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QUINMERAC

CAS No.
90717-03-6
Chemical Name:
QUINMERAC
Synonyms
bas518;FIESTA;GAVELAN;BAS113W;bas518h;QUINMERAC;bas51802h;BUTISAN STAR;7-Chloro-3-Methyl-;Estradiol Impurity 23
CBNumber:
CB8468273
Molecular Formula:
C11H8ClNO2
Molecular Weight:
221.64
MDL Number:
MFCD00145199
MOL File:
90717-03-6.mol
Last updated:2023-05-25 18:01:20

QUINMERAC Properties

Melting point 244°C
Boiling point 416.0±40.0 °C(Predicted)
Density 1.406±0.06 g/cm3(Predicted)
storage temp. Room Temperature, under inert atmosphere
solubility DMSO (Slightly), Methanol (Slightly, Sonicated)
pka -2.84±0.10(Predicted)
color Pale Yellow to Pale Beige
Merck 13,8158
BRN 8392904
LogP 0.780
FDA UNII 0OFY83UPMH
EPA Substance Registry System Quinmerac (90717-03-6)

SAFETY

Risk and Safety Statements

Hazard statements  H412
Precautionary statements  P273-P501
Hazard Codes  T
WGK Germany  2
RTECS  VB1981800
HS Code  29333990
Toxicity LD50 in rats (mg/kg): >5000 orally, >2000 dermally (Wuerzer)

QUINMERAC price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 36522 Quinmerac PESTANAL 90717-03-6 250mg $132 2024-03-01 Buy
TRC Q696500 Quinmerac 90717-03-6 5g $215 2021-12-16 Buy
Usbiological 288520 Quinmerac 90717-03-6 50mg $333 2021-12-16 Buy
Apolloscientific OR510227 7-Chloro-3-methylquinoline-8-carboxylicacid >98% 90717-03-6 5g $227 2021-12-16 Buy
American Custom Chemicals Corporation AGR0000064 QUINMERAC 95.00% 90717-03-6 250MG $445 2021-12-16 Buy
Product number Packaging Price Buy
36522 250mg $132 Buy
Q696500 5g $215 Buy
288520 50mg $333 Buy
OR510227 5g $227 Buy
AGR0000064 250MG $445 Buy

QUINMERAC Chemical Properties,Uses,Production

Chemical Properties

Crystalline Solid

Uses

Herbicide.

Uses

Auxin-type herbicide.

Definition

ChEBI: A quinolinemonocarboxylic acid that is quinoline-8-carboxylic acid carrying additional methyl and chloro substituents at positions 3 and 7 respectively. A residual herbicide used to control broad-leaved weeds on a range of crops including cereals, rape and beet.

Environmental Fate

In the field, the DT50 of quinmerac may range from 3 to 33 days. Losses due to volatilization are negligible. Soil moisture conditions greatly influence quinmerac persistence by moderating microbial degradation and soil leaching. Quinmerac is only slightly adsorbed to the soil.

Metabolism

Chemical. Quinmerac is stable to heat, light, and in aqueous solutions with pH values between 3 and 9.
Plant. The degradation and metabolic pathways of quinmerac have not been extensively studied. In plants, oxidation of the 3-methyl group to the alcohol and hydroxylation at the 2-quinoline position are the major metabolism reactions (56). These quinmerac metabolites are subsequently conjugated to carbohydrates. The quantity of quinmerac metabolized varies among species, ranging from 5% to 80% (56).
Soil. In the soil, degradation of quinmerac was similar to that observed in plants, resulting in the same oxygenated and hydroxylated metabolites.

Toxicity evaluation

Quinmerac is excreted in the urine of mammals and appears to remain primarily unmodified. The acute oral LD50 in rat is >5000 mg/kg.

90717-02-5
90717-03-6
Synthesis of QUINMERAC from Quinoline, 8-(bromomethyl)-7-chloro-3-methyl-
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bas518 7-chloro-3-methyl-8-quinolinecarboxylicaci 7-chloro-3-methyl-8-quinolinecarboxylicacid QUINMERAC 7-Chloro-3-Methyl- bas51802h bas518h BUTISAN STAR BAS113W FIESTA GAVELAN QUINMERAC PESTANAL (7-CHLORO-3-ME- THYLQ quinmerac (bsi, draft e-iso) 7-CHLORO-3-METHYLQUINOLINE-8-CARBOXYLICACID 7-Chlor-3-methyl-8-chinolincarbonsure Quinmerac@100 μg/mL in Acetonitrile Quinmerac@1000 μg/mL in Acetonitrile 8-Quinolinecarboxylic acid, 7-chloro-3-methyl- Estradiol Impurity 23 90717-03-6 Agro Products Agro-Products Aromatics Heterocycles