webinar
Oct. 27-28, 2025, Boston, MA, USA - Booth 114.
Read More

t-Boc-N-amido-PEG4-amine

  CAS No.: 811442-84-9   Cat No.: BADC-01164   Purity: ≥95% 4.5  

t-Boc-N-amido-PEG4-amine is a protected PEG linker with an amine functionality, useful in ADC synthesis. The Boc group ensures selective deprotection, enabling precise linker assembly, while PEG4 spacing improves solubility and flexibility of antibody-drug conjugates.

t-Boc-N-amido-PEG4-amine

Structure of 811442-84-9

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Linker
Molecular Formula
C15H32N2O6
Molecular Weight
336.42
Shipping
Room temperature
Shipping
Store at 2-8°C, protect from light

* For research and manufacturing use only. We do not sell to patients.

Size Price Stock Quantity
-- $-- In stock

Looking for different specifications? Click to request a custom quote!

Capabilities & Facilities

Popular Publications Citing BOC Sciences Products
Synonyms
Boc-NH-PEG4-CH2CH2NH2; NHBoc-PEG4-amine; O-(2-Aminoethyl)-O'-[2-(Boc-amino)ethyl]triethylene Glycol; 16-Amino-5,8,11,14-tetraoxa-2-azahexadecanoic Acid 1,1-Dimethylethyl Ester; tert-Butyl (14-amino-3,6,9,12-tetraoxatetradecyl)carbamate; N1-Boc-3,6,9,12-tetraoxatetradecane-1,14-diamine; BocNH-PEG4-NH2; 5,8,11,14-Tetraoxa-2-azahexadecanoic acid, 16-amino-, 1,1-dimethylethyl ester
IUPAC Name
tert-butyl N-[2-[2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]ethoxy]ethyl]carbamate
Canonical SMILES
CC(C)(C)OC(=O)NCCOCCOCCOCCOCCN
InChI
InChI=1S/C15H32N2O6/c1-15(2,3)23-14(18)17-5-7-20-9-11-22-13-12-21-10-8-19-6-4-16/h4-13,16H2,1-3H3,(H,17,18)
InChIKey
WCNWLERBLMBSOT-UHFFFAOYSA-N
Density
1.059±0.06 g/cm3 (Predicted)
Solubility
Soluble in DMSO (Slightly), Methanol (Slightly)
PSA
101.27000
Appearance
Pale Yellow or Colorless Oily Liquid
Shipping
Room temperature
Storage
Store at 2-8°C, protect from light
Signal Word
Danger
Boiling Point
443.9±40.0 °C at 760 mmHg
Biological Activity
Boc-NH-PEG4-CH2CH2NH2 a cleavable 5 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1] . In Vitro: ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Related Products

Contact our experts today for pricing and comprehensive details on our ADC offerings.

You May Also Be Interested In

From cytotoxin synthesis to linker design, discover our specialized services that complement your ADC projects.

ADC Linker Development Enzyme Cleavable Linker Cathepsin B Cleavable Linker/Peptide Linker Phosphatase Cleavable Linker β-Glucuronide Linker β-Galactosidase Cleavable Linker Sulfatase Cleavable Linker Chemically Cleavable Linker Non-Cleavable Linker Services Acid Cleavable Linker/Hydrazone Linker

Unlock Deeper ADC Insights

Learn more about payload design, linker strategies, and integrated CDMO support through our curated ADC content.

Linkers - A Crucial Factor in Antibody–Drug Conjugates In-Depth Review of ADC Linkers: Types, Mechanisms, and Research Progress New Structural Insights Solve Instability Issues of Maleimide Linkers in ADCs PEG Linkers in Antibody-Drug Conjugates Peptide Linkers in Antibody-Drug Conjugates Disulfide Linkers in Antibody-Drug Conjugates Biotinylation Reagents in Antibody-Drug Conjugates Maleimide Linkers in Antibody-Drug Conjugates Current ADC Linker Chemistry SPDB Linkers in Antibody-Drug Conjugates

Explore More ADC Products

Find exactly what your project needs from our expanded range of ADCs, offering flexible options to fit your timelines and goals.

ADC Cytotoxin

Powerful Targeted Cancer Solutions

ADC  Cytotoxin with Linker

Enhanced Stability And Efficacy

ADC Linker

Precise Conjugation For Success

Antibody-Drug  Conjugates (ADCs)

Maximized Therapeutic Performance

Auristatins

Next-Level Tubulin Inhibition

Calicheamicins

High-Impact DNA Targeting

Camptothecins

Advanced Topoisomerase Inhibition

Daunorubicins / Doxorubicins

Trusted Anthracycline Payloads

Duocarmycins

Potent DNA Alkylation Agents

Maytansinoids

Superior Microtubule Disruption

Pyrrolobenzodiazepines

Ultra-Potent DNA Crosslinkers

Traditional Cytotoxic Agents

Proven Chemotherapy Solutions

Cleavable Linker

Precise Intracellular Drug Release

Non-Cleavable Linker

Exceptional Long-Term Stability

Historical Records: t-Boc-N-amido-PEG1-propionic acid | t-Boc-N-amido-PEG2-bromide | t-Boc-N-amido-PEG4-propionic acid | t-Boc-N-amido-PEG4-bromide | t-Boc-N-amido-PEG4-amine
Send Inquiry
Verification code
Inquiry Basket