BUTOPYRONOXYL

BUTOPYRONOXYL Basic information
Synthesis
Product Name:BUTOPYRONOXYL
Synonyms:BUTYL-3,4-DIHYDRO-2,2-DIMETHYL-4-OXO-1,2-H-PYRAN-[6-CARBOXYLATE];BUTYL 3,4-DIHYDRO-2,2-DIMETHYL-4-OXO-2H-PYRAN-6-CARBOXYLATE;BUTYLMESITYL OXIDE;BUTYLMESITYL OXIDE OXALATE;(ALPHA,ALPHA')-DIMETHYL(ALPHA')CARBOBUTOXYDIHYDRO-(GAMMA)-PYRONE;3,4-DIHYDRO-2,2-DIMETHYL-4-OXO-2H-PYRAN-6-CARBOXYLIC ACID BUTYL ESTER;2,2-dimethyl-6-carbobutoxy-2,3-dihydro-4-pyrone;2-carbo-n-butoxy-6,6-dimethyl-5,6-dihydro-1,4-pyrone
CAS:532-34-3
MF:C12H18O4
MW:226.27
EINECS:208-535-3
Product Categories:Alphabetic;B;BI - BZ
Mol File:532-34-3.mol
BUTOPYRONOXYL Structure
BUTOPYRONOXYL Chemical Properties
Melting point 25°C
Boiling point bp760 256-270°
density 1.054 g/mL at 25 °C(lit.)
refractive index n20/D 1.477(lit.)
Fp >230 °F
storage temp. 4°C, protect from light
solubility DMSO: 100 mg/mL (441.95 mM)
form clear liquid
color Light orange to Yellow to Green
CAS DataBase Reference532-34-3
EPA Substance Registry SystemButopyronoxyl (532-34-3)
Safety Information
Risk Statements 38
Safety Statements 37/39
WGK Germany 3
RTECS UP7000000
HS Code 29329990
Hazardous Substances Data532-34-3(Hazardous Substances Data)
ToxicityLD50 in mice, rats (ml/kg): 11.6, 7.4 orally (Draize)
MSDS Information
ProviderLanguage
SigmaAldrich English
BUTOPYRONOXYL Usage And Synthesis
SynthesisTo a 25-mL flflame-dried flflask under a nitrogen atmosphere were added freshly distilled Rawal’s diene (227 mg, 1 mmol, 1.0 equivalents) and 2 mL of CHCl3. Benzaldehyde (1.5 mmol, 1.5 equivalents) was added dropwise via a gas-tight syringe. The reaction mixture was stirred at room temperature for 2 h and then diluted with 15 mL of CH2Cl2. The yellow solution was cooled to −78 °C and treated with 142 µL acetyl chloride (2 mmol, 2 equivalents). After stirring for about 30 min, saturated Na2CO3 was added. The organic layer was separated and the water phase was diluted with 15 mL of water and extracted twice with CH2Cl2. The combined organic phase was dried with MgSO4, fifiltered, and concentrated to give a yellow oil, which was subjected to flflash chromatography to afford the desired dihydropyrone in 86% overall yield. Reference: Huang, Y.; Rawal, V. H. Org. Lett. 2000, 2, 3321−3322.
Chemical PropertiesYellow to pale reddish-brown liquid; aromatic odor. Reasonably stable in air. Slowly affected by light. Insoluble in water; miscible with alcohol, chloroform, ether, glacial acetic acid.
UsesIndalon is an insect repellent.
UsesInsect repellents that can be applied directly on the skin.
DefinitionChEBI: Butopyronoxyl is a member of pyrans and a carbonyl compound.
IndicationsButopyronoxyl is not water soluble and can be applied to skin and clothing to repel biting stable flies, Lone Star ticks, dog and cat fleas, and chiggers.
HazardToxic by ingestion. May cause liver dam- age.
Safety ProfileModerately toxic by ingestion. Produces liver necrosis in experimental animals. A rmld skin irritant. See also OXALATES and ESTERS. Combustible when exposed to heat or flame. When heated to decomposition it emits acrid fumes.
BUTOPYRONOXYL Preparation Products And Raw materials
4-ETHOXY-2-BUTANONE 1,1-DIMETHYLPROPYL ETHYL ETHER methyl-2-heptenoate 2-Ethoxypropene 5,6-DIHYDRO-4H-PYRAN-2-CARBOXYLIC ACID (E)-4-OXO-PENT-2-ENOIC ACID Butyl hydroxyacetate TERT-PENTYL VINYL ETHER (+)-(S)-HEX-1-EN-5-OL 1-TERT-BUTOXY-2-METHOXYETHANE, 99 BUTYL CROTONATE N-PROPYL ACRYLATE Vinyl isopropyl ether 4-METHOXY-2-BUTANONE TRANS-2-HEPTEN-1-OL TRANS-2-HEXENOIC ACID METHYL 2-PENTENOATE (E)-4-Hexen-1-ol

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