Mercaptodimetur (ISO)

Mercaptodimethur Struktur
2032-65-7
CAS-Nr.
2032-65-7
Bezeichnung:
Mercaptodimetur (ISO)
Englisch Name:
Mercaptodimethur
Synonyma:
METHIOCARB;MXMC;Club;OMS93;H 321;Draza;b37344;certan;dcr736;Esurol
CBNumber:
CB1254073
Summenformel:
C11H15NO2S
Molgewicht:
225.31
MOL-Datei:
2032-65-7.mol

Mercaptodimetur (ISO) Eigenschaften

Schmelzpunkt:
119°C
Dichte
1.1838 (rough estimate)
Dampfdruck
1.5 x 10-5 Pa (20 °C)
Brechungsindex
1.4790 (estimate)
storage temp. 
0-6°C
Löslichkeit
DMF: 20 mg/ml,DMSO: 20 mg/ml,DMSO:PBS (pH 7.2) (1:1): 0.5 mg/ml,Ethanol: 10 mg/ml
Aggregatzustand
Crystalline Solid
Siedepunkt:
310.7±42.0 °C(Predicted)
pka
12.16±0.46(Predicted)
Farbe
White
Wasserlöslichkeit
Insoluble
BRN 
1881431
Stabilität:
Light Sensitive
CAS Datenbank
2032-65-7(CAS DataBase Reference)
NIST chemische Informationen
4-Methylthio-3,5-xylyl methylcarbamate(2032-65-7)
EPA chemische Informationen
Methiocarb (2032-65-7)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher T;N,N,T
R-Sätze: 25-50/53
S-Sätze: 22-37-45-60-61
RIDADR  UN 2811/2757
WGK Germany  3
RTECS-Nr. FC5775000
HazardClass  6.1(a)
PackingGroup  II
Giftige Stoffe Daten 2032-65-7(Hazardous Substances Data)
Toxizität LD50 in male, female rats (mg/kg): 70, 60 orally (Gaines)
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H300 Lebensgefahr bei Verschlucken. Akute Toxizität oral Kategorie 2 Achtung GHS hazard pictogramssrc="/GHS06.jpg" width="20" height="20" /> P264, P270, P301+P310, P321, P330,P405, P501
H410 Sehr giftig für Wasserorganismen mit langfristiger Wirkung. Langfristig (chronisch) gewässergefährdend Kategorie 1 Warnung GHS hazard pictogramssrc="/GHS09.jpg" width="20" height="20" /> P273, P391, P501
Sicherheit
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P273 Freisetzung in die Umwelt vermeiden.
P301+P310 BEI VERSCHLUCKEN: Sofort GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P391 Verschüttete Mengen aufnehmen.
P405 Unter Verschluss aufbewahren.

Mercaptodimetur (ISO) Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R25:Giftig beim Verschlucken.
R50/53:Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.

S-Sätze Betriebsanweisung:

S22:Staub nicht einatmen.
S37:Geeignete Schutzhandschuhe tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S60:Dieses Produkt und sein Behälter sind als gefährlicher Abfall zu entsorgen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.

Beschreibung

Methiocarb was originally developed by Bayer as an insecticide. The bird-repellent properties of the compound were quickly recognized, however, and a number of applications for bird damage management followed (42).
Methiocarb is a secondary repellent, and repellency occurs through aversive conditioning, by which birds that feed on treated food become sick and associate either the food or characteristics of the food with the discomfort (21). As a result, affected birds learn to avoid that food item. Often the avoidance response is locationdependent. For example, common ravens (Corvus corax) that learn not to eat eggs at one site will still feed on eggs at a different location (43).

Chemische Eigenschaften

Methiocarb is a colorless crystalline powder.

Verwenden

Insecticide; molluscicide; bird repellent.

Definition

ChEBI: A carbamate ester obtained by the formal condensation of the phenolic group of 3,5-dimethyl-4-(methylsulfanyl)phenol with the carboxy group of methylcarbamic acid.

Allgemeine Beschreibung

White crystalline powder with a mild odor. Used as an insecticide and immobilizing agent for birds, acaricide and molluscicide.

Reaktivität anzeigen

Mercaptodimethur 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.

Health Hazard

As a carbamate insecticide, Mercaptodimethur is a reversible cholinesterase inhibitor and acts on the nervous system. It is classified as very toxic, and the probable oral lethal dose for humans is 50-500 mg/kg or between 1 teaspoon and 1 ounce for a 150 lb. adult.

Brandgefahr

When heated to decomposition, Mercaptodimethur emits very toxic fumes of nitrogen and sulfur oxides.

Landwirtschaftliche Anwendung

Acaricide, Molluscicide, Insecticide: Used to control slugs and snails, soil insects and spider mites in pome fruit, stone fruit, hops, strawberries, potatoes, beets, maize, vegetables and ornamentals. Also used as seed treatment to control fruit flies on maize and bird repellant on berries and cherries. Methiocarb producers deleted all food uses from their product labels between 1989-92. It is A U.S. EPA restricted Use Pesticide (RUP) except for residential application.

Handelsname

AI3-25726®; ALCO SLUB”M[C]; B 37344®; BAY 5024®; BAY 9026®; BAY 37344®; BAYER 37344®; DCR 736®; DRAZA®; DRAZA G MICROPELLETS®; H 321®; MESUROL®; METHIOCARBE®; OMS- 93®; PBI SLUG GARD®; PROVADA®; SD 9228®; SLUG-GETA®[C]

Kontakt-Allergie

Methiocarb is an insecticide or molluscicide with a cholinesterase inhibiting effect. A case of contact dermatitis was reported in a carnation grower.

Pharmakologie

Methiocarb is a carbamate, and its mode of action is via the inhibition of acetylcholinesterase at synapses in the nervous system. Unlike many cholinesterase-inhibiting compounds, however, the effects of methiocarb are rapidly reversible, and the animal experiences only transitory disruption.

Sicherheitsprofil

Poison by ingestion, skin contact, and intraperitoneal routes. Used as an insecticide, molluscicide, and bird repellent. When heated to decomposition it emits very toxic fumes of NOx and SOx. See also ESTERS and CARBAMATES.

mögliche Exposition

A potential danger to those involved in the manufacture, formulation, and application of this nonsystemic acaricide and insecticide.

Environmental Fate

Soil. Methiocarb was oxidized, probably by singlet oxygen, to the corresponding sulfoxide and trace amounts (<5% yield) of sulfone when sorbed on soil and exposed to sunlight. The photosensitized oxidation was faster in soils containing the lowest organic carbon content (Gohre and Miller, 1986).
Plant. On and/or in bean plants, the methylthio group is rapidly oxidized to the sulfoxide and sulfone (Abdel-Wahab et al., 1966) followed by hydrolysis yielding the corresponding thiophenol, methylsulfoxide phenol and methylsulphonyl phenol (Har
Photolytic. When methiocarb in ethanol was irradiated by UV light, only a few unidentified cholinesterase inhibitors were formed (Crosby et al., 1965).
Chemical/Physical. Emits toxic fumes of nitrogen and sulfur oxides when heated to decomposition (Sax and Lewis, 1987).

Stoffwechselwegen

Methiocarb is oxidised to a sulfoxide and a sulfone in biological media. The resulting two carbamate esters and the parent compound are hydrolysed in soils and plants to the corresponding phenols. Hydroxylation of the N-methyl group on the carbamate function occurs in mammalian preparations in vitro.

Versand/Shipping

UN2757 Carbamate pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required

Waste disposal

In accordance with 40CFR 165 recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform to EPA regulations governing storage, transportation, treatment, and waste disposal. Remove material with contaminated soil and place in impervious containers. May be incinerated in a pesticide incinerator at the specified temperature/dwell-time combination. Any liquids, sludges, or solid residues generated should be disposed of in accordance with all applicable federal, state, and local pollution control requirements. If appropriate incineration facilities are not available, material may be buried in a chemical waste landfill. May be amenable to biological treatment at a municipal sewage treatment plant. (Sax/DPIMR).

Mercaptodimetur (ISO) Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Mercaptodimetur (ISO) Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 104)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hubei Jusheng Technology Co.,Ltd.
18871490254
linda@hubeijusheng.com CHINA 28172 58
Xiamen AmoyChem Co., Ltd
+86-86-5926051114 +8618959220845
sales@amoychem.com China 6383 58
Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873
sales@chemdad.com China 39894 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427
sales@conier.com China 49374 58
career henan chemical co
+86-0371-86658258 +8613203830695
factory@coreychem.com China 29811 58
Hebei Mojin Biotechnology Co., Ltd
+86 13288715578 +8613288715578
sales@hbmojin.com China 12840 58
SIMAGCHEM CORP
+86-13806087780
sale@simagchem.com China 17365 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000
marketing@targetmol.com United States 32165 58
LEAP CHEM CO., LTD.
+86-852-30606658
market18@leapchem.com China 24727 58
Hebei Weibang Biotechnology Co., Ltd
+8617732866630
bess@weibangbio.com China 18154 58

2032-65-7(Mercaptodimetur (ISO))Verwandte Suche:


  • OMS93
  • Phenol,3,5-diMethyl-4-(Methylthio)-, 1-(N-MethylcarbaMate)
  • MXMC
  • 3,5-dimethyl-4-methylthiophenyl N-methylcarbamate,mercaptodimethur (ISO),methiocarb
  • (3,5-dimethyl-4-methylsulfanyl-phenyl) N-methylcarbamate
  • (3,5-dimethyl-4-methylsulfanylphenyl) N-methylcarbamate
  • N-methylcarbamic acid [3,5-dimethyl-4-(methylthio)phenyl] ester
  • Methiocarb 1g [2032-65-7]
  • 3,5-Dimethyl-4-(methylsulfanyl)phenyl methylcarbamate
  • 3,5-dimethyl-4-(methylthio)-phenomethylcarbamate
  • 3,5-dimethyl-4-methylmercaptophenyl-n-methyl-carbamate
  • 3,5-Dimethyl-4-methylthiophenyl N-methylcarbamate
  • 3,5-Dimethyl-4-methyl-thiophenyl-N-carbamat
  • 3,5-dimethyl-4-methylthiophenyln-methylcarbamate
  • 3,5-Xylenol, 4-(methylthio)-, methylcarbamate
  • 4-(Methylthio)-3,5-dimethylphenyl methylcarbamate
  • 4-Methylmercapto-3,5-dimethylphenyl N-methylcarbamate
  • 4-methylmercapto-3,5-dimethylphenyln-methylcarbamate
  • 4-Methylmercapto-3,5-xylyl methylcarbamate
  • 4-methylmercapto-3,5-xylylmethylcarbamate
  • 3,5-Dimethyl-4-(methylthio)phenol methylcarbamate
  • 3,5-DIMETHYL-4-[METHYLTHIO]PHENYL METHYLCARBAMATE
  • Mesurol
  • MESUROL(R)
  • MERCAPTODIMETHUR
  • Methylcarbamic acid 4-(methylthio)-3,5-xylyl ester
  • BAYER 37344
  • ENT25726
  • H 321
  • METHIOCARB, 1GM, NEAT
  • MERCAPTODIMETHUR PESTANAL
  • Metmercapturon[R]
  • mercaptodimethur (iso,f,frg)
  • methiocarb (bsi,can,nz,esa,iso)
  • Methiocarb(Mercaptodimethur)
  • mercaptodimethur (ISO) methiocarb 3,5-dimethyl-4-methylthiophenyl N-methylcarbamate
  • Miechongwei
  • 4-methylthio-3,5-dimethylphenylmethylcarbamate
  • 5-xylenol,4-(methylthio)-methylcarbamate
  • B 37344
  • b37344
  • BAY 37344
  • BAY 5024
  • BAY 9026
  • bay37344
  • bay5024
  • bay9026
  • Borderland black
  • Carbamic acid, 3,5-dimethyl-4-methylthiophenyl ester, N-methyl
  • Carbamic acid, methyl-, 3,5-dimethyl-4-(methylthio)phenyl ester
  • Carbamic acid, methyl-, 4-(methylthio)-3,5-xylyl ester
  • Carbamic acid, N-methyl-, 4-(methylthio)-3,5-xylyl ester
  • carbamicacid,methyl-,3,5-dimethyl-4-(methylthio)phenylester
  • carbamicacid,methyl-,4-(methylthio)-3,5-xylylester
  • carbamicacid,n-methyl-,4-(methylthio)-3,5-xylylester
  • carbamicacid,N-methyl-,4-methylthio-3,5-xylylester
  • certan
  • Club
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