DBCO-trifluoroacetyl-amine

97%

Reagent Code: #177785
label
Alias N-[3-(11,12-didehydrodibenzo[b,f]cyclooctan-5(6H)-yl)-3-oxopropyl]-2,2,2-trifluoroacetamide
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CAS Number 1337920-23-6

science Other reagents with same CAS 1337920-23-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.34 g/mol
Formula C₂₀H₁₅F₃N₂O₂
badge Registry Numbers
MDL Number MFCD32173228
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used in bioorthogonal chemistry for site-specific protein and peptide modifications. Enables selective labeling of biomolecules in complex biological environments without interfering with native biochemical processes. Commonly applied in live-cell imaging, targeted drug delivery, and development of antibody-drug conjugates. The trifluoroacetyl group acts as a masked amine, allowing for controlled deprotection and subsequent conjugation. Ideal for sequential labeling strategies due to its stability and selective reactivity with nucleophiles under mild conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,670.00
inventory 250mg
10-20 days ฿7,920.00
inventory 1g
10-20 days ฿21,390.00

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DBCO-trifluoroacetyl-amine
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Used in bioorthogonal chemistry for site-specific protein and peptide modifications. Enables selective labeling of biomolecules in complex biological environments without interfering with native biochemical processes. Commonly applied in live-cell imaging, targeted drug delivery, and development of antibody-drug conjugates. The trifluoroacetyl group acts as a masked amine, allowing for controlled deprotection and subsequent conjugation. Ideal for sequential labeling strategies due to its stability and se

Used in bioorthogonal chemistry for site-specific protein and peptide modifications. Enables selective labeling of biomolecules in complex biological environments without interfering with native biochemical processes. Commonly applied in live-cell imaging, targeted drug delivery, and development of antibody-drug conjugates. The trifluoroacetyl group acts as a masked amine, allowing for controlled deprotection and subsequent conjugation. Ideal for sequential labeling strategies due to its stability and selective reactivity with nucleophiles under mild conditions.

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