Cas no 171869-95-7 (Palmatine Chloride)

Palmatine Chloride structure
Palmatine Chloride structure
Product Name:Palmatine Chloride
CAS No:171869-95-7
MF:C21H24ClNO5
MW:405.871965408325
MDL:MFCD00150276
CID:65904
PubChem ID:24862239
Update Time:2025-07-21

Palmatine Chloride Chemical and Physical Properties

Names and Identifiers

    • Palmatine chloride hydrate
    • Palmatine chloride
    • Palmatine hydrochloride
    • 2,3,9,10-tetramethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium,chloride,hydrate
    • PotassiuM bicarbonate
    • Dibenzo[a,g]quinolizinium,5,6-dihydro-2,3,9,10-tetramethoxy-, chloride, monohydrate (9CI)
    • BUFFER SP2
    • Hydrochloric PalMatine
    • KIT DNA
    • RNA EZ-96 1X96 TESTS
    • PALMATINECHLORIDE95%
    • KIT DNA/RNA EZ-96 1X96 TESTS
    • PalMatine chloride hydrate 97%
    • Dibenzo(a,g)quinolizinium, 5,6-dihydro-2,3,9,10-tetramethoxy-, chloride, hydrate (1:1:1)
    • Palmatine hydrochloride hydrate
    • NCGC00248731-01
    • Tox21_200059
    • UNII-ZMR2H7M7PK
    • Palmatine chloride monohydrate
    • PALMATINE CHLORIDE 95%
    • Q27295751
    • NCGC00257613-01
    • DTXCID1027845
    • ZMR2H7M7PK
    • 171869-95-7
    • CHEMBL2163795
    • 2,3,9,10-tetramethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium;chloride;hydrate
    • 2,3,9,10-tetramethoxy-5,6-dihydroisoquinolino[3,2-a]isoquinolin-7-ium chloride hydrate
    • Palmatine (chloride hydrate)
    • CAS-171869-95-7
    • AKOS015968461
    • Palmatine chloride hydrate, 97%
    • DTXSID1047869
    • Dibenzo(a,g)quinolizinium, 5,6-dihydro-2,3,9,10-tetramethoxy-, chloride, monohydrate
    • SCHEMBL3321462
    • PIQNSCSNSSZUIT-UHFFFAOYSA-M
    • Palmatine Chloride
    • MDL: MFCD00150276
    • Inchi: 1S/C21H22NO4.ClH.H2O/c1-23-18-6-5-13-9-17-15-11-20(25-3)19(24-2)10-14(15)7-8-22(17)12-16(13)21(18)26-4;;/h5-6,9-12H,7-8H2,1-4H3;1H;1H2/q+1;;/p-1
    • InChI Key: PIQNSCSNSSZUIT-UHFFFAOYSA-M
    • SMILES: [Cl-].O(C)C1C(=CC2=C(C=1)CC[N+]1C=C3C(=C(C=CC3=CC=12)OC)OC)OC.O

Computed Properties

  • Exact Mass: 405.13400
  • Monoisotopic Mass: 405.1343006g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 28
  • Rotatable Bond Count: 4
  • Complexity: 475
  • Covalently-Bonded Unit Count: 3
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Topological Polar Surface Area: 41.8

Experimental Properties

  • Color/Form: Yellow powder
  • Melting Point: 206-207 oC (dec.)
  • Boiling Point: No data available
  • Flash Point: 113 oC
  • PSA: 50.03000
  • LogP: 0.32450
  • Vapor Pressure: No data available
  • Solubility: Not determined

Palmatine Chloride Security Information

  • Symbol: GHS07
  • Signal Word:Warning
  • Hazard Statement: H302,H315,H319,H332
  • Warning Statement: P305+P351+P338
  • Hazardous Material transportation number:UN 2811
  • WGK Germany:3
  • Hazard Category Code: R20/22;R36/38
  • Safety Instruction: S24; S45
  • Hazardous Material Identification: Xn
  • Storage Condition:Store at 4°C,-4At ℃Store…Better
  • Safety Term:S24;S45
  • Risk Phrases:R20/22; R36/38

Palmatine Chloride Pricemore >>

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Additional information on Palmatine Chloride

Comprehensive Guide to Palmatine Chloride (CAS No. 171869-95-7): Properties, Applications, and Research Insights

Palmatine Chloride (CAS No. 171869-95-7) is a bioactive alkaloid derived from natural sources such as Berberis and Coptis plants. Known for its vibrant yellow color and diverse pharmacological properties, this compound has garnered significant attention in modern research. With the rise of interest in natural products and plant-based therapeutics, Palmatine Chloride is increasingly studied for its potential health benefits, including antioxidant, anti-inflammatory, and metabolic regulatory effects.

The chemical structure of Palmatine Chloride features a quaternary isoquinoline backbone, which contributes to its stability and bioactivity. Researchers are particularly interested in its role in gut microbiota modulation and glucose metabolism, topics trending in nutritional science and functional food industries. Recent studies also explore its synergy with other berberine-type alkaloids, a hot topic in phytochemical synergy research.

In the pharmaceutical sector, Palmatine Chloride is investigated for its potential in cardiovascular health and neuroprotection, aligning with growing consumer demand for natural alternatives to synthetic drugs. Its mechanism of action, particularly in AMPK pathway activation, is a frequent subject in PubMed and Google Scholar queries. Additionally, its application in cosmeceuticals for skin brightening and anti-aging formulations reflects the booming clean beauty movement.

From an industrial perspective, Palmatine Chloride is valued for its high purity standards (≥98% by HPLC) and compatibility with green chemistry extraction methods. Manufacturers emphasize sustainable sourcing to meet the demands of eco-conscious consumers. Analytical techniques like LC-MS and NMR are critical for quality control, ensuring compliance with USP and EP monographs.

Emerging trends highlight its potential in personalized medicine, especially for type 2 diabetes management, a frequently searched health topic. Comparative studies with berberine HCl often appear in patient forums and health blogs, underscoring public interest. Future research may focus on nanocarrier delivery systems to enhance bioavailability, a cutting-edge area in pharmaceutical technology.

In summary, Palmatine Chloride (CAS No. 171869-95-7) bridges traditional medicine and modern science, offering multifaceted applications. Its alignment with holistic wellness trends and rigorous scientific validation positions it as a compound of enduring relevance in biomedical research and nutraceutical development.

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