3858-43-3

Basic information

• Product Name: (1R)-(-)-Carvomenthol
• Synonyms: (1R)-(-)-Carvomenthol
• CAS NO: 3858-43-3
• Molecular Formula: C₁₀H₂₀O
• Molecular Weight: 154.24932
• Mol File: 3858-43-3.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 101.8-102 °C(Press: 14 Torr)
• Appearance: /
• Density: 0.9056 g/cm3(Temp: 13 °C)
• PKA: 15.32±0.60(Predicted)
• CAS DataBase Reference: (1R)-(-)-Carvomenthol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R)-(-)-Carvomenthol(3858-43-3)
• EPA Substance Registry System: (1R)-(-)-Carvomenthol(3858-43-3)

Safety Data

• Hazardous Substances Data: 3858-43-3(Hazardous Substances Data)

Usage

Description

(1R)-(-)-Carvomenthol, a naturally occurring monoterpenoid, is an organic compound characterized by its minty, cooling aroma. It is commonly found in the essential oils of plants such as mint and eucalyptus.
Used in Flavor and Fragrance Industry:
(1R)-(-)-Carvomenthol is used as a flavoring agent for its minty taste and as a fragrance component for its cooling aroma, contributing to the production of food flavorings, perfumes, and other scented products.
Used in Pharmaceutical Industry:
(1R)-(-)-Carvomenthol is used as an analgesic and anti-inflammatory agent for its traditional medicinal properties, making it a popular ingredient in cough drops and topical pain relief products.
Used in Over-the-Counter Medications:
(1R)-(-)-Carvomenthol is used as a respiratory aid to alleviate symptoms of colds and congestion, being a valuable component in over-the-counter medications targeting respiratory health.

Upstream product

• 20549-47-7 1R,2R,4S-(+)-isodihydrocarveol 
• 851520-66-6 (3R)-3-isopropyl-6-methyl-7-oxabicyclo[4.1.0]heptane 
• 6485-40-1 (R)-Carvone 
• 499-70-7 (-)-carvomenthone 
• 99-49-0 Carvone 
• 3792-53-8 2-methyl-5-(prop-1-en-2-yl)cyclohexanone 
• 3626-19-5 cis epoxyde du carvomenthene 
• 499-70-7 methyl-2 isopropyl-5 cyclohexanone 
• 67-56-1 methanol 
• 1197-07-5 (+/-)-trans-carveol 
• 3626-19-5 trans epoxyde du carvomenthene 
• 2244-16-8 (S)-p-mentha-6,8-dien-2-one 
• 499-71-8 carvotanacetone 
• 1195-31-9 (+)-p-menth-1-ene 

Downstream Products

• 5206-83-7 (1R,4R)-(+)-carvomenthone 
• 3858-49-9 (1R,2S,4R)-(+)-neocarvomenthol 
• 7460-78-8 2-methyl-5-(propan-2-yl)cyclohexyl acetate 

Relevant articles and documents

Simple H2-free hydrogenation of unsaturated monoterpenoids catalyzed by Raney nickel

A series of monoterpenoids (citral, carvone, menthone, camphor) as well as cyclohexanone and hex-5-en-2-one were subjected to transfer hydrogenation with PriOH/Raney nickel system at 82 or 150 °C. Among monoterpenoids, citral and carvone underwent full conversion at 82 °C within 5 h.

Radical chain reduction of alkylboron compounds with catechols

The conversion of alkylboranes to the corresponding alkanes is classically per-formed via protonolysis of alkylboranes. This simple reaction requires the use of severe reaction conditions, that is, treatment with a carboxylic acid at high temperature (>150 °C). We report here a mild radical procedure for the transformation of organoboranes to alkanes. 4-tert-Butylcatechol, a well-established radical inhibitor and antioxidant, is acting as a source of hydrogen atoms. An efficient chain reaction is observed due to the exceptional reactivity of phenoxyl radicals toward alkylboranes. The reaction has been applied to a wide range of organoboron derivatives such as B- alkylcatecholboranes, trialkylboranes, pinacolboronates, and alkylboronic acids. Furthermore, the so far elusive rate constants for the hydrogen transfer between secondary alkyl radical and catechol derivatives have been experimentally determined. Interestingly, they are less than 1 order of magnitude slower than that of tin hydride at 80 °C, making catechols particularly attractive for a wide range of transformations involving C-C bond formation.

Influence of a non-micelle-forming surfactant on the electrocatalytic hydrogenation of carvone and limonene in aqueous medium at Raney nickel electrodes

The electrocatalytic hydrogenation (ECH) of carvone (1) and limonene (8) at a Raney nickel cathode was studied in aqueous solutions containing a non-micelle-forming surfactant (didodecyldimethylammonium bromide, DDAB). The efficiency of ECH of these substrates was markedly increased compared to that observed previously with micelle-forming surfactants, and this for very low DDAB concentrations, as a consequence of strong adsorption of DDAB on the electrode. For the ECH of 8 in basic medium (pH 10), the major part of organic compounds (60-95%) was shown to be adsorbed on the electrode surface as an organic layer stabilized by an interfacial film of DDAB.