Bromadoline buy
Bromadoline Buy: Chemical Profile & Handling Protocols
Key Properties:
-
CAS Number
67579-24-2Product Name
BromadolineIUPAC Name
4-bromo-N-[(1R,2R)-2-(dimethylamino)cyclohexyl]benzamideMolecular Formula
C15H21BrN2OMolecular Weight
325.24 g/molInChI
InChI=1S/C15H21BrN2O/c1-18(2)14-6-4-3-5-13(14)17-15(19)11-7-9-12(16)10-8-11/h7-10,13-14H,3-6H2,1-2H3,(H,17,19)/t13-,14-/m1/s1InChI Key
UFDJFJYMMIZKLG-ZIAGYGMSSA-NSMILES
CN(C)C1CCCCC1NC(=O)C2=CC=C(C=C2)BrSynonyms
4-bromo-N-(2-(dimethylamino)cyclohexyl)benzamide, bromadoline, bromadoline maleateCanonical SMILES
CN(C)C1CCCCC1NC(=O)C2=CC=C(C=C2)BrIsomeric SMILES
CN(C)[C@@H]1CCCC[C@H]1NC(=O)C2=CC=C(C=C2)Br -
Storage:
Airtight containers @ -20°C
To preserve its chemical stability and integrity, Bromadoline must be stored under well-regulated conditions—ideally in a cool, dry place away from light and moisture. Improper storage may lead to degradation or reduced potency, which can compromise the accuracy of scientific results. Due to its potent pharmacological properties, Bromadoline is intended strictly for academic and laboratory research use and is not approved for human or veterinary consumption. Proper safety protocols and legal compliance must always be followed when handling this compound.
Researcher Note: Proper handling requires institutional certification. Reference Chemical Storage Guidelines for compliant protocols.
Chemical Reactions
Bromadoline is capable of undergoing several chemical transformations that are relevant in both synthetic and analytical chemistry. Under controlled conditions, it can undergo oxidation, typically forming N-oxide derivatives when treated with oxidizing agents such as hydrogen peroxide. These reactions are useful for studying the compound’s metabolic pathways and chemical behavior. In addition, reduction reactions can be carried out using reducing agents like lithium aluminum hydride, which convert Bromadoline into corresponding secondary amines. This is particularly useful for structural modification and functional analysis in research applications.
Another significant transformation is nucleophilic substitution, especially at the bromine atom, which allows for the synthesis of a wide range of derivatives. These substitutions are commonly employed to modify the pharmacological profile or receptor affinity of the compound. Due to the compound’s reactivity and diverse functional groups, Bromadoline serves as a valuable intermediate in chemical research focused on opioid analog development, molecular interaction studies, and structure–activity relationship (SAR) investigations.
Global Legal Status (2025)
Country Restrictions:
-
🇺🇸 Bromadoline buy in USA: Schedule I analog (DEA-controlled)
-
🇬🇧 Bromadoline buy in UK: PSA Section 9 prohibited substance
-
🇦🇺 Bromadoline is a Schedule 9 poison in Australia
-
A CDSA License is Required to Buy Bromadoline in Canada
Verified Suppliers: ResearchChemSupplier.com validates researcher credentials before processing any Bromadoline buy order.
Bromadoline Buy: Pharmacological Research Applications
Active Studies:
-
μ-receptor signaling pathways
-
Reduced-addiction analgesic development
-
SAR of halogenated benzamides
Source Responsibly: Legitimate Bromadoline buy requires documented research purposes. Explore Neuropharmacology Catalog for certified compounds.
Not intended for human consumption.
U-47931E- packages are processed and sent out 24 hours after payment.
- Delivery time 3-4 business days.
- 100% delivery speed throughout Europe.
- We accept payments Via Bitcoins, Monero XMR, MoneyGram (min 500 USD), and Riamoney (min 500 USD)
- You must know the legal status of the product you order in your country.
- free shipping applies to all orders about $250
“Bromadoline is classified as a synthetic opioid compound. Preclinical studies in rat models characterize it as a selective μ-opioid receptor (MOR) agonist. While structurally similar to codeine, Bromadoline’s pharmacological profile requires further investigation to fully elucidate its properties. It is synthesized under controlled laboratory conditions to ensure high purity standards, which is critical for research integrity.
Bromadoline powder, known for its exceptional purity levels exceeding 98%, is highly suitable for use in pharmacological, biochemical, and forensic research applications. Its high purity ensures consistent and reliable results in experimental studies, making it a valuable compound in controlled laboratory environments. Bromadoline is soluble in DMSO (dimethyl sulfoxide), which provides versatility across a wide range of in vitro and in vivo research methodologies. This solubility enhances its applicability in receptor binding studies, pharmacodynamic modeling, and related bioanalytical procedures.
Similar Compounds
Bromadoline shares structural and functional similarities with several compounds, particularly within the class of opioid analgesics. While not used clinically, it is of interest in pharmacological research for its interaction with μ-opioid receptors. Below is a comparison with notable compounds across analgesic and anticoagulant classes:
| Compound Name | Class | Key Features |
|---|---|---|
| Morphine | Opioid Analgesic | Natural opioid; strong analgesic with high addiction risk |
| Fentanyl | Opioid Analgesic | Potent synthetic opioid; rapid onset and short duration |
| Warfarin | Anticoagulant | Vitamin K antagonist; widely used for blood clot prevention |
| Brodifacoum | Anticoagulant | Long-acting rodenticide; inhibits vitamin K recycling |
Uniqueness of Bromadoline
Bromadoline stands out due to its selective μ-opioid receptor agonism, offering a potential for effective pain modulation with possibly reduced addiction liability compared to traditional opioids like morphine or fentanyl. Its synthetic structure allows for chemical modifications that make it valuable in opioid receptor and SAR (structure–activity relationship) studies.
⚠️ Note: Bromadoline should not be confused with Bromadiolone, a rodenticide and anticoagulant. Though their names are similar, they are entirely different compounds with unrelated pharmacological functions.
Reviews
There are no reviews yet.