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Isopulegyl formate is a natural organic compound with the chemical formula C11H20O2, derived from the organic compound isopulegol found in certain essential oils, particularly oil of Calamintha nepeta. It is known for its pleasant minty, herbaceous aroma and is recognized for its potential as a bioactive compound with antimicrobial and insecticidal properties.

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  • 10588-15-5 Structure
  • Basic information

    1. Product Name: isopulegyl formate
    2. Synonyms: isopulegyl formate;Formic acid (1R)-5β-methyl-2α-(1-methylethenyl)cyclohexan-1β-yl ester
    3. CAS NO:10588-15-5
    4. Molecular Formula: C11H18O2
    5. Molecular Weight: 182.25942
    6. EINECS: 234-192-4
    7. Product Categories: N/A
    8. Mol File: 10588-15-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 232°Cat760mmHg
    3. Flash Point: 88.2°C
    4. Appearance: /
    5. Density: 0.94g/cm3
    6. Vapor Pressure: 0.0603mmHg at 25°C
    7. Refractive Index: 1.458
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: isopulegyl formate(CAS DataBase Reference)
    11. NIST Chemistry Reference: isopulegyl formate(10588-15-5)
    12. EPA Substance Registry System: isopulegyl formate(10588-15-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 10588-15-5(Hazardous Substances Data)

10588-15-5 Usage

Uses

Used in Food and Beverage Industry:
Isopulegyl formate is used as a flavoring agent for its pleasant minty, herbaceous aroma, enhancing the taste and aroma of various food and beverage products.
Used in Fragrance Industry:
In the fragrance industry, isopulegyl formate is used to add a fresh and cooling note to perfumes and colognes, contributing to the overall scent profile and providing a refreshing quality to the fragrances.
Used in Natural Pest Control Products:
Isopulegyl formate has potential as a bioactive compound with insecticidal properties, making it a promising candidate for use in natural pesticide products, offering an alternative to synthetic pesticides.
Used in Antimicrobial Products:
Due to its antimicrobial properties, isopulegyl formate can be utilized in the development of natural antimicrobial products, providing a broad-spectrum antimicrobial effect for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 10588-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,8 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10588-15:
(7*1)+(6*0)+(5*5)+(4*8)+(3*8)+(2*1)+(1*5)=95
95 % 10 = 5
So 10588-15-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H18O2/c1-8(2)10-5-4-9(3)6-11(10)13-7-12/h7,9-11H,1,4-6H2,2-3H3

10588-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-methyl-2-prop-1-en-2-ylcyclohexyl) formate

1.2 Other means of identification

Product number -
Other names EINECS 234-192-4

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:10588-15-5 SDS

10588-15-5Downstream Products

10588-15-5Relevant articles and documents

Novel photolactonisation from xanthenoic esters

Plessis, Caroline,Derrer, Sam

, p. 6519 - 6522 (2007/10/03)

In the context of our work on photocleavable fragrance precursors, we have discovered a new photo-fragmentation of xanthenoic esters into xanthene- and formyl radicals. This homolytic cleavage has not been reported previously. Thus, unsaturated formyl radicals cyclise to lactones of various ring size.

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