Diclofop-methyl CAS 51338-27-3

Introduction:Basic information about Diclofop-methyl CAS 51338-27-3, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Diclofop-methyl Basic information

Product Name:Diclofop-methyl
Synonyms:NOGRASS;(+or-)-methyl2-(4-(2,4-dichlorophenoxy)phenoxy)propionate;2-(4-(2,4-Dichlorophenoxy)phenoxy)-methyl-propionate;2-(4-(2,4-dichlorophenoxy)phenoxy)-propionicacimethylester;2-(4-(2’,4’-dichlorophenoxy)-phenoxy)-methyl-propionate;2-(4-(2',4'-Dichlophenoxy) phenoxy) methylpropanoate;Holgrass(Hoechst);Diclofop-Me
CAS:51338-27-3
MF:C16H14Cl2O4
MW:341.19
EINECS:257-141-8
Product Categories:HERBICIDE;DIA - DICPesticides&Metabolites;Alpha sort;D;DAlphabetic;Herbicides;Pesticides&Metabolites;Phenoxy structure;Alphabetic
Mol File:51338-27-3.mol

Diclofop-methyl Chemical Properties

Melting point 39-41°C
Boiling point 173-175°C (0.1 mbar)
density 1.3
refractive index 1.5300 (estimate)
storage temp. 0-6°C
form Solid
color White to off-white
Water Solubility 0.005 g/100 mL
Merck 13,3109
BRN 2224754
InChI1S/C16H14Cl2O4/c1-10(16(19)20-2)21-12-4-6-13(7-5-12)22-15-8-3-11(17)9-14(15)18/h3-10H,1-2H3
InChIKeyBACHBFVBHLGWSL-UHFFFAOYSA-N
SMILESCOC(=O)C(C)Oc1ccc(Oc2ccc(Cl)cc2Cl)cc1
LogP4.620
CAS DataBase Reference51338-27-3(CAS DataBase Reference)
NIST Chemistry ReferencePropanoic acid, 2-[4-(2,4-dichlorophenoxy)phenoxy]-, methyl ester(51338-27-3)
EPA Substance Registry SystemDiclofop methyl (51338-27-3)

Safety Information

Hazard Codes Xn;N,N,Xn
Risk Statements 22-43-50/53
Safety Statements 24-37-60-61
RIDADR UN 3077
WGK Germany 2
RTECS UF1180000
HS Code 29189900
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Skin Sens. 1
Hazardous Substances Data51338-27-3(Hazardous Substances Data)
Toxicitydog,LD50,oral,1600mg/kg (1600mg/kg),"Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A138, Pg. 1983,

Diclofop-methyl Usage And Synthesis

Chemical PropertiesA white crystalline solid. Odorless. Can alsobe commercially available as a clear to dark brown liquidwith a typical solvent odor
UsesHerbicide.
DefinitionChEBI: Methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate is a methyl ester resulting from the formal condensation of the carboxylic acid group of 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid with methanol. It is an aromatic ether, a dichlorobenzene, a diether and a methyl ester.
General DescriptionColorless crystals. Decomposed by either strong acid or base. Used as a selective herbicide.
Air & Water ReactionsSlightly soluble in water (3 mg/l).
Reactivity ProfileA bridged diphenyl.
HazardModerately toxic by ingestion and skin contact. Low toxicity by inhalation.
Agricultural UsesHerbicide: Some uses are classified as U.S. RestrictedUse Pesticide (RUP). Diclofop-methyl is a selectivepost-emergence herbicide used to control wild oats andannual grassy weeds in grain and vegetable crops: alfalfa,carrots, celery, box, field and french beans, barley,wheat, brassicas, parsnips, peas, potatoes, rapeseed(canola), soy beans, oilseed rape, onions, sugar beets andlettuce.
Trade nameDICHLORDIPHENPROP®; HOELON®;HOELON® 3EC; HOE-GRASS®; HOEGRASS®; HOE®23408; ILOXAN®; ILLOXAN®; ONE SHOT®[C]
Potential ExposureDiclofop-methyl is a chlorophenoxy;aryloxyphenoxypropionate acid selective postemergenceherbicide used to control wild oats and annual grassy weedsin grain and vegetable crops: alfalfa, carrots, celery, box,field and French beans, barley, wheat, brassicas, parsnips,peas, potatoes, rapeseed (canola), soy beans, oilseed rape,onions, sugar beets and lettuce. Some uses are classifiedRUP
Environmental FateBiological. From the first-order biotic and abiotic rate constants of diclofop-methyl in estuarine water and sediment/water systems, the estimated biodegradation half-lives were 0.24–12.4 and 0.11–2.2 days, respectively (Walker et al., 1988).
Metabolic pathwayTwo resistant biotypes of black-grass (Peldon A1 andLincs. E1 of Alopecurus myosuroides) exhibitmoderately enhanced metabolism of 14C-diclofopmethyl. Diclofop methyl is hydrolyzed to thecorresponding propionic acid which undergoes furtherdegradation to give polar metabolites. The amounts ofthe metabolites depend on the metabolism activity ofthe individual biotypes. In wheat, three isomerichydroxylated metabolites are identified in a majormetabolic pathway after acid hydrolysis of theglucoside conjugates.
ShippingUN3345 Phenoxyacetic acid derivative pesticide,solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonousmaterials. UN3348 Phenoxyacetic acid derivative pesticide,liquid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonousmaterial. UN3077 Environmentally hazardous substances,solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneoushazardous material, Technical Name Required. Note:Commercial product may also be a liquid in a flammablecarrier.
IncompatibilitiesIncompatible with oxidizers, chloratesnitrates, peroxides, sulfuric acid, caustics, ammonia,aliphatic amines, alkanolamines, isocyanates, alkyleneoxides, and epichlorohydrin.
Waste DisposalIn accordance with40CFR165, follow recommendations for the disposal ofpesticides and pesticide containers. Containers must be disposed of properly by following package label directions orby contacting your local or federal environmental controlagency, or by contacting your regional EPA office

Diclofop-methyl Preparation Products And Raw materials

Raw materialsPropionic acid-->NITROFEN
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