7785-33-3 Usage
Description
Geranyl tiglate is a naturally occurring ester compound that possesses a pleasant, herbaceous, geranium, and fruity odor. It is characterized by its green, estry melon, and berry seedy taste with a floral and slightly fatty nuance at a concentration of 5 to 10 ppm. This organic compound is found in kumquat and geranium oil and has a fresh sweet green melon aroma with a slight harsh herbaceous melonal nuance and a powdery rosy nuance at an aroma threshold value of 1.0%.
Uses
Used in Flavor and Fragrance Industry:
Geranyl tiglate is used as a flavoring agent for its green, estry melon, and berry seedy taste characteristics. It is particularly suitable for enhancing the flavor of food products that require a fresh, fruity, and slightly fatty taste.
Used in Aromatherapy:
Geranyl tiglate is used as an aromatherapeutic agent for its pleasant, herbaceous, and fruity odor. It can be used in various aromatherapy applications, such as inhaled or topical treatments, to promote relaxation, stress relief, and a sense of well-being.
Used in Perfumery:
Geranyl tiglate is used as a fragrance ingredient in perfumery due to its fresh sweet green melon aroma with a slight harsh herbaceous melonal nuance and a powdery rosy nuance. It can be incorporated into various perfume formulations to add depth and complexity to the scent profile.
Used in Cosmetics and Personal Care Products:
Geranyl tiglate is used as a scent component in cosmetics and personal care products, such as lotions, creams, and shampoos, to provide a pleasant and refreshing fragrance experience for the user.
Used in Natural Product Formulation:
Geranyl tiglate can be used in the formulation of natural products, such as essential oils and herbal remedies, to enhance their aroma and therapeutic properties. Its natural occurrence in kumquat and geranium oil makes it a suitable candidate for use in natural product formulations.
Preparation
Prepared in a patented process by reaction of sodium hydroxide, geraniol and methyl tiglate.
Check Digit Verification of cas no
The CAS Registry Mumber 7785-33-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7785-33:
(6*7)+(5*7)+(4*8)+(3*5)+(2*3)+(1*3)=133
133 % 10 = 3
So 7785-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H24O2/c1-6-14(5)15(16)17-11-10-13(4)9-7-8-12(2)3/h6,8,10H,7,9,11H2,1-5H3/b13-10+,14-6+
7785-33-3Relevant articles and documents
Preparation of organic acids and/or esters
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, (2008/06/13)
Carboxylic acids and/or esters are prepared by converting the STR1 moiety in a 1-substituted 2,2-trihaloethanol, or derivative wherein X represents halogen and R is hydrogen or an acyl group to an organic acid and/or ester grouping of the formula STR2 wherein R' is hydrogen or alkyl of 1 to 6 carbon atoms, in the process which comprises reacting the 1-substituted 2,2,2-trihaloethanol or acylated derivative with molecular oxygen in the presence of a catalyst comprising a complex of a transition metal having an atomic number from 21-30, 39-48 or 57-80 and at least one molecule of a ligand containing trivalent nitrogen, phosphorus, arsenic or antimony. This reaction is carried out in a reaction medium comprising an alcohol or aqueous alcohol having 1 to 6 carbon atoms optionally containing an alkali metal, said alcoholic solvent also serving as a reactant source when carboxylic acid esters are formed.
