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MedKoo Cat#: 464451 | Name: Dialifor

Description:

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

Dialifor is an organophosphorus pesticide. It is extremely poisonous.

Chemical Structure

Dialifor
Dialifor
CAS#10311-84-9

Theoretical Analysis

MedKoo Cat#: 464451

Name: Dialifor

CAS#: 10311-84-9

Chemical Formula: C14H17ClNO4PS2

Exact Mass: 393.0025

Molecular Weight: 393.84

Elemental Analysis: C, 42.70; H, 4.35; Cl, 9.00; N, 3.56; O, 16.25; P, 7.86; S, 16.28

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
Dialifor; Dialiphor; Dialiphos; Torak;
IUPAC/Chemical Name
S-(2-chloro-1-(1,3-dioxoisoindolin-2-yl)ethyl) O,O-diethyl phosphorodithioate
InChi Key
MUMQYXACQUZOFP-UHFFFAOYSA-N
InChi Code
InChI=1S/C14H17ClNO4PS2/c1-3-19-21(22,20-4-2)23-12(9-15)16-13(17)10-7-5-6-8-11(10)14(16)18/h5-8,12H,3-4,9H2,1-2H3
SMILES Code
CCOP(OCC)(SC(N1C(c2c(C1=O)cccc2)=O)CCl)=S
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
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
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 393.84 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: Vassetti D, Pagliai M, Procacci P. Assessment of GAFF2 and OPLS-AA General Force Fields in Combination with the Water Models TIP3P, SPCE, and OPC3 for the Solvation Free Energy of Druglike Organic Molecules. J Chem Theory Comput. 2019 Mar 12;15(3):1983-1995. doi: 10.1021/acs.jctc.8b01039. Epub 2019 Feb 14. PMID: 30694667. 2: Ellington JJ, Evans JJ, Prickett KB, Champion WL Jr. High-performance liquid chromatographic separation of the enantiomers of organophosphorus pesticides on polysaccharide chiral stationary phases. J Chromatogr A. 2001 Sep 14;928(2):145-54. doi: 10.1016/s0021-9673(01)01138-4. PMID: 11587332. 3: Kalafatić M, Znidarić D, Lui A, Wrischer M. Effect of insecticides (Dimiline WP 25, Torak EC 24 and Gamacide 20) on hydra (Hydra vulgaris Pallas). Int J Dev Biol. 1991 Sep;35(3):335-40. PMID: 1726048. 4: Besser R, Vogt T, Gutmann L. Pancuronium improves the neuromuscular transmission defect of human organophosphate intoxication. Neurology. 1990 Aug;40(8):1275-7. doi: 10.1212/wnl.40.8.1275. PMID: 2166248. 5: Gaines TB, Linder RE. Acute toxicity of pesticides in adult and weanling rats. Fundam Appl Toxicol. 1986 Aug;7(2):299-308. doi: 10.1016/0272-0590(86)90160-0. PMID: 3758548. 6: Nigg HN, Stamper JH. Comparative disappearance of dioxathion, malathion, oxydemetonmethyl and dialifor from Florida citrus leaf and fruit surfaces. Arch Environ Contam Toxicol. 1981 Jul;10(4):497-504. doi: 10.1007/BF01055445. PMID: 7259310. 7: Winterlin W, Walker G, Hall G, McFarland J, Mourer C. Environmental fate of dialifor and formation of its oxygen analogue following application on grape vines in the San Joaquin Valley, California. J Agric Food Chem. 1980 Nov- Dec;28(6):1078-83. doi: 10.1021/jf60232a006. PMID: 7451736. 8: Kawar NS, Iwata Y, Düsch ME, Gunther FA. Behavior of dialifor, dimethoate, and methidathion in artificially fortified grape juice processed into wine. J Environ Sci Health B. 1979;14(5):505-13. doi: 10.1080/03601237909372146. PMID: 469174. 9: Peoples SA, Maddy KT. Organophosphate pesticide poisoning. West J Med. 1978 Oct;129(4):273-7. PMID: 716389; PMCID: PMC1238349. 10: Winterlin W, Kilgore W, Mourer C, Mull R, Walker G, Knaak J, Maddy K. Dislodgable residues of dialifor and phosalone and their oxygen analogs following a reported worker-injury incident in the San Joaquin Valley, California. Bull Environ Contam Toxicol. 1978 Aug;20(2):255-60. doi: 10.1007/BF01683517. PMID: 698434. 11: Knaak JB, Peoples SA, Jackson TJ, Fredrickson AS, Enos R, Maddy KT, Bailey JB, Düsch ME, Gunther FA, Winterlin WL. Reentry problems involving the use of dialifor on grapes in the San Joaquin Valley of California. Arch Environ Contam Toxicol. 1978;7(4):465-81. doi: 10.1007/BF02332072. PMID: 755446. 12: Westlake WE, Düsch ME, Gunther FA, Jeppson LR. Persistence of O,O-diethyl S-(2-chloro-1-phthalimidoethyl)-phosphorodithioate (Torak) on and in lemons, oranges, and dried citrus pulp cattle feed, and toxicity of the residues to mites. J Agric Food Chem. 1971 Nov-Dec;19(6):1191-5. doi: 10.1021/jf60178a049. PMID: 5132648.

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