Methiocarb-d3
- Product Name
- Methiocarb-d3
- CAS No.
- 1581694-94-1
- Chemical Name
- Methiocarb-d3
- Synonyms
- Methicarb-D3;Methiocarb-d3;D3-Methiocarb;[2H3]-Methiocarb;Mercaptodimethur-d3;Methiocarb-(N-methyl-d3);*Crisaborole Impurity 75;YFBPRJGDJKVWAH-HPRDVNIFSA-N;Methiocarb-d3 in acetonitrile;C15020501 Methiocarb D3 (N-methyLD3)
- CBNumber
- CB32751127
- Molecular Formula
- C11H15NO2S
- Formula Weight
- 225.31
- MOL File
- 1581694-94-1.mol
Methiocarb-d3 Property
- storage temp.
- Store at -20°C
- solubility
- DMF: 20 mg/ml,DMSO: 20 mg/ml,DMSO:PBS (pH 7.2) (1:1): 0.5 mg/ml,Ethanol: 10 mg/ml
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H300Fatal if swallowed
H410Very toxic to aquatic life with long lasting effects
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P273Avoid release to the environment.
P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P391Collect spillage. Hazardous to the aquatic environment
P405Store locked up.
N-Bromosuccinimide Price
- Product number
- 32300
- Product name
- Methiocarb-(N-methyl-d3)
- Purity
- PESTANAL?, analytical standard
- Packaging
- 10mg
- Price
- $199
- Updated
- 2022/05/15
- Product number
- 27776
- Product name
- Methiocarb-d3
- Packaging
- 1mg
- Price
- $152
- Updated
- 2024/03/01
- Product number
- 27776
- Product name
- Methiocarb-d3
- Purity
- ≥99% deuterated forms (d<sub>1</sub>-d<sub>3</sub>)
- Packaging
- 5 mg
- Price
- $608
- Updated
- 2024/03/01
- Product number
- M225242
- Product name
- Methiocarb-d3
- Packaging
- 10mg
- Price
- $1455
- Updated
- 2021/12/16
- Product number
- 164875
- Product name
- Methiocarb-d3
- Packaging
- 2.5mg
- Price
- $460
- Updated
- 2021/12/16
Methiocarb-d3 Chemical Properties,Usage,Production
Description
Methiocarb-d3 is intended for use as an internal standard for the quantification of methiocarb by GC- or LC-MS. Methiocarb is a carbamate pesticide with insecticidal, molluscicidal, acaricidal, and bird repellant properties. It inhibits acetylcholinesterase (AChE) activity and is toxic to the western flower thrip (F. occidentalis; IC50 = 2.1 μM; LC50 = 3.26 ppm). Methiocarb is also toxic to the land snail M. obstructa (LD50 = 27.4 μg/snail) and the citrus mite A. pelekassi, inducing 94% mortality when used at a concentration of 0.5 ppm. It reduces the seasonal percentages of cotton bolls infested with pink bollworm (P. gossypiella) to 4%, compared with 65% infestation in untreated controls, when applied to cotton fields at a concentration of 1.86 lb/acre. Methiocarb reduces damage to grapes by song birds when applied to vineyards at a concentration of 2.5 lbs AI per 100 gal water per acre. It is an estrogen receptor α (ERα) and ERβ agonist (EC20s = 19.87 and 20.24 μM, respectively) and an androgen receptor antagonist (IC50 = 13.89 μM) in cell-based reporter assays. It is toxic to juvenile rainbow trout (O. mykiss) and guppies (P. reticulata) with LC50 values of 0.8 and 1.48 mg/L, respectively, at 48 hours of exposure. Formulations containing methiocarb have been used in the agricultural control of pests.
Uses
Isotope labelled Methiocarb acts as a pesticide which is used in the protection of crops from insects and fungus.
References
[1] JENSEN S E. Acetylcholinesterase Activity Associated with Methiocarb Resistance in a Strain of Western Flower Thrips,Frankliniella occidentalis(Pergande)[J]. Pesticide Biochemistry and Physiology, 1998, 61 3: Pages 191-200. DOI: 10.1006/pest.1998.2359
[2] H. HUSSEIN. Molluscicidal activity of Pergularia tomentosa (L.), methomyl and methiocarb, against land snails[J]. International Journal of Pest Management, 1999, 45 1: 211-213. DOI: 10.1080/096708799227815
[3] P. NORMAN C C D K Reed. Pesticides Screened Against Two Rust Mites of Citrus[J]. Journal of Economic Entomology, 1967, 63 1: 1409-1412. DOI: 10.1093/jee/63.5.1409
[4] SATOKO TANGE . In vitro metabolism of methiocarb and carbaryl in rats, and its effect on their estrogenic and antiandrogenic activities[J]. Environmental toxicology and pharmacology, 2016, 41: Pages 289-297. DOI: 10.1016/j.etap.2015.08.014
[5] De Souza, F.I., Zumiotti, A.V., and Da Silva, C.F. Neuregulins 1-α and 1-β on the regeneration the peripheral nerves[J]. Acta Ortop Bras.
Methiocarb-d3 Preparation Products And Raw materials
Raw materials
Preparation Products
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