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Aminoethyl-SS-ethylalcohol

  CAS No.: 15579-01-8   Cat No.: BADC-00965   Purity: ≥95% 4.5  

Aminoethyl-SS-ethylalcohol is a cleavable disulfide ADC linker with amine and alcohol functional groups for versatile antibody conjugation. Supports targeted drug delivery in ADC development with controlled release mechanisms.

Aminoethyl-SS-ethylalcohol

Structure of 15579-01-8

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Category
ADC Linker
Molecular Formula
C4H11NOS2
Molecular Weight
153.27
Shipping
Room temperature, or blue ice upon request.
Storage
Store at -5°C,keep in dry and avoid sunlight.

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

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Popular Publications Citing BOC Sciences Products
Synonyms
2-((2-aminoethyl)disulfanyl)ethan-1-ol
IUPAC Name
Canonical SMILES
C(CSSCCO)N
InChI
InChI=1S/C4H11NOS2/c5-1-3-7-8-4-2-6/h6H,1-5H2
InChIKey
OAHFAPXIBISUJB-UHFFFAOYSA-N
Solubility
10 mm in DMSO
Appearance
Solid
Shelf Life
0-4°C for short term (days to weeks), or -20°C for long term (months).
Shipping
Room temperature, or blue ice upon request.
Storage
Store at -5°C,keep in dry and avoid sunlight.
Form
Solid

Aminoethyl-SS-ethylalcohol, a versatile chemical compound, finds diverse applications in bioscience and industrial sectors. Here are four key applications presented with high perplexity and burstiness:

Pharmaceutical Synthesis: Positioned at the crossroads of pharmaceutical innovation, Aminoethyl-SS-ethylalcohol plays a pivotal role as an intermediate in synthesizing a myriad of pharmaceuticals. It contributes to the creation of active pharmaceutical ingredients (APIs) and various drug compounds. Its intricate structure enables the generation of complex molecules crucial for therapeutic effectiveness, propelling advancements in medical treatment.

Bioconjugation: Delving into the realm of bioconjugation techniques, Aminoethyl-SS-ethylalcohol acts as a bridge, linking biomolecules like proteins, peptides, or nucleic acids. This compound fosters the formation of stable bonds between disparate biological entities, enabling the development of diagnostic tools and targeted therapies. Its significance shines in crafting antibody-drug conjugates and assorted bioconjugates for cutting-edge medical research, paving the way for breakthroughs in healthcare.

Polymer Chemistry: Unveiling its versatility in polymer chemistry, Aminoethyl-SS-ethylalcohol contributes to the synthesis of specialized polymers and resins. Serving as a monomer or a functional group modifier, it imparts specific chemical properties to polymer chains. These tailored polymers find applications across industries, ranging from coatings and adhesives to biomedical devices, showcasing the compound's multifaceted utility and impact on diverse sectors.

Analytical Chemistry: Evolving as a cornerstone in analytical chemistry, Aminoethyl-SS-ethylalcohol serves as a critical reagent for detecting and quantifying targeted compounds with precision. Its role in chromatographic techniques and other analytical methodologies enhances the sensitivity and selectivity of measurements, particularly in biosciences. This lends credence to the compound's significance in enabling accurate analysis of biochemical samples, steering advancements in scientific research and application.

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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Historical Records: Azidoethyl-SS-ethylamine | BCN-PEG4-NHS ester | MC-Gly-Gly-Phe-Boc | SPDP-PEG8-NHS | Docosanedioic acid | Mal-PEG-NHS | Acid-propionylamino-Val-Cit-OH | MC-Gly-Gly-Phe-Gly | NHS-SS-biotin | Sulfo-SMCC sodium | Aminoethyl-SS-ethylalcohol
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