2,2-Dimethyl-4-oxo-3,8,11,14-tetraoxa-5-azahexadecan-16-yl 4-methylbenzenesulfonate - CAS 1246999-33-6

2,2-Dimethyl-4-oxo-3,8,11,14-tetraoxa-5-azahexadecan-16-yl 4-methylbenzenesulfonate - CAS 1246999-33-6 Catalog number: BADC-01559

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2,2-Dimethyl-4-oxo-3,8,11,14-tetraoxa-5-azahexadecan-16-yl 4-methylbenzenesulfonate is a linker widely used in antibody-drug conjugates (ADCs).

Category
ADCs Linker
Product Name
2,2-Dimethyl-4-oxo-3,8,11,14-tetraoxa-5-azahexadecan-16-yl 4-methylbenzenesulfonate
CAS
1246999-33-6
Catalog Number
BADC-01559
Molecular Formula
C20H33NO8S
Molecular Weight
447.54
Purity
95%
2,2-Dimethyl-4-oxo-3,8,11,14-tetraoxa-5-azahexadecan-16-yl 4-methylbenzenesulfonate

Ordering Information

Catalog Number Size Price Quantity
BADC-01559 -- $-- Inquiry
Description
2,2-Dimethyl-4-oxo-3,8,11,14-tetraoxa-5-azahexadecan-16-yl 4-methylbenzenesulfonate is a linker widely used in antibody-drug conjugates (ADCs).
Synonyms
T-BOc-n-amido-peg4-tos
IUPAC Name
2-[2-[2-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethoxy]ethoxy]ethoxy]ethyl 4-methylbenzenesulfonate
Canonical SMILES
CC1=CC=C(C=C1)S(=O)(=O)OCCOCCOCCOCCNC(=O)OC(C)(C)C
InChI
InChI=1S/C20H33NO8S/c1-17-5-7-18(8-6-17)30(23,24)28-16-15-27-14-13-26-12-11-25-10-9-21-19(22)29-20(2,3)4/h5-8H,9-16H2,1-4H3,(H,21,22)
InChIKey
NWLAEQSWDZYPBV-UHFFFAOYSA-N
Solubility
Moderately soluble
Shipping
Room temperature in continental US; may vary elsewhere
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pictograms
Harmful
Signal Word
Warning

2,2-Dimethyl-4-oxo-3,8,11,14-tetraoxa-5-azahexadecan-16-yl 4-methylbenzenesulfonate, a versatile chemical compound, finds wide-ranging applications in biotechnological and pharmaceutical research. Here are four key applications presented with a high degree of perplexity and burstiness:

Polymer Synthesis: Serving as a monomer or functional group in polymer synthesis, this compound plays a pivotal role in producing specialized polymers with distinct properties. These polymers, tailored for specific applications such as drug delivery systems and medical implants, leverage unique mechanical and chemical characteristics. By carefully integrating into polymer structures, it enhances the stability and functionality of the final product, amplifying its utility in various biomedical settings.

Pharmaceutical Intermediate: Positioned at the forefront of pharmaceutical research, this compound acts as a crucial intermediate in the synthesis of a spectrum of pharmaceuticals. Its inherent reactivity and capacity to form intricate molecular structures make it indispensable in driving the development of novel drugs. Pharmaceutical scientists harness its potential to introduce specific functional groups into drug candidates, optimizing their therapeutic effectiveness and bioavailability, heralding advancements in drug discovery and delivery.

Surface Modification: Delving into the realm of materials science, this compound emerges as a key player in surface modification processes aimed at enhancing biocompatibility and mitigating biofouling. By binding to surfaces, it generates a functional layer that thwarts the adherence of undesirable cells and proteins, particularly fundamental in medical devices and implants. This strategic application safeguards material functionality and ensures long-term safety for use in biological environments, underlining its significance in enhancing medical technologies.

Analytical Chemistry: Unveiling its prowess in the realm of analytical chemistry, this compound features prominently in derivatization reactions, enabling precise detection and quantification of analytes. Through the formation of stable derivatives with target compounds, it facilitates their identification using diverse analytical techniques like mass spectrometry and chromatography. This amplifies the sensitivity and specificity of analytical methods, streamlining the process of accurately measuring target compounds within intricate sample matrices, propelling advancements in analytical chemistry methodologies.

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

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