(H-Cys-betaNA)2 · 2 HCl

(H-Cys-betaNA)2 · 2 HCl is a cysteine-derived amino acid derivative present as a bis-cysteine conjugate with beta-naphthylamine (betaNA) moieties, bearing the characteristic amino acid backbone functionality. The molecule contains amino and carboxyl functional groups associated with cysteine-derived residues and is provided as a dihydrochloride salt, which indicates protonated amine sites that enhance water solubility and define salt-state handling during chemical manipulations. In research workflows, such betaNA-tagged cysteine derivatives are employed as chemically defined substrates or labeling reagents for analytical method development, fluorescence or chromophore-based detection strategies, and the preparation of more complex cysteine-containing peptide or conjugate structures through controlled functional-group chemistry.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: CP26127

CAS No:100900-22-9

Synonyms/Alias:(H-Cys-betaNA)2.2HCl;100900-22-9;L-Cystinebis(beta-naphthylamide)dihydrochloride

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M.F/Formula
C26H28Cl2N4O2S2
M.W/Mr.
563.57

(H-Cys-betaNA)2 · 2 HCl is a cysteine-derived bis-substituted reagent supplied as a dihydrochloride salt, providing a protected/activated cysteine motif linked to a beta-naphthylamine (betaNA) reporter system. This structure is commonly handled as a stable analytical/derivatization building block where the betaNA functionality enables chromogenic or fluorogenic readouts after enzymatic or chemical transformation, while the cysteine component supports selective reactivity toward thiol-related workflows. In practice, researchers use this reagent to generate measurable signals in biochemical assays and to prepare standardized cysteine-containing reference materials for method development.

1. Enzymatic Activity Assays

(H-Cys-betaNA)2 · 2 HCl is used in biochemical assay development where cysteine-dependent or thiol-associated enzymatic activity is monitored via release or conversion of the beta-naphthylamine reporter. Laboratory teams in enzymology and chemical biology frequently select this format to obtain a strong, quantifiable signal that can be followed by UV-Vis or fluorescence-based instrumentation, supporting kinetic measurements and screening workflows. The dihydrochloride salt form helps with handling consistency and reproducible preparation of assay solutions, which is important when comparing activity across conditions or reagent lots.

2. Thiol-Related Derivatization Standards

(H-Cys-betaNA)2 · 2 HCl serves as a practical reagent for preparing derivatized standards and calibration materials in analytical chemistry workflows targeting cysteine/thiol species. Analytical method developers use it to create reference compounds that reflect the reporter-bearing cysteine motif, improving reproducibility in chromatographic or spectrometric quantification. Because the betaNA group provides a direct analytical handle, the reagent is commonly incorporated into internal standard strategies for assays where derivatization efficiency and signal response must be controlled.

3. Protein and Peptide Modification Tools

(H-Cys-betaNA)2 · 2 HCl is applied in protein chemistry and peptide research as a cysteine-reactive, reporter-bearing modification tool to introduce a detectable tag onto thiol-containing biomolecules. Researchers use it to label cysteine residues in peptides or protein fragments for downstream detection, enabling comparative studies of labeling yield, sample normalization, and workflow optimization in chemical biology experiments. The reagent's salt form and cysteine motif support practical handling during labeling steps, where reproducible reaction conditions are needed for consistent readout across samples.

4. Analytical Method Development

(H-Cys-betaNA)2 · 2 HCl is frequently used during assay and analytical method development to evaluate signal generation, background behavior, and assay robustness for betaNA-based detection schemes. Instrumentation-focused teams use the reagent to benchmark detection chemistry and to establish working ranges for quantitation, particularly when developing LC-based or spectrophotometric readouts tied to cysteine-related transformations. This makes the reagent valuable for optimizing sample preparation and ensuring that measured responses track with known input levels of thiol/cysteine equivalents.

Size
1 g;5 g;
InChI
1S/C26H26N4O2S2.2ClH/c27-23(25(31)29-21-11-9-17-5-1-3-7-19(17)13-21)15-33-34-16-24(28)26(32)30-22-12-10-18-6-2-4-8-20(18)14-22;;/h1-14,23-24H,15-16,27-28H2,(H,29,31)(H,30,32);2*1H/t23-,24-;;/m0../s1
InChI Key
SVTSKSGXHPXOGU-WLKYSPGFSA-N
Canonical SMILES
C1=CC=C2C=C(C=CC2=C1)NC(=O)C(CSSCC(C(=O)NC3=CC4=CC=CC=C4C=C3)N)N.Cl.Cl

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