Pent-4-En-1-Amine

≥98%

Reagent Code: #227851
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CAS Number 22537-07-1

science Other reagents with same CAS 22537-07-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 85.15 g/mol
Formula C₅H₁₁N
badge Registry Numbers
MDL Number MFCD08437625
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its amine and alkene functional groups allow for versatile reactivity, enabling conjugation or further derivatization in multi-step synthesis. Commonly employed in the development of bioactive molecules where a flexible, unsaturated amine spacer is required. Widely used in click chemistry reactions, where the alkene group reacts with azides under copper catalysis to form highly specific triazole linkages. Applications include biochemical research such as protein or DNA labeling, and the development of targeted drug delivery molecules requiring site-specific conjugation. Also utilized in polymer chemistry to introduce amine functionality into materials, enhancing reactivity or adhesion properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿6,400.00
5g
10-20 days ฿31,990.00
Pent-4-En-1-Amine
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Used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its amine and alkene functional groups allow for versatile reactivity, enabling conjugation or further derivatization in multi-step synthesis. Commonly employed in the development of bioactive molecules where a flexible, unsaturated amine spacer is required. Widely used in click chemistry reactions, where the alkene group reacts with azides under copper catalysis to form highly specific tr

Used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its amine and alkene functional groups allow for versatile reactivity, enabling conjugation or further derivatization in multi-step synthesis. Commonly employed in the development of bioactive molecules where a flexible, unsaturated amine spacer is required. Widely used in click chemistry reactions, where the alkene group reacts with azides under copper catalysis to form highly specific triazole linkages. Applications include biochemical research such as protein or DNA labeling, and the development of targeted drug delivery molecules requiring site-specific conjugation. Also utilized in polymer chemistry to introduce amine functionality into materials, enhancing reactivity or adhesion properties.

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