Doxorubicin Hydrochloride

SKU:BHB11900178
Suppliers
StressMarq Biosciences Inc.
StressMarq Biosciences Inc.
Details Products
Overview
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Doxorubicin Hydrochloride is a research-grade small-molecule inducer of apoptosis supporting Cancer and Apoptosis research. Supplied as a red-orange powder with >98% purity (CAS 25316-40-9, MW 580) dissolvable in water; store at -20°C. For research use only.
Cas No. 25316-40-9
Molecular Formula C27H29NO11•HCl
Purity >98% (TLC); NMR (Conforms)
Application Notes Apoptosis Inducer
Options selector
Catalog no. Size
SIH-390-10MG 10 mg
SIH-390-50MG 50 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size (2) — 10 mg, 50 mg.
  • Lead time: options listed as “in stock at manufacturer” typically ship in 2-3 business days; other statuses may take longer.
  • Storage: -20ºC
  • Shipping: ships at ambient temperature.
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Alternative names Adriamycin
CAS no. 25316-40-9
Applications
  • Functional Assay (In Vitro)
Source Synthetic
Molecular weight 580
Molecular formula C27H29NO11•HCl
Purity >98% (TLC); NMR (Conforms)
Bioactivity Inducer
Activity
  • Inducer
Solubility May be dissolved in water (25 mg/ml); or DMSO (30 mg/ml)
SMILES [C@H]2(OC1OC(C(O)C(N)C1)C)C[C@@](O)(CC3=C2C(=C4C(=C3O)C(=O)C5=C(C4=O)C(=CC=C5)OC)O)C(=O)CO.[H+].[Cl-]
InChIKey MWWSFMDVAYGXBV-RUELKSSGSA-N
Form Red-Orange powder
Storage -20ºC
Shipping Shipped Ambient
Catalog no. (Mfr.) SIH-390
Main SKU BHB11900178

Doxorubicin Hydrochloride is a DNA-intercalating chemotherapeutic agent known for its broad-spectrum anticancer activity. In neuroscience, Doxorubicin is used to model neurotoxicity and investigate mechanisms of neuronal damage, particularly in studies of chemotherapy-induced cognitive impairment ("chemo brain"). It induces apoptosis by inhibiting topoisomerase II and disrupting DNA replication and transcription. Doxorubicin also triggers oxidative stress and mitochondrial dysfunction—key features of neurodegenerative diseases. Although its clinical use is limited by systemic toxicity, including hematologic and cardiac effects, its ability to induce autophagy and cell death pathways makes it a valuable tool for studying neuronal stress responses and neurodegeneration in vitro and in vivo.

Classification: Not WHMIS controlled.

Safety Phrases:

  • S22 - Do not breathe dust.
  • S24/25 - Avoid contact with skin and eyes.
  • S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.

Hazard statements:

  • H302- Harmful if swallowed.
  • H350- May cause cancer.

Precautionary statements:

  • P201- Obtain special instructions before use.
  • P308 + P313- IF exposed or concerned: Get medical advice/ attention.

Doxorubicin Hydrochloride (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-390)

Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.

  • Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
  • Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
  • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
  • QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
  • Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity

To quote quickly, tell us: compound name + CAS/structure (SMILES or mol file), intended assay context, solvent preference, salt/stereochemistry requirements, purity/QC level, and the amount (mg–g).

Can’t find the compound you’re looking for?
Send the CAS or structure and your specs. We can help source it, suggest close equivalents, or discuss custom synthesis with the right QC documentation (RUO).

1. Kusayanagi, T. et al. (2012). Bioorg Med Chem. 20(21): 6248-55.
2. Chen, N. T. et al. (2012). PLoS One. 7(9).
3. Patel, S. et al. (1997). Mol Pharmacol. 52(4): 658-66.
4. Cutts, S. et al. (1996). J Biol Chem. 271(10): 5422-9.
5. Danesi, R. et al. (2004). Transplant Proc. 36(3): 703-4.
6. Dirks-Naylor, A. (2013). Life Sci. 93(24): 913-6.
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