Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1919 1
1945 2
1946 2
1947 6
1948 5
1949 3
1950 3
1951 3
1952 1
1953 1
1954 4
1955 4
1956 2
1957 6
1958 4
1959 2
1960 2
1961 8
1962 6
1963 2
1964 5
1966 1
1967 2
1969 2
1972 2
1973 1
1974 2
1975 5
1976 8
1977 4
1978 10
1979 8
1980 6
1981 15
1982 11
1983 7
1984 10
1985 16
1986 15
1987 12
1988 7
1989 3
1990 8
1991 11
1992 7
1993 8
1994 7
1995 7
1996 2
1997 8
1998 3
1999 6
2000 9
2001 11
2002 6
2003 9
2004 4
2005 5
2006 10
2007 18
2008 20
2009 15
2010 15
2011 19
2012 17
2013 8
2014 13
2015 15
2016 20
2017 15
2018 12
2019 7
2020 13
2021 12
Text availability
Article attribute
Article type
Publication date

Search Results

521 results
Results by year
Filters applied: . Clear all
Page 1
HC Yellow No. 4.
Becker LC. Becker LC. Int J Toxicol. 2017 Sep/Oct;36(5_suppl2):34S. doi: 10.1177/1091581817717644. Int J Toxicol. 2017. PMID: 29025340 No abstract available.
2,4,6-Trinitro-N-[4-(phenyl-diazen-yl)phen-yl]aniline.
Smith G, Wermuth UD. Smith G, et al. Acta Crystallogr Sect E Struct Rep Online. 2011 Apr 1;67(Pt 4):o948. doi: 10.1107/S160053681101004X. Epub 2011 Mar 23. Acta Crystallogr Sect E Struct Rep Online. 2011. PMID: 21754214 Free PMC article.
The title compound, C(18)H(12)N(6)O(6), was prepared from the reaction of 4-(phenyl-diazen-yl)aniline (aniline yellow) with picryl-sulfonic acid. The dihedral angle formed by the two benzene rings of the diphenyl-diazenyl ring system is 6.55 (13) and that for …
The title compound, C(18)H(12)N(6)O(6), was prepared from the reaction of 4-(phenyl-diazen-yl)aniline (aniline yellow) …
Aniline--a 'historical' contact allergen? Current data from the IVDK and review of the literature.
Uter W, Stropp G, Schnuch A, Lessmann H. Uter W, et al. Ann Occup Hyg. 2007 Mar;51(2):219-26. doi: 10.1093/annhyg/mel076. Epub 2006 Nov 28. Ann Occup Hyg. 2007. PMID: 17135213 Review.
OBJECTIVES: To assess whether aniline should be regarded as potential cause of contact allergy (CA). ...RESULTS: In the above period, 25 of the 1119 patients patch tested with aniline had positive (allergic) reactions; in 24 of these 25 patients, CA to p-phen …
OBJECTIVES: To assess whether aniline should be regarded as potential cause of contact allergy (CA). ...RESULTS: In the above period, …
Proton transfer versus nontransfer in compounds of the diazo-dye precursor 4-(phenyldiazenyl)aniline (aniline yellow) with strong organic acids: the 5-sulfosalicylate and the dichroic benzenesulfonate salts, and the 1:2 adduct with 3,5-dinitrobenzoic acid.
Smith G, Wermuth UD, Young DJ, White JM. Smith G, et al. Acta Crystallogr C. 2009 Oct;65(Pt 10):o543-8. doi: 10.1107/S0108270109036622. Epub 2009 Sep 30. Acta Crystallogr C. 2009. PMID: 19805891
The structures of two 1:1 proton-transfer red-black dye compounds formed by reaction of aniline yellow [4-(phenyldiazenyl)aniline] with 5-sulfosalicylic acid and benzenesulfonic acid, and a 1:2 nontransfer adduct compound with 3,5-dinitrobenzoic acid have bee …
The structures of two 1:1 proton-transfer red-black dye compounds formed by reaction of aniline yellow [4-(phenyldiazenyl)a
Viability assessment of spermatozoa in large falcons (Falco spp.) using various staining protocols.
Fischer D, Schneider H, Failing K, Meinecke-Tillmann S, Wehrend A, Lierz M. Fischer D, et al. Reprod Domest Anim. 2020 Oct;55(10):1383-1392. doi: 10.1111/rda.13785. Epub 2020 Aug 17. Reprod Domest Anim. 2020. PMID: 32722862
Eosin blue 2% [EB], eosin blue 2% with the addition of 3% sodium citrate [EB2], eosin blue-nigrosin 5% [EBN5], eosin yellow-nigrosin 5% [EYN5], eosin yellow-nigrosin 10% [EYN10], eosin blue-aniline blue [EBA], eosin yellow-aniline blue [EYA] and …
Eosin blue 2% [EB], eosin blue 2% with the addition of 3% sodium citrate [EB2], eosin blue-nigrosin 5% [EBN5], eosin yellow-nigrosin …
The cosmetic dye quinoline yellow causes DNA damage in vitro.
Chequer FM, Venâncio Vde P, de Souza Prado MR, Campos da Silva e Cunha Junior LR, Lizier TM, Zanoni MV, Rodríguez Burbano R, Bianchi ML, Antunes LM. Chequer FM, et al. Mutat Res Genet Toxicol Environ Mutagen. 2015 Jan 1;777:54-61. doi: 10.1016/j.mrgentox.2014.11.003. Epub 2014 Nov 18. Mutat Res Genet Toxicol Environ Mutagen. 2015. PMID: 25726175
Quinoline yellow (QY) is a chinophthalon derivative used in cosmetic compositions for application to the skin, lips, and/or body surface. ...
Quinoline yellow (QY) is a chinophthalon derivative used in cosmetic compositions for application to the skin, lips, and/or body surf …
Phytoremediation of aniline by Salix babylonica cuttings: Removal, accumulation, and photosynthetic response.
Li K, Li H, Li C, Xie H. Li K, et al. Ecotoxicol Environ Saf. 2021 May;214:112124. doi: 10.1016/j.ecoenv.2021.112124. Epub 2021 Mar 10. Ecotoxicol Environ Saf. 2021. PMID: 33711578 Free article.
The experiment showed that S. babylonica has a strong removal effect on aniline wastewater. Cuttings from S. babylonica stems and roots played an important role in accumulating aniline. ...Salix babylonica can endure moderate concentrations of aniline and has …
The experiment showed that S. babylonica has a strong removal effect on aniline wastewater. Cuttings from S. babylonica stems and roo …
Neuraminidase-triggered activation of prodrug-type substrate of 4-nitroaniline.
Matsushita T, Danyel MN, Koyama T, Hatano K, Matsuoka K. Matsushita T, et al. Bioorg Med Chem Lett. 2020 Jan 15;30(2):126883. doi: 10.1016/j.bmcl.2019.126883. Epub 2019 Dec 10. Bioorg Med Chem Lett. 2020. PMID: 31859155
Neuraminidase-mediated hydrolysis of the sialic acid moiety of the substrate initiates self-immolative elimination of the linker moiety, leading the liberation of yellow-colored reporter 4-nitroaniline. The elimination process involves generation of quinone methide interme …
Neuraminidase-mediated hydrolysis of the sialic acid moiety of the substrate initiates self-immolative elimination of the linker moiety, lea …
Plasmid-encoded genes specifying aniline oxidation from Acinetobacter sp. strain YAA.
Fujii T, Takeo M, Maeda Y. Fujii T, et al. Microbiology (Reading). 1997 Jan;143 ( Pt 1):93-99. doi: 10.1099/00221287-143-1-93. Microbiology (Reading). 1997. PMID: 9025282
Acinetobacter sp. strain YAA is able to use aniline and o-toluidine as the sole carbon and energy source. This strain has several different plasmids and acridine orange curing suggested that aniline utilization in strain YAA was plasmid-encoded. ...A recombinant E. …
Acinetobacter sp. strain YAA is able to use aniline and o-toluidine as the sole carbon and energy source. This strain has several dif …
Generation of aniline from a subsidiary colour of food yellow no. 5 (sunset yellow FCF).
Yamada M, Morimoto T, Nakamura M, Nakazawa H. Yamada M, et al. Food Addit Contam. 2000 May;17(5):379-86. doi: 10.1080/026520300404789. Food Addit Contam. 2000. PMID: 10945104
The formation of aniline from sodium salt of 6-hydroxy-5-(phenylazo)-2-naphthalenesulphonic acid (SS-AN, C.I. 15970, Orange RN), a subsidiary colour in the Japanese colour additive Food Yellow No. 5 (Y-5, C.I. 15985, Sunset Yellow FCF), was investigated in th …
The formation of aniline from sodium salt of 6-hydroxy-5-(phenylazo)-2-naphthalenesulphonic acid (SS-AN, C.I. 15970, Orange RN), a su …
521 results