61692-84-0

Basic information

• Product Name: ISOBUTYL TIGLATE
• Synonyms: ISOBUTYL TIGLATE;2-methyl-,2-methylpropylester,(e)-2-butenoicaci;2-methyl-,2-methylpropylester,(E)-2-Butenoicacid;TIGLIC ACID ISOBUTYL ESTER;isobutyl 2-methylcrotonate;ISOBUTYL TIGLATE 98+%;tiglicacidisobutylester96+%;2-Butenoic acid, 2-methyl-, 2-methylpropyl ester, (2E)-
• CAS NO: 61692-84-0
• Molecular Formula: C₉H₁₆O₂
• Molecular Weight: 156.22
• EINECS: 262-908-5
• Product Categories: Alphabetical Listings;Flavors and Fragrances;I-L
• Mol File: 61692-84-0.mol

Chemical Properties

• Boiling Point: 182-184 °C(lit.)
• Flash Point: 153 °F
• Appearance: /
• Density: 0.899 g/mL at 25 °C(lit.)
• Refractive Index: n20/D 1.438(lit.)
• CAS DataBase Reference: ISOBUTYL TIGLATE(CAS DataBase Reference)
• NIST Chemistry Reference: ISOBUTYL TIGLATE(61692-84-0)
• EPA Substance Registry System: ISOBUTYL TIGLATE(61692-84-0)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 61692-84-0(Hazardous Substances Data)

Usage

Uses

Used in Food and Beverage Industry:
Isobutyl tiglate is used as a flavoring agent to impart a fruity and floral taste to various food and beverage products. Its pleasant aroma enhances the overall sensory experience of these products, making them more appealing to consumers.
Used in Perfumery and Cosmetics Industry:
Isobutyl tiglate is used as a fragrance ingredient in perfumes and cosmetics due to its attractive scent. It adds a fresh and floral note to these products, creating a pleasant and long-lasting aroma that is desirable in personal care products.
Used in Pest Control Products:
Isobutyl tiglate is used as an insecticidal ingredient in pest control products. Its insecticidal properties make it a potentially effective component in products designed to repel or eliminate pests, providing a natural alternative to synthetic insecticides.

Upstream product

• 80-59-1 Tiglic acid 
• 78-83-1 2-methyl-propan-1-ol 
• 876510-34-8 2-isobutoxy-2-methyl-butyric acid 
• 876510-33-7 2-isobutoxy-2-methyl-butyric acid isobutyl ester 
• 15811-72-0 1,1,1-trichloro-2-methyl-butan-2-ol 
• 35660-94-7 (E)-2-methylbut-2-enoyl chloride 

Downstream Products

• 80-59-1 Tiglic acid 

Relevant articles and documents

Asymmetric dihydroxylation of esters and amides of methacrylic, tiglic, and angelic acid: No exception to the sharpless mnemonic!

Literature findings on the facial selectivity of the Sharpless asymmetric dihydroxylation (SAD) of isobutyl angelate are contradictory and partly in conflict with the Sharpless mnemonic. We systematically screened the SAD of esters and amides of angelic, tiglic, and methacrylic acid. Enantiocontrol arose in 14 of the 15 reactions, culminating at 99 % ee for the Weinreb amide of tiglic acid. The absolute configurations of all the nonracemic products were established by (stereo)chemical correlations. Without exception, they conform to the Sharpless mnemonic.

Peroxides as plant constituents. 6. Hydroperoxides from the blossoms of Roman camomile, Anthemis nobilis L

From the ethanol extract of the blossoms of Anthemis nobilis L. (syn. Chamaemelum nobile L.), six new hydroperoxides (1-6) were isolated, besides the known 1 beta-hydroperoxyisonobilin (7). The structures were elucidated by spectroscopic methods and in some cases ascertained by synthesis. Compounds 2 and 3 show a medium antibacterial activity.