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155348-06-4

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155348-06-4 Usage

General Description

p-Menthane-1,3,8-triol is a natural monoterpene repellent that is derived from plants. It can be isolated from the essential oils of plants such as Pelargonium graveolens (geranium) and Mentha piperita (peppermint), among others. It is most recognized in the industry as part of core ingredients of insect repellents, primarily those aimed at mosquitoes, ticks, and other disease-carrying insects. The compound proves to be highly potent in warding off insects whilst demonstrating low toxicity in mammals, making it a suitable candidate for incorporation into personal care products including candles and lotions.

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.

155348-06-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name p-Menthane-1,3,8-triol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:155348-06-4 SDS

155348-06-4Downstream Products

155348-06-4Relevant articles and documents

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.

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