155348-06-4 Usage
Uses
Used in Insect Repellent Products:
p-Menthane-1,3,8-triol is used as an active ingredient in insect repellents for its ability to effectively ward off mosquitoes, ticks, and other disease-carrying insects. Its low toxicity in mammals ensures that it is safe for use in personal care products.
Used in Personal Care Industry:
p-Menthane-1,3,8-triol is used as a key ingredient in personal care products such as candles and lotions, providing protection against insects while being safe for human use. Its incorporation into these products offers a natural and eco-friendly alternative to synthetic insect repellents.
Used in Environmental Protection:
p-Menthane-1,3,8-triol is used as a natural insect repellent in environmental protection efforts, helping to reduce the need for chemical insecticides and minimizing the impact on non-target species and ecosystems. Its effectiveness in deterring insects makes it a valuable tool in integrated pest management strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 155348-06-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,3,4 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 155348-06:
(8*1)+(7*5)+(6*5)+(5*3)+(4*4)+(3*8)+(2*0)+(1*6)=134
134 % 10 = 4
So 155348-06-4 is a valid CAS Registry Number.
155348-06-4Relevant academic research and scientific papers
Hydroxylation of (+)-menthol by Macrophomina phaseolina
Musharraf, Syed Ghulam,Ahmed, Muhammad Arif,Ali, Rahat Azher,Choudhary, Muhammad Iqbal
experimental part, p. 77 - 82 (2012/04/11)
Biotransformation of (+)-menthol with Macrophomina phaseolina led to hydroxylations at C-1, C-2, C-6, C-7, C-8 and C-9, with the C-8 position being preferentially oxidized. The resulting metabolites were identified as 8-hydroxymenthol (2), 6R-hydroxymenthol (3), 1R-hydroxymenthol (4), 9-hydroxymenthol (5), 2R,8-dihydroxymenthol (6), 8S,9-dihydroxymenthol (7), 6R,8-dihydroxymenthol (8), 1R,8-dihydroxymenthol (9) and 7,8-dihydroxymenthol (10). Metabolites 6-10 are described here for the first time. Their structures were characterized by spectroscopic analysis.
