MedKoo Cat#: 527968 | Name: Obidoxime iodide

Description:

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

Obidoxime iodide is an agricultural chemical.

Chemical Structure

Obidoxime iodide
Obidoxime iodide
CAS#4605-73-6 (iodide)

Theoretical Analysis

MedKoo Cat#: 527968

Name: Obidoxime iodide

CAS#: 4605-73-6 (iodide)

Chemical Formula: C14H16I2N4O3

Exact Mass: 541.9312

Molecular Weight: 542.12

Elemental Analysis: C, 31.02; H, 2.98; I, 46.82; N, 10.34; O, 8.85

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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Synonym
Obidoxime iodide
IUPAC/Chemical Name
1,1'-(Oxydimethylene)bis(4-formylpyridinium) diiodide dioxime
InChi Key
MLAAVDSBLFBFQX-UHFFFAOYSA-N
InChi Code
InChI=1S/C14H14N4O3.2HI/c19-15-9-13-1-5-17(6-2-13)11-21-12-18-7-3-14(4-8-18)10-16-20;;/h1-10H,11-12H2;2*1H
SMILES Code
O/N=C/C1=CC=[N+](COC[N+]2=CC=C(/C=N/O)C=C2)C=C1.[I-].[I-]
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
>3 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
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 542.12 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: Niessen KV, Seeger T, Rappenglück S, Wein T, Höfner G, Wanner KT, Thiermann H, Worek F. In vitro pharmacological characterization of the bispyridinium non-oxime compound MB327 and its 2- and 3-regioisomers. Toxicol Lett. 2018 Sep 1;293:190-197. doi: 10.1016/j.toxlet.2017.10.009. Epub 2017 Oct 10. PubMed PMID: 29024789. 2: Niessen KV, Seeger T, Tattersall JE, Timperley CM, Bird M, Green C, Thiermann H, Worek F. Affinities of bispyridinium non-oxime compounds to [(3)H]epibatidine binding sites of Torpedo californica nicotinic acetylcholine receptors depend on linker length. Chem Biol Interact. 2013 Dec 5;206(3):545-54. doi: 10.1016/j.cbi.2013.10.012. Epub 2013 Oct 21. PubMed PMID: 24157926. 3: Jun D, Kuca K, Picha J, Koleckar V, Marek J. Potency of novel oximes to reactivate sarin inhibited human cholinesterases. Drug Chem Toxicol. 2008;31(1):1-9. PubMed PMID: 18161504. 4: Zhang YH, Miyata T, Wu ZJ, Wu G, Xie LH. Hydrolysis of acetylthiocholine iodide and reactivation of phoxim-inhibited acetylcholinesterase by pralidoxime chloride, obidoxime chloride and trimedoxime. Arch Toxicol. 2007 Nov;81(11):785-92. Epub 2007 May 30. PubMed PMID: 17534602. 5: Racakova V, Hrabinova M, Jun D, Kuca K. Substituted monoquaternary oximes as reactivators of cyclosarin--and chlorpyrifos--inhibited acetylcholinesterase. Arh Hig Rada Toksikol. 2006 Dec;57(4):387-90. PubMed PMID: 17265677. 6: Worek F, Eyer P. The liberation of thiocholine from acetylthiocholine (ASCh) by pralidoxime iodide (2=PAM) and other oximes (obidoxime and diacetylmonoxime). Toxicol Lett. 2006 Dec 15;167(3):256-7; author reply 258. Epub 2006 Oct 20. PubMed PMID: 17113251. 7: Sakurada K, Ikegaya H, Ohta H, Akutsu T, Takatori T. Hydrolysis of an acetylthiocholine by pralidoxime iodide (2-PAM). Toxicol Lett. 2006 Oct 25;166(3):255-60. Epub 2006 Aug 12. PubMed PMID: 16971069. 8: Das Gupta S, Ghosh AK. Antidotal efficacy of isopropamide iodide in acute fluostigmine poisoning in mice. Pharmazie. 1985 Jul;40(7):499-500. PubMed PMID: 2864706. 9: Ramisz A, Szańkowska Z. Effect of E 600 and Toxobidin on the behavious of cholinesterases in mouse skeletal muscles in the course of experimental trichinellosis. Folia Histochem Cytochem (Krakow). 1976;14(4):321-6. PubMed PMID: 799612. 10: Shlosberg A, Egyed MN, Eilat A, Malkinson M, Preissler E. Efficacy of pralidoxime iodide and obidoxime dichloride as antidotes in diazinon-poisoned goslings. Avian Dis. 1976 Jan-Mar;20(1):162-6. PubMed PMID: 769769.