1079-01-2 Usage
Description
FEMA 3765, also known as Myrtenyl acetate, is a chemical compound derived from various plant sources such as peppermint oil, Myrtus communis, Scotch spearmint oil, juniper essential leaf oil, Hyssopus officinalis L. essential oil, Ormenis mixta essential oil, thyme, juniper berry, myrtle leaf and berry, and buchu oil. It is characterized by its fresh, woody, minty odor and a fresh, woody, herbaceous, carrot taste. Myrtenyl acetate has a taste threshold value of 10 ppm and is known for its woody, cedar-like taste with floral, green, and cooling nuances.
Uses
Used in Flavor and Fragrance Industry:
FEMA 3765 is used as a flavoring agent for its woody, cedar-like taste with floral, green, and cooling nuances. It is commonly used in the creation of various food and beverage products to enhance their taste and aroma.
FEMA 3765 is also used as a fragrance ingredient for its fresh, woody, minty odor. It is widely utilized in the perfumery and cosmetics industry to create unique and appealing scents for various products such as perfumes, colognes, and other personal care items.
Used in Aromatherapy:
Due to its refreshing and invigorating properties, FEMA 3765 is used in aromatherapy as a natural remedy to promote relaxation, reduce stress, and improve overall well-being. Its woody, minty, and herbaceous characteristics make it a popular choice for creating a calming and soothing atmosphere.
Used in Essential Oils:
FEMA 3765 is used as a component in various essential oils, contributing to their unique aroma and therapeutic properties. It is commonly found in essential oils derived from plants such as peppermint, myrtle, juniper, and thyme, which are known for their numerous health benefits and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1079-01-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1079-01:
(6*1)+(5*0)+(4*7)+(3*9)+(2*0)+(1*1)=62
62 % 10 = 2
So 1079-01-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O2/c1-8(13)14-7-9-4-5-10-6-11(9)12(10,2)3/h4,10-11H,5-7H2,1-3H3/t10-,11-/m1/s1
1079-01-2Relevant articles and documents
First synthesis of hydroxy-pinonaldehyde and hydroxy-pinonic acid, monoterpene degradation products present in atmosphere
Fache, Fabienne,Piva, Olivier,Mirabel, Philippe
, p. 2511 - 2513 (2002)
Hydroxy-pinonaldehyde and hydroxy-pinonic acid, monoterpene degradation products have been for the first time isolated by synthesis and fully characterized. The key step of the synthesis is an oxidation using the RuCl3/NaIO4 system.
Continuous-Flow Chemo and Enzymatic Synthesis of Monoterpenic Esters with Integrated Purification
Adarme, Carlos A.A.,Le?o, Raquel A.C.,de Souza, Stefania P.,Itabaiana, Ivaldo,de Souza, Rodrigo O.M.A.,Rezende, Claudia M.
, p. 39 - 46 (2018/05/22)
Monoterpenic esters are very important flavor and fragrance compounds due to their organoleptic properties. Despite their importance, many drawbacks are found for the production of monoterpenic esters. Here in we report two different approach's (chemo and enzymatic) for the continuous production of monoterpenic esters with integrated purification arriving on the desired molecules with high yields (>95%) and short reaction times.
Oxidation of α-pinene by atmospheric oxygen in the supercritical CO2-ethyl acetate system in the presence of Co(II) complexes
Anikeev,Ilina,Kurbakova,Nefedov,Volcho,Salakhutdinov
experimental part, p. 190 - 195 (2012/03/12)
The reactivity of monoterpene α-pinene in a flow reactor in the presence of cobalt catalyst in a complex supercritical solvent consisting of CO2 and ethyl acetate is studied over the temperature range of 190-320°C and a pressure range of 110-125 atm. It was found that the main isomerization products include compounds with bicyclo[2.2.1]heptane and p-menthane backbones; the reaction is accompanied by partial racemization. The formation of oxidation products is observed in the presence of air, with epoxydation rather than allylic oxidation being the predominant process at the first stage. The oxidized products (campholenic aldehyde, verbenone, pinocamphone) are shown to be formed with a high enantioselectivity; the formation of acetoxylation products is observed at temperatures above 200°C.
