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Molinate

Molinate Suppliers list
Company Name: Hubei xin bonus chemical co. LTD
Tel: 86-13657291602
Email: linda@hubeijusheng.com
Products Intro: Product Name:Molinate
CAS:2212-67-1
Purity:0.99 Package:5KG;1KG
Company Name: Chongqing Chemdad Co., Ltd
Tel: +86-023-61398051 +8613650506873
Email: sales@chemdad.com
Products Intro: Product Name:Molinate
CAS:2212-67-1
Purity:0.99 Package:5KG;1KG,25KG
Company Name: CONIER CHEM AND PHARMA LIMITED
Tel: +8618523575427
Email: sales@conier.com
Products Intro: Product Name:molinate
CAS:2212-67-1
Purity:0.99 Package:1kg
Company Name: career henan chemical co
Tel: +86-0371-86658258 15093356674;
Email: factory@coreychem.com
Products Intro: Product Name:molinate
CAS:2212-67-1
Purity:98% HPLC Package:1KG;1USD
Company Name: Hangzhou MolCore BioPharmatech Co.,Ltd.
Tel: +86-057181025280; +8617767106207
Email: sales@molcore.com
Products Intro: Product Name:Molinate
CAS:2212-67-1
Purity:98% Min. Remarks:MC455068

Molinate manufacturers

  • molinate
  • molinate pictures
  • $1.00 / 1KG
  • 2020-02-04
  • CAS:2212-67-1
  • Min. Order: 1KG
  • Purity: 98% HPLC
  • Supply Ability: 10 tons
Molinate Basic information
Product Name:Molinate
Synonyms:perhydroazepin-1-carbothioate;S-Aethyl-N-hexahydro-1H-azepinthiolcarbamat;s-aethyl-n-hexahydro-1h-azepinthiolcarbamat[german];sc998;S-Ethyl 1-azepanecarbothioate;S-Ethyl 1-hexamethyleneiminothiocarbamate;S-Ethyl Hexahydroazepine-1-carbothioate;S-Ethyl N,N-hexamethylenothiocarbamate
CAS:2212-67-1
MF:C9H17NOS
MW:187.3
EINECS:218-661-0
Product Categories:ThiocarbamatesMethod Specific;2005/48/EU;Alphabetic;European Community: ISO and DIN;Herbicides;M;METI - MZPesticides&Metabolites;Alpha sort;H-MAlphabetic;Pesticides&Metabolites
Mol File:2212-67-1.mol
Molinate Structure
Molinate Chemical Properties
Melting point <25 °C
Boiling point 202°C (10 mmHg)
density 1.06
refractive index 1.5250 (estimate)
Fp 100 °C
storage temp. 0-6°C
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
pka-1.22±0.20(Predicted)
form Liquid
color Amber
Water Solubility 0.08 g/100 mL
BRN 1239196
LogP3.210
CAS DataBase Reference2212-67-1(CAS DataBase Reference)
NIST Chemistry ReferenceMolinate(2212-67-1)
EPA Substance Registry SystemMolinate (2212-67-1)
Safety Information
Hazard Codes T,N,Xn
Risk Statements 20/22-40-43-48/22-63-50/53-62
Safety Statements 36/37-46-60-61
RIDADR 2902
WGK Germany 3
RTECS CM2625000
HazardClass 6.1(b)
PackingGroup III
Hazardous Substances Data2212-67-1(Hazardous Substances Data)
ToxicityLC50 (96-hour) for bluegill sunfish 29–30 mg/L, goldfish 30 mg/L, mosquito fish 16.4 mg/L, rainbow trout 0.2–1.3 mg/L (Hartley and Kidd, 1987); acute oral LD50 of technical molinate for rats and mice 720 and 795 mg/kg, respectively (Ashton and Monaco, 1991), 501 mg/kg (RTECS, 1985).
MSDS Information
ProviderLanguage
Molinate English
Molinate Usage And Synthesis
UsesSelective herbicide used to control the germination of annual grasses and broadleaved weeds in rice crops.
DefinitionChEBI: Molinate is a member of the class of azepanes that is azepane in which the nitrogen is substituted by an (ethylsulfanyl)carbonyl group, -C(=O)SEt. A thiocarbamate herbicide not approved for use in the U.S. or European Union, it is used control grass weeds in rice paddies. It has a role as an antispermatogenic agent, a herbicide and an agrochemical. It is a member of azepanes and a monothiocarbamic ester.
General DescriptionClear liquid with aromatic odor. Non corrosive. Used as an herbicide.
Air & Water ReactionsWater soluble. Thio and dithiocarbamates slowly decompose in aqueous solution to form carbon disulfide and methylamine or other amines. Such decompositions are accelerated by acids.
Reactivity ProfileMolinate is a thiocarbamate. Flammable gases are generated by the combination of thiocarbamates and dithiocarbamates with aldehydes, nitrides, and hydrides. Thiocarbamates and dithiocarbamates are incompatible with acids, peroxides, and acid halides.
Agricultural UsesHerbicide: Molinate is a selective herbicide used on rice for the control of water grass and other weeds.
Trade nameARROSOLO®; FELAN®; HIGALNATE®; HYDRAM®; JALAN®; MALERBANE-GIAVONI-L®;ORDAM®; ORDRAM®; R-4572®; RICECO; SAKKIMOL®; STAUFFER R 4,572®; YALAN®; YULAN®
Environmental FateSoil. Hydrolyzes in soil forming ethyl mercaptan, carbon dioxide and dialkylamine (half-life approximately 2–5 weeks) (Hartley and Kidd, 1987). At recommended rates of application, the half-life of molinate in moist loam soils at 21–27°C is approximately 3 weeks (Humburg et al., 1989). Rajagopal et al. (1989) reported that under flooded conditions, molinate was hydroxylated at the 3- and 4-position with subsequent oxidation forming many compounds including molinate sulfoxide, carboxymethyl molinate, hexahydroazepine- 1-carbothioate, 4-hydroxymolinate, 4-hydroxymolinate sulfoxide, hexahydroazepine, S-methyl hexahydroazepine-1-carbothioate, 4-ketomolinate, 4-hydroxyhexahydroazepine, 4-hydroxy-N-acetyl-hexahydroazepine, carbon dioxide and bound residues.
Plant. Molinate is rapidly metabolized by plants releasing carbon dioxide and naturally occurring plant constituents (Humburg et al., 1989).
Photolytic. Molinate in a hydrogen peroxide solution (120 mM) was irradiated by UV light (l = 290 nm) at 23°C. The major photooxidation products were the two isomers of 2-oxomolinate (20% yield) and s-molinate oxide (5% yield) (Draper and Crosby, 1984).
Half-lives of 180 and 120 hours were observed using one and two equivalents of hydrogen peroxide, respectively (Draper and Crosby, 1984). Molinate has a UV absorption maximum at 225 nm and no absorption at wavelengths >290 nm. Therefore, molinate is not expected to undergo aqueous photolysis under natural sunlight (l = 290 nm). In the presence of tryptophan, a naturally occurring photosensitizer, molinate in aqueous solution photodegraded to form 1-((ethylsulfinyl)carbonyl)hexahydro-1H-azepine, S-ethyl hexahydro-2- oxo-1H-azepine-1-carbothioate and hexamethyleneimine (Soderquist et al., 1977).
Chemical/Physical. Metabolites identified in tap water were molinate sulfoxide, 3- and 4-hydroxymolinate, ketohexamethyleneimine and 4-ketomolinate (Verschueren, 1983).
Metabolic pathwayJuvenile white sturgeon and common carp are exposed to 14C-molinate in a flow-through metabolism system and oxidize molinate to form several products and hydrolyze or conjugate with glutathione (GSH), the sulfoxide, or sulfone. Both fish form a D-glucuronic acid conjugate. The higher toxicity of molinate in common carp may be due to greater bioconcentration, slower depuration, and less efficient metabolic deactivation. In the blood of common carp, molinate is oxidized by erythrocytes to the sulfoxide and possibly the sulfone, then conjugated with GSH or cysteine and cleaved to form mercapturic acid in both erythrocytes and plasma. Conjugation and possible hemoglobin carbamylation occur only after sulfoxidation of molinate. Molinate is distributed uniformly throughout the soil layers, and its degradation products are identified as 2-oxomolinate, 4-oxomolinate, molinate acid, and hexamethyleneimine. In rice plants, 4-hydroxymolinate, 2-oxomolinate, 4-oxomolinate, S-ethyl-N-carboxymethylthiocarbamate, molinate acid, and molinate alcohol are detected. By the soil microorganisms, oxidation of the S-ethyl moiety is considered to be the main pathway, and hydroxy and oxoderivatives on the azepine ring are identified.
Tag:Molinate(2212-67-1) Related Product Information
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