. It serves as a valuable tool for investigating the mechanisms of cell division and the role of microtubules in maintaining cell structure and function. Researchers often employ it to explore its potential in inhibiting mitosis, which can provide insights into cancer therapy development. Additionally, it is used in biochemical studies to understand the interaction between colchicine derivatives and tubulin, aiding in the design of more effective therapeutic agents. Its application is largely confined to experimental and preclinical studies, contributing to advancements in cell biology and pharmacology.

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Test Parameter Specification
Appearance light yellow powder
Purity 96.5-100
Loss on Drying 0-3.0%
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿28,200.00
Decarbonylation colchicine
Decarbonylation colchicine is primarily utilized in research settings to study its effects on cellular processes, particularly in the context of microtubule dynamics. It serves as a valuable tool for investigating the mechanisms of cell division and the role of microtubules in maintaining cell structure and function. Researchers often employ it to explore its potential in inhibiting mitosis, which can provide insights into cancer therapy development. Additionally, it is used in biochemical studies to understand the interaction between colchicine derivatives and tubulin, aiding in the design of more effective therapeutic agents. Its application is largely confined to experimental and preclinical studies, contributing to advancements in cell biology and pharmacology.
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