2-Aminohexadecanoic acid

95%

Reagent Code: #136153
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CAS Number 7769-79-1

science Other reagents with same CAS 7769-79-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.44 g/mol
Formula C₁₆H₃₃NO₂
badge Registry Numbers
MDL Number MFCD01862889
thermostat Physical Properties
Melting Point ~220 °C (dec.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in the synthesis of bioactive lipids and sphingolipid analogs for research in cell signaling and membrane biology. Serves as a building block in the development of enzyme inhibitors, particularly targeting serine palmitoyltransferase and other enzymes involved in sphingolipid metabolism. Applied in dermatological studies due to structural similarity to natural ceramide components, supporting research into skin barrier function and repair. Also explored in antimicrobial agent development owing to its long alkyl chain and amino functional group, which can interact with microbial membranes.

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inventory 1g
10-20 days ฿11,600.00

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2-Aminohexadecanoic acid
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Used in the synthesis of bioactive lipids and sphingolipid analogs for research in cell signaling and membrane biology. Serves as a building block in the development of enzyme inhibitors, particularly targeting serine palmitoyltransferase and other enzymes involved in sphingolipid metabolism. Applied in dermatological studies due to structural similarity to natural ceramide components, supporting research into skin barrier function and repair. Also explored in antimicrobial agent development owing to its

Used in the synthesis of bioactive lipids and sphingolipid analogs for research in cell signaling and membrane biology. Serves as a building block in the development of enzyme inhibitors, particularly targeting serine palmitoyltransferase and other enzymes involved in sphingolipid metabolism. Applied in dermatological studies due to structural similarity to natural ceramide components, supporting research into skin barrier function and repair. Also explored in antimicrobial agent development owing to its long alkyl chain and amino functional group, which can interact with microbial membranes.

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