Description

Plaunotol m-4 CAS NO 95310-55-7 is a high-purity, specialized chemical compound of significant interest in advanced pharmaceutical research and development. This compound serves as a critical intermediate or active pharmaceutical ingredient (API) for the synthesis of novel therapeutic agents. It is primarily sought by research institutions, pharmaceutical manufacturers, and fine chemical suppliers engaged in developing treatments for gastrointestinal and related disorders. Our supply is characterized by stringent quality control, ensuring reliability for sensitive applications.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of gastroprotective and anti-ulcer drugs.
• Active Pharmaceutical Ingredient (API) Development: Used in R&D for formulating new drug candidates targeting mucosal defense mechanisms.
• Biochemical Research: A tool compound for studying cytoprotective pathways and mechanisms of action in cellular models.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in pharmaceutical laboratories.
• Fine Chemical Synthesis: Employed in multi-step organic syntheses to create more complex, biologically active molecules.

Basic Information

Product Name	Plaunotol m-4
CAS No.	95310-55-7
Molecular Formula	C20H34O2
Molecular Weight	306.48 g/mol
Synonyms	Plaunotol; Plaunotol M4; 2-[(1R,2R,5S,8S)-2,5,8-Trimethyl-1-[(1R)-4-methyl-3-cyclohexen-1-yl]nonyl]-1,3-propanediol; (1R,2R,5S,8S)-1-[(1R)-4-Methyl-3-cyclohexen-1-yl]-2,5,8-trimethylnonane-1,9-diol; 1,9-Nonanediol, 1-[(1R)-4-methyl-3-cyclohexen-1-yl]-2,5,8-trimethyl-, (1R,2R,5S,8S)-; Kelnac (trade name component); Gastroprotective diterpenoid
EINECS	Contact for details

Quality Control

Our Plaunotol m-4 is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation (IR, NMR), to ensure it meets the high standards required for pharmaceutical applications. A comprehensive Certificate of Analysis (COA) detailing purity, assay, and impurity profiles is provided with every shipment. We adhere to cGMP principles where applicable to support our global clientele in regulated industries.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability and potency. Keep the container tightly sealed when not in use to prevent any potential contamination or moisture uptake.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.