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FENOTHIOCARB

Product Name
FENOTHIOCARB
CAS No.
62850-32-2
Chemical Name
FENOTHIOCARB
Synonyms
bi-5452;PANOCON;kco-3001;PANOCON(R);FENOTHIOCARB;Fenothiocard;phenothiocarb;FENOTHIOCARB-D6;FENOTHIOCARB STANDARD;Fenothiocarb solution
CBNumber
CB5753004
Molecular Formula
C13H19NO2S
Formula Weight
253.36
MOL File
62850-32-2.mol
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FENOTHIOCARB Property

Melting point:
40.5℃
Boiling point:
155 °C
Density 
1.1414 (rough estimate)
vapor pressure 
1.6 x l0-5 Pa (23 °C)
refractive index 
1.6800 (estimate)
storage temp. 
0-6°C
Water Solubility 
30 mg l-1 (20 °C)
pka
-1.21±0.70(Predicted)
BRN 
2125738
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Safety

Hazard Codes 
Xn,N
Risk Statements 
22-50
Safety Statements 
61
RIDADR 
UN 3077 9 / PGIII
WGK Germany 
3
RTECS 
FD3825000
HS Code 
29309090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H400Very toxic to aquatic life

Precautionary statements

P273Avoid release to the environment.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
32475
Product name
Fenothiocarb
Purity
PESTANAL?, analytical standard
Packaging
25mg
Price
$261
Updated
2022/05/15
TRC
Product number
F248720
Product name
Fenothiocarb(~90%)
Packaging
100mg
Price
$435
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
PST0000382
Product name
FENOTHIOCARB
Purity
98.00%
Packaging
10ML
Price
$1617
Updated
2021/12/16
AHH
Product number
MT-51763
Product name
Fenothiocarb
Purity
98%
Packaging
10ml
Price
$500
Updated
2021/12/16
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FENOTHIOCARB Chemical Properties,Usage,Production

Uses

Fenothiocarb is an acaricide used to control the eggs and young stages of Panonychus citri, Panonychus ulmi and other Panonychus spp.

Definition

ChEBI: Fenothiocarb is an aromatic ether.

Metabolic pathway

When the red mite, applied with 14C-fenothiocarb by the contact method, metabolizes fenothiocarb, resulting in several metabolites via the primary oxidation of the N-methyl moiety. The photodegradation of fenothiocarb on silica gel plate exposed to sunlight gives rise to several degradation products. A primary photochemical reaction seems to be the oxidation of the sulfur atom to form its sulfoxide. Under greenhouse conditions, when fenothiocarb is applied to the citrus trees, the major metabolites identified in the leaves, rinds, and edible fruit are 6-O-malonyl-b-D-glucosode of N- hydroxymethyl fenothiocarb, N-formylfenothiocarb, and glucoside conjugate of phenol (not shown in the map), respectively. In soils, fenothiocarb is more rapidly degraded under upland conditions than under flooded conditions. Main degradation pathways include oxidation of the sulfur atom which results in the formation of methyl-4-phenoxybutylsulfoxide, its sulfone, and 4-phenoxybutylsulfonic acid.

Degradation

Fenothiocarb has long residual activity. It is stable to hydrolysis for 5 days (pH 5-9, 40 °C) but it is decomposed slowly by sunlight (PM). [U-14C-phenyl]Fenothiocarb was applied to the origin of silica gel TLC plates and exposed to sunlight in September or October. The plates were developed, with authentic standard compounds also applied, in two dimensions using different solvent systems. After 72 hours exposure to sunlight, 34% of parent fenothiocarb remained (DT50 45 hours). Twelve photoproducts were detected. Products that were identified are illustrated in Scheme 1 and were N-formyl-fenothiocarb (2), desmethyl-fenothiocarb (3) the bis(4-phenoxybutyl) thiolsulfinate (4), the bis(4-phenoxybutyl) thiolsulfonate (5), the sulfoxide derivative (6) and 4-phenoxybutanesulfonic acid (7). The latter two compounds were major products. The primary photochemical reaction was oxidation of sulfur to form fenothiocarb sulfoxide (6) followed by cleavage of the ester linkage and the oxidation or dimerisation of the 4-phenoxybutanesulfenic acid intermediate. The second main route of photodegradation was oxidation of the N-methyl moiety of fenothiocarb (Unai and Tomiwaza, 1986b).

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FENOTHIOCARB Suppliers

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Sichuan Kulinan Technology Co., Ltd
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11707
Advantage
57
Hangzhou Sage Chemical Co., Ltd.
Tel
+86057186818502 13588463833
Fax
Pls mail us for more information!
Email
info@sagechem.com
Country
China
ProdList
10266
Advantage
58
Nanjing Sunlida Biological Technology Co., Ltd.
Tel
025-57798810
Fax
025-57019371
Email
sales@sunlidabio.com
Country
China
ProdList
3239
Advantage
55
Shanghai HuanChuan Industry Co.,Ltd.
Tel
021-61478794
Fax
021-61478794
Email
sales@hcshhai.com
Country
China
ProdList
9793
Advantage
50
Alta Scientific Co., Ltd.
Tel
022-6537-8550 15522853686
Fax
022-2532-9655
Email
sales@altasci.com.cn
Country
China
ProdList
4511
Advantage
55
Codow Chemical Co.,Ltd.
Tel
18620099427
Fax
+86-20-62619665
Email
amy@howeipharm.com
Country
China
ProdList
17687
Advantage
55
Shandong Xiya Chemical Co., Ltd.
Tel
4009903999 13395398332
Fax
0539-6365991
Email
sales@xiyashiji.com
Country
China
ProdList
20806
Advantage
60
Raw material medicin reagent co.,Ltd
Tel
Email
sales@njromanme.com
Country
China
ProdList
4529
Advantage
58
Shanghai Vigor Biotechnology Co., Ltd.
Tel
info@vigorchem.cn 1801605789
Fax
QQ:1801605789
Country
China
ProdList
169
Advantage
58
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View Lastest Price from FENOTHIOCARB manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
Fenothiocarb 62850-32-2
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99.0%
Supply Ability
500 tons
Release date
2020-04-27
Career Henan Chemical Co
Product
FENOTHIOCARB 62850-32-2
Price
US $1.00/KG
Min. Order
1KG
Purity
95-99%
Supply Ability
1ton
Release date
2019-12-31

62850-32-2, FENOTHIOCARBRelated Search:


  • bi-5452
  • dimethylcarbamothioicacids-(4-phenoxybutyl)ester
  • dimethyl-carbamothioicacis-(4-phenoxybutyl)ester
  • kco-3001
  • phenothiocarb
  • FENOTHIOCARB
  • PANOCON
  • PANOCON(R)
  • FENOTHIOCARB STANDARD
  • s-4-phenoxybutyldimethylthiocarbamate
  • Fenothiocarb solution
  • FENOTHIOCARB-D6
  • S-(4-phenoxybutyl) dimethylthlocarbamate
  • N,N-Dimethylthiocarbamic acid S-(4-phenoxybutyl) ester
  • N,N-Dimethylthiocarbamic acid S-4-phenoxybutyl
  • Fenothiocard
  • CarbaMothioic acid, diMethyl-, S-(4-phenoxybutyl) ester
  • Fenothiocarb Solution, 1000ppm
  • N,N-Dimethylcarbamothioic acid S-(4-phenoxybutyl) ester
  • S-(4-Phenoxybutyl)-N,N-dimethylthiocarbamate
  • Fenothiocarb@1000 μg/mL in Acetone
  • Fenothiocarb@50 μg/mL in Methanol
  • Fenothiocarb@100 μg/mL in Methanol
  • Carbamothioic acid, N,N-dimethyl-, S-(4-phenoxybutyl) ester
  • Fenothiocarb Solution in Methanol, 100μg/mL
  • Avobenzone Impurity 5
  • C13497500 Fenothiocarb
  • Fenothiocarb 100 μg/ml Acetonitrile
  • Fenothiocarb in Acetone
  • Fenothiocarb in Acetonitrile
  • 62850-32-2