quinmerac

Export Excel

8-quinolinecarboxylic acid, 7-chloro-3-methyl-

CAS: 90717-03-6 C11 H8 Cl N O2 MW: 221.64216000
All Ingredients Aromatic Ingredients CAS Numbers EINECS Numbers

Identification

Namequinmerac
IUPAC7-chloro-3-methylquinoline-8-carboxylic acid
CAS Number90717-03-6
FDA UNII0OFY83UPMH
Molecular FormulaC11 H8 Cl N O2
Molecular Weight221.64216000
MDL NumberMFCD00145199
Nikkaji NumberJ661.713A
Beilstein8392904

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 244.00 °C. @ 760.00 mm Hg
Boiling Point 416.00 °C. @ 760.00 mm Hg (est)
Flash Point 402.00 °F. TCC ( 205.40 °C. ) (est)
logP (o/w) 0.780
Soluble in water, 223 mg/L @ 20 °C (exp)

No sensory data available

Safety Information

Oral/Parenteral Toxicityunreported-quail LD50 > 2000 mg/kg
Dermal Toxicityskin-rat LD50 > 2000 mg/kg
Inhalation Toxicityinhalation-rat LC50 > 5400 mg/m3/4H

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

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

No supplier data available

Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

7- chloro-3-methyl-8-quinolinecarboxylic acid 7- chloro-3-methylquinoline-8-carboxylic acid 8- quinolinecarboxylic acid, 7-chloro-3-methyl- PubMed: Chemical reactivity of quinmerac herbicide through the Fukui function. PubMed: Pesticide pressure and fish farming in barrage pond in Northeastern France Part I: site characterization and water quality. PubMed: Simultaneous determination of pesticides, biopesticides and mycotoxins in organic products applying a quick, easy, cheap, effective, rugged and safe extraction procedure and ultra-high performance liquid chromatography-tandem mass spectrometry. PubMed: Sorption-desorption of ionogenic compounds at the mineral-water interface: study of metal oxide-rich soils and pure-phase minerals. PubMed: Auxin herbicides induce H(2)O(2) overproduction and tissue damage in cleavers (Galium aparine L.). PubMed: Auxin-induced ethylene triggers abscisic acid biosynthesis and growth inhibition.