Nitrophenide
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MedKoo CAT#: 531303

CAS#: 537-91-7

Description: Nitrophenide is a bioactive chemical.


Price and Availability

Size Price Shipping out time Quantity
25g USD 220 2 Weeks
Inquire bulk and customized quantity

Pricing updated 2020-11-23. Prices are subject to change without notice.

Nitrophenide, purity > 98%, is in stock. Current shipping out time is about 2 weeks after order is received. CoA, QC data and MSDS documents are available in one week after order is received.


Chemical Structure

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Theoretical Analysis

MedKoo Cat#: 531303
Name: Nitrophenide
CAS#: 537-91-7
Chemical Formula: C12H8N2O4S2
Exact Mass: 307.9925
Molecular Weight: 308.326
Elemental Analysis: C, 46.75; H, 2.62; N, 9.09; O, 20.76; S, 20.80


Synonym: Nitrophenide

IUPAC/Chemical Name: Bis(3-nitrophenyl) disulphide

InChi Key: ODOFDWDUSSFUMN-UHFFFAOYSA-N

InChi Code: InChI=1S/C12H8N2O4S2/c15-13(16)9-3-1-5-11(7-9)19-20-12-6-2-4-10(8-12)14(17)18/h1-8H

SMILES Code: O=[N+](C1=CC(SSC2=CC=CC([N+]([O-])=O)=C2)=CC=C1)[O-]


Technical Data

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:
2934.99.9001


References

1: Wyatt TT, van Leeuwen MR, Wösten HA, Dijksterhuis J. Mannitol is essential for the development of stress-resistant ascospores in Neosartorya fischeri (Aspergillus fischeri). Fungal Genet Biol. 2014 Mar;64:11-24. doi: 10.1016/j.fgb.2013.12.010. Epub 2014 Jan 9. PubMed PMID: 24412483.

2: Zimnicka M, Wileńska B, Sekiguchi O, Uggerud E, Danikiewicz W. Reactions of nitrophenide and halonitrophenide ions with acrylonitrile and alkyl acrylates in the gas phase: addition to the carbonyl group versus Michael addition. J Mass Spectrom. 2012 Apr;47(4):425-38. doi: 10.1002/jms.2042. PubMed PMID: 22689618.

3: Danikiewicz W, Bieńkowski T, Kozłowska D, Zimnicka M. Aromatic nucleophilic substitution (SNAr) reactions of 1,2- and 1,4-halonitrobenzenes and 1,4-dinitrobenzene with carbanions in the gas phase. J Am Soc Mass Spectrom. 2007 Aug;18(8):1351-63. Epub 2007 Apr 25. PubMed PMID: 17555982.

4: Danikiewicz W, Bieńkowski T, Poddebniak D. Generation and reactions of anionic sigma-adducts of 1,3-dinitrobenzene and 1,3,5-trinitrobenzene with carbanions in a gas phase, using an electrospray ion source as the chemical reactor. J Am Soc Mass Spectrom. 2004 Jun;15(6):927-33. PubMed PMID: 15144984.

5: Allocco JJ, Nare B, Myers RW, Feiglin M, Schmatz DM, Profous-Juchelka H. Nitrophenide (Megasul) blocks Eimeria tenella development by inhibiting the mannitol cycle enzyme mannitol-1-phosphate dehydrogenase. J Parasitol. 2001 Dec;87(6):1441-8. PubMed PMID: 11780835.

6: Schmatz DM. The mannitol cycle in Eimeria. Parasitology. 1997;114 Suppl:S81-9. Review. PubMed PMID: 9309770.

7: HUANG TC, MARSHAK RR, McCAY CM. Nitrophenide and other anticoccidial studies with dogs. J Am Vet Med Assoc. 1954 Mar;124(924):212-4. PubMed PMID: 13142958.

8: GARDINER JL, FARR MM, WEHR EE. The coccidiostatic action of nitrophenide on Eimeria tenella. J Parasitol. 1952 Dec;38(6):517-24. PubMed PMID: 13023502.

9: PETERSON EH, HYMAS TA. Sulfaquinoxaline, nitrofurazone and nitrophenide in the prophylaxis of experimental Eimeria necatrix infection. Am J Vet Res. 1950 Jul;11(40):278-83. PubMed PMID: 15425753.