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11-(tert-Butoxycarbonylamino)undecanoic acid(CAS#10436-25-6)

Chemical Property:

Molecular Formula C16H31NO4
Molar Mass 301.422
Density 1.006±0.06 g/cm3(Predicted)
Melting Point 67-68 °C
Boling Point 441.9±18.0 °C(Predicted)
BRN 1975656
pKa 4.78±0.10(Predicted)
Storage Condition Sealed in dry,Room Temperature

Product Detail

Product Tags

Hazard Symbols Xi - Irritant
Risk Codes 36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description S22 - Do not breathe dust.
S24/25 - Avoid contact with skin and eyes.
WGK Germany 3
Hazard Class IRRITANT

 

Introduction

Tert-butoxycarbonyl-11-aminoundecanoic acid (BOC-11-aminoundecanoic acid) is an organic compound. It is a white solid that is soluble in organic solvents such as ether or chloroform. BOC-11-aminoundecanoic acid has a variety of uses and is mainly used as a protecting group in organic synthesis. The tert-butoxycarbonyl group (BOC) is a commonly used protective group that protects the amino group from accidental reactions or side reactions during synthesis. The preparation method of BOC-11-aminoundecanoic acid is generally obtained by esterification reaction with aminoundecanoic acid. Tert-butyl tert-butyl ether carbonyl copper chloride (BOC-Cl) was added to the solution of aminoundecanoic acid, and the reaction was carried out under carbonate buffer conditions to obtain BOC-11-aminoundecanoate. Then, BOC-11-aminoundecanoic acid is obtained by alkaline hydrolysis. The safety information of BOC-11-aminoundecanoic acid has not been clearly reported. In general, appropriate personal protective equipment, such as lab gloves and protective glasses, should be worn when handling chemicals to prevent direct contact or inhalation. It should be kept in a cool, dry, well-ventilated place and away from fire and combustible substances. When using BOC-11-aminoundecanoic acid, proper handling methods and laboratory safety guidelines must be followed.

Application
11-(tert-Butoxycarbonylamino)undecanoic acid (Boc-11-aminoundecanoic acid, CAS 10436-25-6) is a long-chain ω-amino fatty acid with a Boc-protected terminal amine. It serves as a versatile building block for the synthesis of PEGylated linkers, antibody-drug conjugates (ADCs), and bioconjugates. The carboxylic acid group enables amide or ester bond formation, while the Boc group allows selective deprotection under mild acidic conditions. This compound is widely used in drug delivery systems to attach therapeutic agents to targeting moieties, improving pharmacokinetics and reducing off-target toxicity. It also finds applications in the preparation of self-assembled monolayers (SAMs), surface coatings, and hydrogel crosslinkers. In pharmaceutical R&D, it is utilized to synthesize long-chain aliphatic prodrugs, enzyme inhibitors, and fatty acid-modified peptides. Its high purity (≥98%) ensures reproducibility in complex conjugation chemistry. Xinchem offers custom synthesis, custom chemical synthesis, and contract manufacturing of this key intermediate with flexible scaling from R&D to commercial tons. Contact us today for a competitive quote and reliable global supply.


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