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Phenmedipham

Phenmedipham Structure
CAS No.
13684-63-4
Chemical Name:
Phenmedipham
Synonyms
M75;Gusto;EP-452;Pistol;sn4075;Suplex;BEETUP;FENDER;ALEGRO;EP-462
CBNumber:
CB8404828
Molecular Formula:
C16H16N2O4
Molecular Weight:
300.31
MOL File:
13684-63-4.mol
MSDS File:
SDS
Modify Date:
2024/8/2 15:22:07

Phenmedipham Properties

Melting point 140-144°C
Boiling point 441.54°C (rough estimate)
Density 1.1782 (rough estimate)
refractive index 1.6240 (estimate)
Flash point 100 °C
storage temp. Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
pka 13.03±0.70(Predicted)
form Solid
color White to off-white
Water Solubility <0.1 g/100 mL at 21 ºC
BRN 2395027
LogP 3.590
CAS DataBase Reference 13684-63-4(CAS DataBase Reference)
NIST Chemistry Reference Methyl 3-m-tolylcarbamoyloxyphenylcarbamate(13684-63-4)
EPA Substance Registry System Phenmedipham (13684-63-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS09
Signal word  Warning
Hazard statements  H410
Precautionary statements  P273-P391-P501
Hazard Codes  N
Risk Statements  50/53
Safety Statements  60-61
RIDADR  UN 3077
WGK Germany  2
RTECS  FD9050000
Toxicity (96-hour) for bluegill sunfish 3.98 mg/L, rainbow trout 1.4–3.0 mg/L, Daphnia magna 3.2 mg/L (Worthing and Hance, 1991), harlequin fish 16.5 mg/L (Hartley and Kidd, 1987); acute oral LD50 of pure phenmedipham and the formulated product for rats 3,700 and 10,300 mg/kg, respectively (Ashton and Monaco, 1991).

Phenmedipham price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 36192 Phenmedipham PESTANAL?, analytical standard 13684-63-4 100MG ₹6116.13 2022-06-14 Buy
Product number Packaging Price Buy
36192 100MG ₹6116.13 Buy

Phenmedipham Chemical Properties,Uses,Production

Chemical Properties

Colorless crystalline solid, or needles; white powder. Odorless. Commercial product is available as an emulsifiable concentrate

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ChEBI: A carbamate ester that is (3-methylphenyl)carbamic acid in which the hydrogen of the hydroxy group has been replaced by a 3-[(methoxycarbonyl)amino]phenyl group.

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®

Potential Exposure

A postemergence bis-carbamate/ carbamate ester herbicide used to control of annual broadleaf weeds and grasses in sugar beets, spinach, strawberries, and sunflowers.

Environmental Fate

Soil. Phenmedipham degraded in soil forming methyl N-(3-hydroxyphenyl)-carbamate and m-aminophenol (Hartley and Kidd, 1987). Hydrolysis yields m-aminophenol (Rajagopal et al., 1989). The reported half-life in soil is approximately 20 days (Rajagopal et al., 1989) and 26 days (Worthing and Hance, 1991)
Plant. In plants, methyl N-(3-hydroxyphenyl)carbamate is the major metabolite (Hartley and Kidd, 1987)
Photolytic. Bussacchini et al. (1985) studied the photolysis (λ = 254 nm) of phenmedipham in ethanol, ethanol/water and hexane as solvents. In their proposed free radical mechanism, homolysis of the carbon-oxygen bond of the carbamate linkage ga

Shipping

UN2757 Carbamate pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material,

Incompatibilities

Decomposes .145C. Esters ith acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Carbamates are incompatible with reducing agents, strong acids, oxidizing acids, peroxides, and bases. Contact with active metals or nitrides cause the release of flammable, and potentially explosive, hydrogen gas. Releases oxides of nitrogen and carbon when heated to decomposition.

Waste Disposal

Do not discharge into drains or sewers. Dispose of waste material as hazardous waste using a licensed disposal contractor to an approved landfill. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Incineration with effluent gas scrubbing is recommended. Containers must be disposed of properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

Phenmedipham Preparation Products And Raw materials

Global( 167)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
Morden Incecide Ltd 08066085790Ext 274 Punjab, India 15 58 Inquiry
Qingdao Trust Agri Chemical Co.,Ltd +8613573296305 China 301 58 Inquiry
Hebei Jingbo New Material Technology Co., Ltd +8619931165850 China 1000 58 Inquiry
Hebei Saisier Technology Co., LTD +86-18400010335 +86-18034520335 China 1015 58 Inquiry
Hebei Longbang Technology Co., LTD +8618633929156 China 942 58 Inquiry
HebeiShuoshengImportandExportco.,Ltd +86-18532138899 +86-18532138899 China 931 58 Inquiry
Chongqing Chemdad Co., Ltd +86-023-6139-8061 +86-86-13650506873 China 39916 58 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49403 58 Inquiry

Phenmedipham Spectrum

3-methoxycarbonyl-n-(3’-methylphenyl)-carbamat 3-Methoxycarbonyl-N-(3'-methylphenyl)-carbamat Beetomax Betaflow Betalion Betamix Betanal E Betosip Carbamic acid, (3-methylphenyl)-, 3-[(methoxycarbonyl)amino]phenyl ester Carbanilic acid, m-hydroxy-, methyl ester, m-methylcarbanilate Carbanilic acid, m-hydroxy-, methyl ester, m-methylcarbanilate (ester) (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 N-[3-[(3-methylanilino)-oxomethoxy]phenyl]carbamic acid methyl ester carbanilicacid,m-hydroxy-,methylester,m-methylcarbanilate carbanilicacid,m-hydroxy,methylester,m-methylcarbanilate(ester) EP-452 Fenmedifam Goliath Gusto Headland dephend Medipham Methyl m-hydroxycarbanilate m-methylcarbanilate Methyl N-[3-[N-(3-methylphenyl)carbamoyloxy]phenyl]carbamate methyl-3-hydroxycarbanilate-3-methylcarbanilate methyl-3-m-tolycarbamoloxyphenylcarbamate methylm-hydroxycarbanilate,m-methylcarbanilate methyln-(3-(n-(3-methylphenyl)carbamoyloxy)phenyl)carbamate m-Hydroxycarbanilic acid methyl ester m-methylcarbanilate m-hydroxycarbanilicacid,methylesterm-methylcarbanilate m-hydroxycarbanilicacidmethylesterm-methylcarbanilate Phendipham phenmedipham(fenmedifam) Phenmediphame phenmediphan Pistol Pistol 400 Protrum K Protrum K SN 38584 Schering 4072 Schering-38584 SN 4075 SN-38584 sn4075 Spin-aid Suplex synbetanp Tripart beta Tripart beta 2 Vanguard METHYL 3-M-TOLYL CARBAMOYLOXY PHENYL CARBAMATE BEETUP BETANAL BETAPOST FENDER