fenazaquin

Modify Date: 2024-01-02 23:39:14

fenazaquin Structure
fenazaquin structure
Common Name fenazaquin
CAS Number 120928-09-8 Molecular Weight 306.401
Density 1.1±0.1 g/cm3 Boiling Point 461.0±33.0 °C at 760 mmHg
Molecular Formula C20H22N2O Melting Point N/A
MSDS Chinese USA Flash Point 165.1±15.6 °C
Symbol GHS06 GHS09
GHS06, GHS09
Signal Word Danger

 Names

Name fenazaquin
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.1±0.1 g/cm3
Boiling Point 461.0±33.0 °C at 760 mmHg
Molecular Formula C20H22N2O
Molecular Weight 306.401
Flash Point 165.1±15.6 °C
Exact Mass 306.173218
PSA 35.01000
LogP 5.54
Vapour Pressure 0.0±1.1 mmHg at 25°C
Index of Refraction 1.595

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
VA1382000
CHEMICAL NAME :
Quinazoline, 4-((4-(1,1-dimethylethyl)phenyl)ethoxy)-
CAS REGISTRY NUMBER :
120928-09-8
LAST UPDATED :
199806
DATA ITEMS CITED :
5
MOLECULAR FORMULA :
C20-H22-N2-O
MOLECULAR WEIGHT :
306.44

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
136 mg/kg
TOXIC EFFECTS :
Behavioral - somnolence (general depressed activity) Behavioral - coma Gastrointestinal - hypermotility, diarrhea
REFERENCE :
NTIS** National Technical Information Service. (Springfield, VA 22161) Formerly U.S. Clearinghouse for Scientific & Technical Information. Volume(issue)/page/year: OTS0543600
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1820 mg/m3/2H
TOXIC EFFECTS :
Behavioral - somnolence (general depressed activity) Behavioral - ataxia Lungs, Thorax, or Respiration - dyspnea
REFERENCE :
NTIS** National Technical Information Service. (Springfield, VA 22161) Formerly U.S. Clearinghouse for Scientific & Technical Information. Volume(issue)/page/year: OTS0543610
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1789 mg/kg
TOXIC EFFECTS :
Behavioral - somnolence (general depressed activity) Lungs, Thorax, or Respiration - dyspnea Skin and Appendages - hair
REFERENCE :
NTIS** National Technical Information Service. (Springfield, VA 22161) Formerly U.S. Clearinghouse for Scientific & Technical Information. Volume(issue)/page/year: OTS0543587
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Bird - quail
DOSE/DURATION :
>2 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
PEMNDP Pesticide Manual. (The British Crop Protection Council, 20 Bridport Rd., Thornton Heath CR4 7QG, UK) V.1- 1968- Volume(issue)/page/year: 9,363,1991

 Safety Information

Symbol GHS06 GHS09
GHS06, GHS09
Signal Word Danger
Hazard Statements H301-H332-H410
Precautionary Statements P261
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges
Hazard Codes T,N
Risk Phrases R20
Safety Phrases 37-45-60-61
RIDADR UN 2811 6.1/PG 3
RTECS VA1382000
Hazard Class 6.1

 Articles12

More Articles
Side-effects of fenazaquin on a cellular model of Paramecium.

Commun. Agric. Appl. Biol. Sci. 74(1) , 129-35, (2009)

Our biodiversity has long been preserved, but the main constituents of our environment have been particularly affected by the addition of molecules resulting from agricultural and industrial activitie...

Investigation in tea on fate of fenazaquin residue and its transfer in brew.

Food Chem. Toxicol. 44(4) , 596-600, (2006)

Fenazaquin is a non-systemic acaricide/insecticide used widely in controlling mites and other related pests in fruits, vegetables and tea. The objective of this research was to investigate the disappe...

Incidence and inheritance of resistance to METI-acaricides in European strains of the two-spotted spider mite (Tetranychus urticae) (Acari: Tetranychidae).

Pest Manag. Sci. 57(5) , 443-8, (2001)

A strain of Tetranychus urticae (Koch; Acari: Tetranychidae), collected from hops (Humulus humuli L; Cannabaceae) in England with a short history of tebufenpyrad use, exhibited resistance to four METI...

 Synonyms

4-[2-[4-(1,1-Dimethylethyl)phenyl]ethoxy]quinazoline
T66 BN DNJ EO2R DX1&1&1
Fenazachin
Fenazaquin [ISO]
MFCD01656049
Fenazaquine
4-tert-Butylphenethyl quinazolin-4-yl ether
4-((4-(1,1-Dimethylethyl)phenyl)ethoxy)quinazoline
EINECS 410-580-0
Quinazoline, 4-[2-[4-(1,1-dimethylethyl)phenyl]ethoxy]-
4-{2-[4-(2-Methyl-2-propanyl)phenyl]ethoxy}quinazoline
4-[2-(4-tert-butylphenyl)ethoxy]quinazoline
4-tert-Butylphenethylquinazolin-4-yl ether
fenazaquin
Quinazoline,4-((4-(1,1-dimethylethyl)phenyl)ethoxy)
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