quinmerac
8-quinolinecarboxylic acid, 7-chloro-3-methyl-
 
Notes:
None found
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CAS Number: 90717-03-6Picture of molecule3D/inchi
ECHA ELINCS - REACH Pre-Reg: 402-790-6
FDA UNII: 0OFY83UPMH
Nikkaji Web: J661.713A
Beilstein Number: 8392904
MDL: MFCD00145199
XlogP3-AA: 2.70 (est)
Molecular Weight: 221.64216000
Formula: C11 H8 Cl N O2
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: herbicides / pesticides
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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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)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
Carbosynth
For experimental / research use only.
Quinmerac
Santa Cruz Biotechnology
For experimental / research use only.
Quinmerac
Sigma-Aldrich
For experimental / research use only.
Quinmerac PESTANAL®, analytical standard
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
unreported-quail LD50  > 2000 mg/kg
Pesticide Manual. Vol. 9, Pg. 750, 1991.

oral-rat LD50  > 5000 mg/kg
Pesticide Manual. Vol. 9, Pg. 750, 1991.

Dermal Toxicity:
skin-rat LD50 > 2000 mg/kg
Pesticide Manual. Vol. 9, Pg. 750, 1991.

Inhalation Toxicity:
inhalation-rat LC50 > 5400 mg/m3/4H
Pesticide Manual. Vol. 9, Pg. 750, 1991.

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Safety in Use Information:
Category: herbicides / pesticides
Recommendation for quinmerac usage levels up to:
 not for fragrance use.
 
Recommendation for quinmerac flavor usage levels up to:
 not for flavor use.
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Safety References:
European Food Safety Authority (EFSA) reference(s):
Outcome of the consultation with Member States, the applicant and EFSA on the pesticide risk assessment of confirmatory data for the active substance quinmerac
View page or View pdf
Retrospective analysis of the immunotoxic effects of plant protection products as reported in the Draft Assessment Reports for their peer review at EU level
View page or View pdf
Review of the existing maximum residue levels for quinmerac according to Article 12 of Regulation (EC) No 396/2005
View page or View pdf
EPI System: View
ClinicalTrials.gov: search
Daily Med: search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 91749
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 7-chloro-3-methylquinoline-8-carboxylic acid
Chemidplus: 0090717036
RTECS: VB1981800 for cas# 90717-03-6
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References:
 7-chloro-3-methylquinoline-8-carboxylic acid
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 91749
Pubchem (sid): 135049180
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEBI: View
CHEMBL: View
KEGG (GenomeNet): C18891
HMDB (The Human Metabolome Database): Search
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
7-chloro-3-methyl-8-quinolinecarboxylic acid
7-chloro-3-methylquinoline-8-carboxylic acid
8-quinolinecarboxylic acid, 7-chloro-3-methyl-
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Articles:
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.
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