Palmitoyl Ethanolamide-d4

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Reagent Code: #62588
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CAS Number 946524-34-1

science Other reagents with same CAS 946524-34-1

blur_circular Chemical Specifications

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Weight 303.5 g/mol
Formula C₁₈H₃₃D₄NO₂
inventory_2 Storage & Handling
Storage -20°C, airtight, dry

description Product Description

Palmitoyl Ethanolamide-d4 is primarily used in research and development, particularly in the field of lipidomics and metabolic studies. It serves as a stable isotope-labeled internal standard for the quantification of Palmitoyl Ethanolamide (PEA) in biological samples using techniques like mass spectrometry. This helps in understanding the role of PEA in various physiological processes, including its anti-inflammatory and analgesic properties. Additionally, it aids in the study of endocannabinoid-like molecules and their interactions within the endocannabinoid system, contributing to advancements in pain management and neuroprotection research.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿52,840.00

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Palmitoyl Ethanolamide-d4
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Palmitoyl Ethanolamide-d4 is primarily used in research and development, particularly in the field of lipidomics and metabolic studies. It serves as a stable isotope-labeled internal standard for the quantification of Palmitoyl Ethanolamide (PEA) in biological samples using techniques like mass spectrometry. This helps in understanding the role of PEA in various physiological processes, including its anti-inflammatory and analgesic properties. Additionally, it aids in the study of endocannabinoid-like mo

Palmitoyl Ethanolamide-d4 is primarily used in research and development, particularly in the field of lipidomics and metabolic studies. It serves as a stable isotope-labeled internal standard for the quantification of Palmitoyl Ethanolamide (PEA) in biological samples using techniques like mass spectrometry. This helps in understanding the role of PEA in various physiological processes, including its anti-inflammatory and analgesic properties. Additionally, it aids in the study of endocannabinoid-like molecules and their interactions within the endocannabinoid system, contributing to advancements in pain management and neuroprotection research.

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