dinitrofluorobenzene

1-Fluoro-2,4-dinitrobenzene
Names
	Preferred IUPAC name 1-Fluoro-2,4-dinitrobenzene
	Other names Dinitrofluorobenzene; Sanger's reagent
Identifiers
CAS Number	70-34-8 ;
3D model (JSmol)	Interactive image;
Abbreviations	DNFB, FDNB
ChEBI	CHEBI:53049 ;
ChemSpider	21106037 ;
ECHA InfoCard	100.000.668
PubChem CID	6264;
UNII	D241E059U6 ;
	InChI InChI=1S/C6H3FN2O4/c7-5-2-1-4(8(10)11)3-6(5)9(12)13/h1-3H Key: LOTKRQAVGJMPNV-UHFFFAOYSA-N ; InChI=1/C6H3FN2O4/c7-5-2-1-4(8(10)11)3-6(5)9(12)13/h1-3H Key: LOTKRQAVGJMPNV-UHFFFAOYAZ ;
	SMILES O=[N+]([O-])c1cc(ccc1F)[N+]([O-])=O ;
Properties
Chemical formula	C6H3FN2O4
Molar mass	186.10 g·mol−1
Appearance	yellow crystals
Density	1.4718 g·cm−3 (54 °C)
Melting point	25.8 °C (78.4 °F; 298.9 K)
Boiling point	296 °C (565 °F; 569 K)
Hazards
Safety data sheet
EU classification (DSD) (outdated)	T
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

ジニトロフルオロベンゼン

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2017/08/13 11:34:25」(JST)

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1-Fluoro-2,4-dinitrobenzene (commonly called Sanger's reagent, dinitrofluorobenzene, DNFB or FDNB) is a chemical that reacts with the N-terminus of lysine in polypeptide sequencing.

Preparation

In 1936, Gottlieb presented a synthesis in which 1-chloro-2,4-dinitrobenzene reacted with potassium fluoride (KF) in nitrobenzene:^[3]

Uses

Frederick Sanger

In 1945, Frederick Sanger described its use for determining the N-terminal amino acid in polypeptide chains, in particular insulin.^[4] Sanger's initial results suggested that insulin was a smaller molecule than previously estimated (molecular weight 12,000), and that it consisted of four chains (two ending in glycine and two ending in phenylalanine), with the chains cross-linked by disulfide bonds. Sanger continued work on insulin, using dinitrofluorobenzene in combination with other techniques, eventually resulted in the complete sequence of insulin (consisting of only two chains, with a molecular weight of 6,000).^[5]

Following Sanger's initial report of the reagent, the dinitrofluorobenzene method was widely adopted for studying proteins, until it was superseded by other reagents for terminal analysis (e.g., dansyl chloride and later aminopeptidases and carboxypeptidases) and other general methods for sequence determination (e.g., Edman degradation).^[5]

Dinitrofluorobenzene reacts with the amine group in amino acids to produce dinitrophenyl-amino acids. These DNP-amino acids are moderately stable under acid hydrolysis conditions that break peptide bonds. The DNP-amino acids can then be recovered, and the identity of those amino acids can be discovered through chromatography. More recently, Sanger's reagent has also been used for the rather difficult analysis of distinguishing between the reduced and oxidized forms of glutathione and cysteine in biological systems in conjunction with HPLC. This method is so rugged that it can be performed in such complex matrices as blood or cell lysate.^[6]^[7]

Sanger's method of peptide end-group analysis: A derivatization of N-terminal end with Sanger's reagent (DNFB), B total acid hydrolysis of the dinitrophenyl peptide

References

^ ^a ^b Oxford MSDS
^ ^a ^b ^c CRC Handbook of Chemistry and Physics, 90. edition, CRC Press, Boca Raton, Florida, 2009, ISBN 978-1-4200-9084-0, Section 3, Physical Constants of Organic Compounds, p. 3-260.
^ Billroth Gottlieb, Hans (1936). "The Replacement of Chlorine by Fluorine in Organic Compounds". J. Am. Chem. Soc. 58 (3): 532–533. doi:10.1021/ja01294a502.
^ Sanger, F (1945). "The free amino groups of insulin". The Biochemical Journal. 39 (5): 507–15. PMC 1258275 . PMID 16747948. doi:10.1042/bj0390507.
^ ^a ^b Joseph Fruton, Proteins, Enzymes, Genes: The Interplay of Chemistry and Biology. New Haven: Yale University Press, 1999. p. 216.
^ Pamela K. Dominick, et al: "A new and versatile method for determination of thiolamines of biological importance", Journal of Chromatography B, 2001, 761 1-12; doi:10.1016/S0378-4347(01)00298-5.
^ Patrycja Bronowicka-Adamska, et al: "RP-HPLC method for the quantitative determination of cystathionine, cysteine, and glutathione: An application for the study of the metabolism of cysteine in human brain", Journal of Chromatography B, 2011, 879 2005-2009; doi:10.1016/j.jchromb.2011.05.026.

Literature

T. Schaefer: "The Proton Magnetic Resonance Spectrum of 1-Fluoro-2,4-dinitrobenzene", Canadian Journal of Chemistry, 1961, 40, pp. 431–433; doi:10.1139/v62-068.
B. D. Nageswara Rao: "The ¹H and ¹⁹F Resonance Spectra of 1-Fluoro-2,4-dinitrobenzene", Molecular Physics, 1964, 7 (4), pp. 307–310; doi:10.1080/00268976300101071.
A. Wilkins, R. W. H. Small: "Structure of 1-Fluoro-2,4-dinitrobenzene", Acta Crystallogr., 1991, C47, pp. 220–221; doi:10.1107/S0108270190007326.

External links

Fluorodinitrobenzene – 1-fluoro-2,4-dinitro-benzene (wikigenes.org)

UpToDate Contents

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Related Pictures

[Oxford_MSDS-1] Oxford MSDS

[CRC-2] CRC Handbook of Chemistry and Physics, 90. edition, CRC Press, Boca Raton, Florida, 2009, ISBN 978-1-4200-9084-0, Section 3, Physical Constants of Organic Compounds, p. 3-260.

[3] Billroth Gottlieb, Hans (1936). "The Replacement of Chlorine by Fluorine in Organic Compounds". J. Am. Chem. Soc. 58 (3): 532–533. doi:10.1021/ja01294a502.

[4] Sanger, F (1945). "The free amino groups of insulin". The Biochemical Journal. 39 (5): 507–15. PMC 1258275 . PMID 16747948. doi:10.1042/bj0390507.

[Fruton-5] Joseph Fruton, Proteins, Enzymes, Genes: The Interplay of Chemistry and Biology. New Haven: Yale University Press, 1999. p. 216.

[6] Pamela K. Dominick, et al: "A new and versatile method for determination of thiolamines of biological importance", Journal of Chromatography B, 2001, 761 1-12; doi:10.1016/S0378-4347(01)00298-5.

[7] Patrycja Bronowicka-Adamska, et al: "RP-HPLC method for the quantitative determination of cystathionine, cysteine, and glutathione: An application for the study of the metabolism of cysteine in human brain", Journal of Chromatography B, 2011, 879 2005-2009; doi:10.1016/j.jchromb.2011.05.026.

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