Description

Didrovaltrate is a high-purity, naturally derived valepotriate compound, recognized for its specific chemical structure and biological activity profile. This compound is of significant interest for advanced research and development in the pharmaceutical and nutraceutical sectors. It serves as a critical reference standard and active ingredient for scientists and manufacturers focused on developing novel therapeutic and wellness products.

Application

• Pharmaceutical Reference Standard: Used as a certified reference material (CRM) for the qualitative and quantitative analysis of valerian-based extracts and finished products in quality control laboratories.
• Active Pharmaceutical Ingredient (API) Intermediate: Serves as a key building block or precursor in the synthesis and development of new pharmaceutical formulations targeting the central nervous system.
• Nutraceutical & Dietary Supplement Research: Employed in the formulation and efficacy studies of natural health products aimed at promoting relaxation and sleep support.
• Biochemical & Pharmacological Research: Utilized in in vitro and in vivo studies to investigate mechanisms of action, bioavailability, and metabolic pathways.
• Analytical Method Development: Acts as a critical component for developing and validating chromatographic methods (HPLC, LC-MS) for complex botanical matrices.
• Cosmeceutical Applications: Investigated for potential use in topical formulations designed for calming and anti-irritant effects.

Basic Information

Product Name	Didrovaltrate
CAS No.	18296-45-2
Molecular Formula	C22H30O8
Molecular Weight	422.47 g/mol
Synonyms	Didrovaltratum; DIHDROVALTRATE; Valtrate, dihydro-; Dihydrovaltrate; (1S,3aS,6aS,9aS,9bS)-1-[(2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,6a,9a-trimethyl-2,3,4,5,6,6a,7,8,9,9b-decahydro-1H-cyclopenta[c][1]benzopyran-4-yl 3-methylbut-2-enoate; 4-(Isovaleryloxy)dihydrovaltrate; Valtral
EINECS	Contact for details

Quality Control

Our Didrovaltrate is produced and handled under strict quality management protocols to ensure batch-to-batch consistency and reliability. Each lot undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to support your quality assurance and regulatory compliance needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time conforms to reference standard
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0%

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