Description

(6E,10E,R)-3,7,11,15-Tetramethyl-6,10,14-Hexadecatrien-1-Ol CAS NO 36237-66-8 is a high-purity, optically active isoprenoid alcohol, specifically the (R)-enantiomer of farnesol. This compound is a critical chiral building block and intermediate in the synthesis of complex natural products, vitamins, and fine chemicals. It is essential for R&D and production in the pharmaceutical, fragrance, and specialty chemical industries, where precise stereochemistry and high purity are paramount for product efficacy and quality.

Application

• Pharmaceutical Intermediate: Key chiral precursor in the synthesis of vitamins (e.g., Vitamin E, Vitamin K), coenzyme Q10, and other biologically active terpenoids.
• Fragrance & Flavor Ingredient: Used as a building block for creating specific, high-value scent molecules and flavor compounds in perfumery and food flavoring.
• Agrochemical Synthesis: Intermediate in the production of certain pesticides and plant growth regulators that utilize isoprenoid structures.
• Organic Synthesis & Research: A valuable reagent in academic and industrial laboratories for stereoselective synthesis and the study of terpene chemistry.
• Cosmetic Ingredients: Potential intermediate for synthesizing skin-conditioning agents and antioxidants used in advanced cosmetic formulations.
• Material Science: Monomer or precursor for specialized polymers and liquid crystals requiring specific molecular geometry.

Basic Information

Item	Detail
Product Name	(6E,10E,R)-3,7,11,15-Tetramethyl-6,10,14-Hexadecatrien-1-Ol
CAS No.	36237-66-8
Molecular Formula	C20H34O
Molecular Weight	290.49 g/mol
Synonyms	(R)-Farnesol; (R)-(+)-Farnesol; (6E,10E)-3,7,11,15-Tetramethyl-1,6,10,14-hexadecatetraen-3-ol (R-enantiomer); (R)-3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraen-1-ol; (2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol (related isomer); trans,trans-Farnesol (racemic mixture); All-trans-farnesol
EINECS	Contact for details

Quality Control

Our (6E,10E,R)-Farnesol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including chiral HPLC, GC, and NMR, to ensure high enantiomeric purity and chemical identity. Certificates of Analysis (COA) detailing purity, specific rotation, and impurity profiles are provided with every shipment. We adhere to cGMP principles where applicable to support our clients in regulated industries.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen or argon) at 2-8°C to minimize oxidation and degradation. For long-term storage, keep the material frozen at -20°C. The container should be kept in a cool, dry, and well-ventilated area away from heat and ignition sources.

Specification

Item	Specification
Appearance	Colorless to pale yellow viscous liquid
Identification (IR)	Conforms to structure
Purity (GC/HPLC)	≥ 95.0%
Enantiomeric Excess (Chiral HPLC)	≥ 98.0% (R)
Specific Rotation [α]	+1.5° to +3.5° (c=1 in CHCl3)
Water Content (KF)	≤ 0.5%
Residual Solvents (GC)	Meets ICH guidelines

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