N-Acetyl-ε-caprolactam

99%(GC)

Reagent Code: #217592
label
Alias N-acetyl-2-oxohexamethyleneimine
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CAS Number 1888-91-1

science Other reagents with same CAS 1888-91-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.20 g/mol
Formula C₈H₁₃NO₂
badge Registry Numbers
MDL Number MFCD00003262
thermostat Physical Properties
Boiling Point 134°C/26mmHg(lit.)
inventory_2 Storage & Handling
Density 1.10g/ml
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of specialty polyamides and pharmaceuticals. It serves in the production of modified peptides and proteins, enhancing metabolic stability and bioavailability. Also employed in the development of enzyme inhibitors and as a protecting group in organic synthesis due to its ability to mask amine functionalities. Its ring structure allows for controlled release in prodrug designs, making it valuable in medicinal chemistry. Additionally, it finds use in polymer modification to improve thermal and mechanical properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿390.00
inventory 100g
10-20 days ฿1,060.00
inventory 500g
10-20 days ฿5,120.00
inventory 2.5kg
10-20 days ฿23,650.00

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N-Acetyl-ε-caprolactam
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Used as an intermediate in the synthesis of specialty polyamides and pharmaceuticals. It serves in the production of modified peptides and proteins, enhancing metabolic stability and bioavailability. Also employed in the development of enzyme inhibitors and as a protecting group in organic synthesis due to its ability to mask amine functionalities. Its ring structure allows for controlled release in prodrug designs, making it valuable in medicinal chemistry. Additionally, it finds use in polymer modifica

Used as an intermediate in the synthesis of specialty polyamides and pharmaceuticals. It serves in the production of modified peptides and proteins, enhancing metabolic stability and bioavailability. Also employed in the development of enzyme inhibitors and as a protecting group in organic synthesis due to its ability to mask amine functionalities. Its ring structure allows for controlled release in prodrug designs, making it valuable in medicinal chemistry. Additionally, it finds use in polymer modification to improve thermal and mechanical properties.

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