N,N-Diphenylamine | CAS#: 122-39-4 | fungicide

MedKoo Cat#: 582020 | Name: N,N-Diphenylamine

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Description:

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

N,N-Diphenylamine is an aromatic amine containing two phenyl substituents. It has been used as a fungicide for the treatment of superficial scald in apples and pears, but is no longer approved for this purpose within the European Union. It has a role as a carotogenesis inhibitor, an antioxidant, an EC 1.3.99.29 [phytoene desaturase (zeta-carotene-forming)] inhibitor and an antifungal agrochemical. It is an aromatic amine, a secondary amino compound and a bridged diphenyl fungicide.

Chemical Structure

N,N-Diphenylamine

CAS#122-39-4

Theoretical Analysis

MedKoo Cat#: 582020

Name: N,N-Diphenylamine

CAS#: 122-39-4

Chemical Formula:

Exact Mass:

Molecular Weight:

Elemental Analysis:

Price and Availability

Size	Price	Availability	Quantity
100g	USD 203.00
500g	USD 330.00
2500g	USD 590.00

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Related CAS #

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Synonym

N,N-Diphenylamine; N-Phenylbenzenamine; Anilinobenzene; NSC 215210; N-Fenylanilin; Phenylaniline; Scaldip; Diphenylamine; Anilinobenzene; Benzenamine, N-phenyl-.

IUPAC/Chemical Name

diphenylamine

InChi Key

DMBHHRLKUKUOEG-UHFFFAOYSA-N

InChi Code

InChI=1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H

SMILES Code

c1(Nc2ccccc2)ccccc1

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

More Info

Instruction

View handling instruction

Preparing Stock Solutions

The following data is based on the product molecular weight 0.00 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.

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: Küçüköz B, Sevinç G, Yildiz E, Karatay A, Zhong F, Yılmaz H, Tutel Y, Hayvalı M, Zhao J, Yaglioglu HG. Enhancement of two photon absorption properties and intersystem crossing by charge transfer in pentaaryl boron-dipyrromethene (BODIPY) derivatives. Phys Chem Chem Phys. 2016 May 11;18(19):13546-53. doi: 10.1039/c6cp01266c. PubMed PMID: 27138347. 2: Chen G, Li SY, Malik HT, Ma YG, Xu H, Sun LK. Organic two-photon nanoparticles modulate reactive oxygen species, intracellular calcium concentration, and mitochondrial membrane potential during apoptosis of human gastric carcinoma SGC-7901 cells. Biotechnol Lett. 2016 Aug;38(8):1269-76. doi: 10.1007/s10529-016-2105-4. Epub 2016 Apr 11. PubMed PMID: 27067355. 3: Bandyopadhyay S, Métivier R, Pallavi P, Preis E, Nakatani K, Landfester K, Patra A, Scherf U. Conjugated Polymer Nanoparticle-Triplet Emitter Hybrids in Aqueous Dispersion: Fabrication and Fluorescence Quenching Behavior. Macromol Rapid Commun. 2016 Feb;37(3):271-7. doi: 10.1002/marc.201500618. Epub 2015 Dec 14. PubMed PMID: 26663576. 4: Sreenivasu M, Suzuki A, Adachi M, Kumar CV, Srikanth B, Rajendar S, Rambabu D, Kumar RS, Mallesham P, Rao NV, Kumar MS, Reddy PY. Synthesis and characterization of donor-π-acceptor-based porphyrin sensitizers: potential application of dye-sensitized solar cells. Chemistry. 2014 Oct 20;20(43):14074-83. doi: 10.1002/chem.201403660. Epub 2014 Sep 10. PubMed PMID: 25210010. 5: Kitchen JA, Olguín J, Kulmaczewski R, White NG, Milway VA, Jameson GN, Tallon JL, Brooker S. Effect of N4-substituent choice on spin crossover in dinuclear iron(II) complexes of bis-terdentate 1,2,4-triazole-based ligands. Inorg Chem. 2013 Oct 7;52(19):11185-99. doi: 10.1021/ic4014416. Epub 2013 Sep 20. PubMed PMID: 24050255. 6: Rabe T, Görrn P, Lehnhardt M, Tilgner M, Riedl T, Kowalsky W. Highly sensitive determination of the polaron-induced optical absorption of organic charge-transport materials. Phys Rev Lett. 2009 Apr 3;102(13):137401. Epub 2009 Mar 30. PubMed PMID: 19392402. 7: Liu J, Mao Y, Huang M, Gu Y, Zhang W. Three-photon absorption cross-section enhancement in two symmetrical fluorene-based molecules. J Phys Chem A. 2007 Sep 20;111(37):9013-8. Epub 2007 Aug 28. PubMed PMID: 17722895. 8: Piech K, Bally T, Sikora A, Marcinek A. Mechanistic aspects of the oxidative and reductive fragmentation of N-nitrosoamines: a new method for generating nitrenium cations, amide anions, and aminyl radicals. J Am Chem Soc. 2007 Mar 21;129(11):3211-7. Epub 2007 Mar 1. PubMed PMID: 17328546. 9: Krieg R, Halbhuber KJ, Oehring H. Novel chromogenic substrates with metal chelating properties for the histochemical detection of peroxidasic activity, derived from 3-amino-9-ethylcarbazole (AEC) and 3,6-diamino-9-ethylcarbazole. Cell Mol Biol (Noisy-le-grand). 2000 Nov;46(7):1191-212. PubMed PMID: 11075949. 10: Steffenrud S, Borgeat P, Bertrand MJ. Syntheses and comparison of three reagents for allyldimethylsilylation of prostaglandins and steroids: a gas chromatographic method. J Chromatogr Sci. 1989 Sep;27(9):545-8. PubMed PMID: 2808642. 11: Wangemann P, Wittner M, Di Stefano A, Englert HC, Lang HJ, Schlatter E, Greger R. Cl(-)-channel blockers in the thick ascending limb of the loop of Henle. Structure activity relationship. Pflugers Arch. 1986;407 Suppl 2:S128-41. PubMed PMID: 2434915. 12: Araki A, Muramatsu M, Matsushima T. Comparison of mutagenicities of N-nitrosamines on Salmonella typhimurium TA100 and Escherichia coli WP2 uvrA/pKM101 using rat and hamster liver s9. Gan. 1984 Jan;75(1):8-16. PubMed PMID: 6373472. 13: Wakabayashi K, Nagao M, Kawachi T, Sugimura T. Mechanism of appearance of mutagenicity of N-nitrosodiphenylamine with norharman. IARC Sci Publ. 1982;(41):695-707. PubMed PMID: 7141576.