MedKoo Cat#: 581188 | Name: Thiofanox
Featured

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Thiofanox is a chemical compound used in acaricides and insecticides. Shows potential systemic & contact insecticidal properties against certain phytophagous pests.

Chemical Structure

Thiofanox
Thiofanox
CAS#39196-18-4

Theoretical Analysis

MedKoo Cat#: 581188

Name: Thiofanox

CAS#: 39196-18-4

Chemical Formula: C9H18N2O2S

Exact Mass: 218.1089

Molecular Weight: 218.32

Elemental Analysis: C, 49.52; H, 8.31; N, 12.83; O, 14.66; S, 14.69

Price and Availability

Size Price Availability Quantity
25mg USD 350.00
100mg USD 550.00
Bulk Inquiry
Buy Now
Add to Cart
Related CAS #
No Data
Synonym
Thiofanox; Benelux; Dacamox; DS-15647; HSDB 6045; Thiofanocarb;
IUPAC/Chemical Name
1-(2,2-Dimethyl-1-methylthiomethylpropylideneamino-oxy)-N-methylformamide
InChi Key
FZSVSABTBYGOQH-XFFZJAGNSA-N
InChi Code
InChI=1S/C9H18N2O2S/c1-9(2,3)7(6-14-5)11-13-8(12)10-4/h6H2,1-5H3,(H,10,12)/b11-7-
SMILES Code
O=C(O/N=C(CSC)\C(C)(C)C)NC
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 218.32 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Yamagishi Y, Nagasawa S, Iwase H, Ogra Y. Evaluation of Post-Mortem Interaction between Hemoglobin and Oxime-Type Carbamate Pesticides. Chem Res Toxicol. 2022 Jun 20;35(6):1110-1116. doi: 10.1021/acs.chemrestox.2c00092. Epub 2022 May 13. PMID: 35559618. 2: Piel C, Pouchieu C, Migault L, Béziat B, Boulanger M, Bureau M, Carles C, Grüber A, Lecluse Y, Rondeau V, Schwall X, Tual S, Lebailly P, Baldi I; AGRICAN group. Increased risk of central nervous system tumours with carbamate insecticide use in the prospective cohort AGRICAN. Int J Epidemiol. 2019 Apr 1;48(2):512-526. doi: 10.1093/ije/dyy246. PMID: 30476073. 3: Catalá-Icardo M, Meseguer-Lloret S, Torres-Cartas S. Photoinduced chemiluminescence determination of carbamate pesticides. Photochem Photobiol Sci. 2016 May 11;15(5):626-34. doi: 10.1039/c6pp00056h. Epub 2016 Apr 15. PMID: 27079156. 4: Wang L, Zhou Y, Huang X, Wang R, Lin Z, Chen Y, Wang D, Lin D, Xu D. [Determination of 51 carbamate pesticide residues in vegetables by liquid chromatography-tandem mass spectrometry based on optimization of QuEChERS sample preparation method]. Se Pu. 2013 Dec;31(12):1167-75. Chinese. doi: 10.3724/sp.j.1123.2013.05051. PMID: 24669707. 5: Saraji M, Esteki N. Analysis of carbamate pesticides in water samples using single-drop microextraction and gas chromatography-mass spectrometry. Anal Bioanal Chem. 2008 Jun;391(3):1091-100. doi: 10.1007/s00216-008-2087-8. Epub 2008 Apr 16. PMID: 18415085. 6: Rouchaud J, Thirion A, Wauters A, Van de Steene F, Benoit F, Ceustermans N, Gillet J, Marchand S, Vanparys L. Effects of fertilizer on insecticides adsorption and biodegradation in crop soils. Arch Environ Contam Toxicol. 1996 Jul;31(1):98-106. doi: 10.1007/BF00203913. PMID: 8687996. 7: Chin BH, Tallant MJ, Duane WC, Sullivan LJ. Anticholinesterase effects of carbamate insecticide thiofanox and its metabolites in rats. J Agric Food Chem. 1980 Nov-Dec;28(6):1327-30. doi: 10.1021/jf60232a029. PMID: 7451763. 8: Chin BH, Tallant MJ, Duane WC, Sullivan LJ. Metabolism of carbamate insecticide thiofanox in rats. J Agric Food Chem. 1980 Nov-Dec;28(6):1085-90. doi: 10.1021/jf60232a007. PMID: 7451737. 9: Szalkowski MB, Duane WC, Chin WT. Separation and detection of thiofanox and its metabolites by thin-layer chromatography. J Chromatogr. 1976 Dec 22;129:426-30. doi: 10.1016/s0021-9673(00)87810-3. PMID: 187610. 10: Chin WT, Duane WC, Ballee DL, Stallard DE. Mechanism of degradation of thiofanox in aqueous solutions. J Agric Food Chem. 1976 Sep-Oct;24(5):1071-3. doi: 10.1021/jf60207a020. PMID: 965596. 11: Chin WT, Duane WC, Meeks JR, Stallard DE. Changes of thiofanox residues in potatoes resulting from storage and cooking. J Agric Food Chem. 1976 Sep- Oct;24(5):1001-4. doi: 10.1021/jf60207a037. PMID: 965582. 12: Holm RE, Chin WT, Wagner DH, Stallard DE. Metabolism of thiofanox in cotton plants. J Agric Food Chem. 1975 Nov-Dec;23(6):1056-60. doi: 10.1021/jf60202a003. PMID: 1194563. 13: Chin WT, Duane WC, Szalkowski MB, Stallard DE. Gas chromatographic determination of thiofanox residues in soil, plants, and water. J Agric Food Chem. 1975 Sep-Oct;23(5):963-6. doi: 10.1021/jf60201a015. PMID: 1159201. 14: Whitten CJ, Bull DL. Fate of 3,3-dimethyl-1-(methylthio)-2-butanone O-(methylcarbamoyl)oxime(Diamond Shamrock DS-15647) in cotton plants and soil. J Agric Food Chem. 1974 Mar-Apr;22(2):234-8. doi: 10.1021/jf60192a027. PMID: 4840570.