13684-63-4 Phenmed...

13684-63-4 Phenmedipham C16H16N2O4

13684-63-4 Phenmedipham C16H16N2O4

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1 Metric Ton

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  • Min.Order :1 Metric Ton
  • Purity: 99.5%
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Phenmedipham 13684-63-4 C16H16N2O4

Quick Details

  • Appearance:Powder
  • Application:13684-63-4
  • PackAge:Aluminium Foil Bag and Paper Drum
  • ProductionCapacity:1|Metric Ton|Day
  • Storage:1MT
  • Transportation:By Sea/Air/DHL

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Details:

 
Phenmedipham Basic information
Product Name: Phenmedipham
Synonyms: (3-methylphenyl)-carbamicaci3-((methoxycarbonyl)amino)phenylester;3-(Carbomethoxyamino)phenyl 3-methylcarbanilate;3-(carbomethoxyamino)phenyl3-methylcarbanilate;3-(Methylphenyl)carbamic acid 3-((methoxycarbonyl)amino)phenyl ester;3-(methylphenyl)carbamicacid3-((methoxycarbonyl)amino)phenylester;3-methoxycarbonyl-n-(3’-methylphenyl)-carbamat;3-Methoxycarbonyl-N-(3'-methylphenyl)-carbamat;Beetomax
CAS: 13684-63-4
MF: C16H16N2O4
MW: 300.31
EINECS: 237-199-0
Product Categories: CarbanilatePesticides&Metabolites;Alpha sort;Herbicides;N-PAlphabetic;P;PER - POLA;Pesticides&Metabolites
Mol File: 13684-63-4.mol
Phenmedipham Structure
 
Phenmedipham Chemical Properties
Melting point  140-144°C
Boiling point  441.54°C (rough estimate)
density  1.1782 (rough estimate)
refractive index  1.6240 (estimate)
Fp  100 °C
storage temp.  0-6°C
Water Solubility  <0.1 g/100 mL at 21 ºC
CAS DataBase Reference 13684-63-4(CAS DataBase Reference)
NIST Chemistry Reference Methyl 3-m-tolylcarbamoyloxyphenylcarbamate(13684-63-4)
EPA Substance Registry System Carbamic acid, (3-methylphenyl)-, 3-[(methoxycarbonyl)amino] phenyl ester(13684-63-4)
 
Safety Information
Hazard Codes  N
Risk Statements  50/53
Safety Statements  60-61
RIDADR  UN 3077
RTECS  FD9050000
Hazardous Substances Data 13684-63-4(Hazardous Substances Data)
MSDS Information
 
Phenmedipham Usage And Synthesis
Uses Phenmedipham is an carbanilate selective herbicide used post-emergence in beet crops after the emergence of most broad-leaved weeds and before they develop.
Definition ChEBI: A carbamate ester that is (3-methylphenyl)carbamic acid in which the hydrogen of the hydroxy group has been replaced by a 3-[(methoxycarbonyl)amino]phenyl group.
Uses Herbicide.
General Description Colorless crystals or white powder.
Air & Water Reactions Insoluble in water.
Reactivity Profile 3-((Methoxycarbonyl)amino)phenyl (3-methylphenyl)carbamate is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates. 3-((Methoxycarbonyl)amino)phenyl (3-methylphenyl)carbamate is incompatible with alkaline preparations.
Fire Hazard Flash point data for 3-((Methoxycarbonyl)amino)phenyl (3-methylphenyl)carbamate are not available, however 3-((Methoxycarbonyl)amino)phenyl (3-methylphenyl)carbamate is probably combustible.
Agricultural Uses Herbicide: A post-emergence herbicide for control of annual broadleaf weeds and grasses in sugar beets, spinach, strawberries, and sunflowers
Trade name AIMSAN®; BETAMIX® (phenmedipham + desmedipham); BETANAL®; CQ 1451® (phenmedipham + desmedipham + ethofumesate); EC herbicide (phenmedipham + desmedipham + ethofumesate); EP 452®; KEEPER®; KEMIFAM®; MSS HERBASAN®; NA 305® (phenmedipham + desmedipham + ethofumesate); NA 308® (phenmedipham + desmedipham + ethofumesate); POWERTWIN® (phenmedipham + ethofumesate); PROGRESS® (phenmedipham + desmedipham + ethofumesate); S-4075®; SCHERING 4072®; SN 38584®; SPINAID ®; SYNBETAN-P®; TWIN®; VANGARD®
 
Phenmedipham Preparation Products And Raw materials
Raw materials N,N-Dimethylaniline-->3-Aminophenol-->Methyl chloroformate-->m-Toluidine-->m-Tolyl isocyanate
Preparation Products the BINAP-Rh^<+^> complex

 

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