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CARBETAMIDE

CAS No.
16118-49-3
Chemical Name:
CARBETAMIDE
Synonyms
561 RP;Liquide;LEGURAME;RP 11561;11,561rp;Arbetamex;leguramepm;carbetamex;carbetamid;Legurame[R]
CBNumber:
CB7717695
Molecular Formula:
C12H16N2O3
Molecular Weight:
236.27
MDL Number:
MFCD00135093
MOL File:
16118-49-3.mol
Last updated:2023-09-04 15:51:00

CARBETAMIDE Properties

Melting point >110°C
Boiling point 378.73°C (rough estimate)
Density 1.174
refractive index 1.5460 (estimate)
storage temp. 0-6°C
solubility Chloroform (Slightly), Methanol (Slightly)
pka 13.22±0.70(Predicted)
Water Solubility 3.5g/L(20 ºC)
BRN 8318291
LogP 1.520 (est)
FDA UNII A75ON2B2V7
EPA Substance Registry System Carbetamide (16118-49-3)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08,GHS09
Signal word  Danger
Hazard statements  H302-H351-H360D-H411
Precautionary statements  P201-P273-P301+P312+P330-P308+P313
Hazard Codes  Xi
WGK Germany  2
RTECS  FD8900000
HS Code  29242990
Toxicity dog,LD50,oral,900mg/kg (900mg/kg),Guide to the Chemicals Used in Crop Protection. Vol. 6, Pg. 80, 1973.

CARBETAMIDE price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 45369 Carbetamide PESTANAL 16118-49-3 250mg $94.4 2024-03-01 Buy
TRC C178028 Carbetamide 16118-49-3 250mg $120 2021-12-16 Buy
AHH MT-04527 Carbetamide 98% 16118-49-3 5g $412 2021-12-16 Buy
Product number Packaging Price Buy
45369 250mg $94.4 Buy
C178028 250mg $120 Buy
MT-04527 5g $412 Buy

CARBETAMIDE Chemical Properties,Uses,Production

Chemical Properties

Carbetamide is a colorless, crystalline powder, or solid.

Uses

Carbetamide is used in the determination of pesticides.

Definition

ChEBI: A carbamate ester obtained by the formal condensation of phenylcarbamic acid with the hydroxy group of N-ethyl-2-hydroxypropanamide.

Potential Exposure

Carbamate herbicide used to kill unwanted plants

Metabolic pathway

Photodegradation of carbetamide in solution with UV irradiation in the presence of UV ? H2O2 and ? TiO2 primarily occurs at the o- and p-positions, but not at the m-position of the phenyl ring, and the preferential photoproduct isolated is ortho-hydroxylated carbetamide. 5-Methyl-3-phenyl-oxazolidine dione is isolated only in the presence of TiO2. The cyclization may result from radical coupling with the dissolved oxygen. N-De-ethylation of the ethylcarbamoyl group and hydroxylation on the carbamoyloxy linkage occur to yield free amine of carbetamide and lactamide analogs. It is interesting to note that formulated carbetamide is phototransformed to N-ethyllactamide- 4-aminobenzoate as a major product via the rearrangement reaction similar to the Photo-Fries reaction. The degradation kinetics of carbetamide and its potential metabolites are measured at different temperatures in both unsterilized and sterilized alkaline soil.
The chemical degradation of carbetamide importantly gives N-phenyl-3-methyloxazolidine-2,5- dione which results in 2-(phenylcarbamoyloxy)- propionic acid and N-phenyl-2-hydroxypropionamide and the aniline in the soil. The purely biological degradation of this compound cannot clearly yield degradation products that are different from those by chemical degradation in non-sterilized soils.

Shipping

UN2757 Carbamate pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN 2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required

Incompatibilities

Slowly hydrolyzes in water, releasing ammonia and forming acetate salts. 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. Amides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides with strong reducing agents such as hydrideds and active metals. Amides are very weak bases (weaker than water). Mixing amides with dehydrating agents such as phosphorus pentoxide or thionyl chloride generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx). This compound is decomposed by strong base or acid.

Waste Disposal

Do not discharge into drains or sewers. Dispose of waste material as hazardous waste using a licensed disposal contractor to an approved land fill. 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.

CARBETAMIDE Preparation Products And Raw materials

Global( 95)Suppliers
Supplier Tel Email Country ProdList Advantage
Hubei Jusheng Technology Co.,Ltd.
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Alchem Pharmtech,Inc.
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TargetMol Chemicals Inc.
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Hefei TNJ Chemical Industry Co.,Ltd.
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Dayang Chem (Hangzhou) Co.,Ltd.
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LEAP CHEM CO., LTD.
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GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49999 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+undefined18621343501 product@acmec-e.com China 33349 58
Mainchem Co., Ltd. +86-0592-6210733 sale@mainchem.com China 32360 55

CARBETAMIDE Spectrum

16118-49-3(CARBETAMIDE)Related Search:

carbethamide d-(-)-1-(ethylcarbamoyl)ethylphenylcarbamate d-n-ethylacetamidecarbanilate d-n-ethyllactamidecarbanilate(ester) (2R)-N-Ethyl-2-[[(phenylamino)carbonyl]oxy]propanamide LEGURAME leguramepm n-ethyl-,carbanilate(ester),d-lactamid Carbetamex[R] D-N-Ethylactamide carbanilate ester Legurame[R] (r)-(-)-1-(ethylcarbamoyl)ethyl n-phenylcarbamate carbetamide (bsi,iso,ansi,wssa) CARBETAMID STANDARD (R)-(-)-1-(Ethylcarbamoyl)ethyl phenylcarbamate Carbetamide, (2R)-1-(Ethylamino)-1-oxopropan-2-yl phenylcarbamate Legruame P. M. Liquide RP 11561 D-N-ETHYL-2-(PHENYLCARBAMOYLOXY) PROPIONAMIDE CARBETAMIDE N-Ethyl-2-((phenylaminocarbonyl)oxy)propanamide Arbetamex (2R)-(-)-1-(Ethylcarbamoyl)ethyl phenylcarbamate Carbetamide, (2R)-(-)-1-(Ethylamino)-1-oxoprop-2-yl phenylcarbamate CARBETAMIDE PESTANAL, 250 MG ((R)-(-)-1- (1-ethylcarbamoyl)ethylester,d-(-)-carbanilicaci (phenylcarbamoyloxy)-2-n-ethylpropionamide (r)-n-ethyl-2-(((phenylamino)carbonyl)oxy)propanamide 11,561rp (R)-1-(ethylaMino)-1-oxopropan-2-yl phenylcarbaMate CarbetaMide 0 2-phenyl-carbamoyloxy-n-aethyl-propionamid carbetamex carbetamid Carbetamide Solution, 100ppm Carbetamide@1000 μg/mL in Methanol Carbetamide @100 μg/mL in MeOH Propanamide, N-ethyl-2-[[(phenylamino)carbonyl]oxy]-, (2R)- Carbetamide Solution in Methanol, 100μg/mL Carbetamide 13C6 CarbetamideQ: What is Carbetamide Q: What is the CAS Number of Carbetamide 561 RP Caswell No. 159B EPA Pesticide Chemical Code 259200 Carbetamide Standard Carbetamide Solution, 1000ppm 13C6]-Carbetamide Refametinib Impurity 9 16118-49-3