acequinocyl

2-(acetyloxy)-3-dodecyl-1,4-naphthalenedione

CAS: 57960-19-7 C24 H32 O4 MW: 384.51584000

Identification

Nameacequinocyl
CAS Number57960-19-7
FDA UNIIMQN165D1MB
Molecular FormulaC24 H32 O4
Molecular Weight384.51584000
MDL NumberMFCD01938252
Nikkaji NumberJ641.768J
Beilstein2016033

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 59.60 °C. @ 760.00 mm Hg (est)
Boiling Point 504.05 °C. @ 760.00 mm Hg (est)
Vapor Pressure 1.270000 mmHg @ 25.00 °C. (est)
Flash Point 421.00 °F. TCC ( 215.90 °C. ) (est)
logP (o/w) 7.855 (est)
Soluble in water, 0.001639 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral Toxicityintraperitoneal-rat LD50 1719 mg/kg
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements', 'PERIPHERAL NERVE AND SENSATION: SPASTIC PARALYSIS WITH OR WITHOUT SENSORY CHANGE\nGASTROINTESTINAL: "HYPERMOTILITY, DIARRHEA"']

Safety in Use

Categoryherbicides / pesticides
Recommendation for acequinocyl usage levels up tonot for fragrance use.
Recommendation for acequinocyl flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

2-( acetyloxy)-3-dodecyl-1,4-naphthalenedione 3- dodecyl-1,4-dihydro-1,4-dioxo-2-naphthyl acetate 3- dodecyl-1,4-dioxo-1,4-dihydro-2-naphthalenyl acetate 3- dodecyl-1,4-dioxo-1,4-dihydronaphthalen-2-yl acetate (3- dodecyl-1,4-dioxonaphthalen-2-yl) acetate 3- dodecyl-2-hydroxy-1,4-naphthoquinone acetate kanemite 1,4- naphthalenedione, 2-(acetyloxy)-3-dodecyl 1,4- naphthalenedione, 2-(acetyloxy)-3-dodecyl- 1,4- naphthoquinone, 3-dodecyl-2-hydroxy-, acetate PubMed: Pesticide compatibility with natural enemies for pest management in greenhouse gerbera daisies. PubMed: Monitoring and risk assessment of pesticide residues in yuza fruits (Citrus junos Sieb. ex Tanaka) and yuza tea samples produced in Korea. PubMed: Chemical control of the red palm mite, Raoiella indica (Acari: Tenuipalpidae) in banana and coconut. PubMed: Parallel evolution of cytochrome b mediated bifenazate resistance in the citrus red mite Panonychus citri. PubMed: Mutations in the mitochondrial cytochrome b of Tetranychus urticae Koch (Acari: Tetranychidae) confer cross-resistance between bifenazate and acequinocyl. PubMed: Side effects of five new acaricides on the predator Galendromus occidentalis (Acari, Phytoseiidae). PubMed: Baseline susceptibility and cross resistances of some new acaricides in the European red mite, Panonychus ulmi. PubMed: Comparative acaricide susceptibility and detoxifying enzyme activities in field-collected resistant and susceptible strains of Tetranychus urticae. PubMed: Acaricide mode of action. PubMed: Determination of acequinocyl and hydroxyacequinocyl on fruits and vegetables by HPLC-DAD. PubMed: Genetic analysis and cross-resistance spectrum of a laboratory-selected chlorfenapyr resistant strain of two-spotted spider mite (Acari: Tetranychidae).