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100900 Aldrich

4-Bromoaniline

97%

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Properties

Related Categories Amines, Building Blocks, C6, Chemical Synthesis, Nitrogen Compounds,
assay   97%
mp   56-62 °C(lit.)

Description

Packaging

5, 100, 500 g in glass bottle

Price and Availability

Suggested Laboratory Gloves


Laboratory GlovesThis substance has been tested against several types of hand protection for CE compliance. Click below to find the recommended gloves for handling this product.



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Safety & Documentation

Safety Information

Symbol 
GHS06  GHS06
Signal word 
Danger
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
Hazard Codes (Europe) 
Xn
Risk Statements (Europe) 
Safety Statements (Europe) 
26-36/37
RIDADR 
UN 2811 6.1 / PGIII
WGK Germany 
3
RTECS 
BW9280000

Protocols & Articles

Peer-Reviewed Papers

References

Set your institution to view full text papers.

A re-evaluation of the D (+) xylose absorption test in the horse. Roberts MC and Norman P Equine Vet. J. 11(4), 239-43, (1979)

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The effect of varying halogen substituent patterns on the cytochrome P450 catalysed dehalogenation of 4-halogenated anilines to 4-aminophenol metabolites. Cnubben NH, Vervoort J, Boersma MG, et al. Biochem. Pharmacol. 49(9), 1235-48, (1995)

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Sensitization of multidrug resistant (MDR) cancer cells to vinblastine by novel acridones: correlation between anti-calmodulin activity and anti-MDR activity. Mayur YC, Padma T, Parimala BH, et al. Med. Chem. 2(1), 63-77, (2006)

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Identification of the urinary metabolites of 4-bromoaniline and 4-bromo-[carbonyl-13C]-acetanilide in rat. Scarfe GB, Nicholson JK, Lindon JC, et al. Xenobiotica 32(4), 325-37, (2002)

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Cosorption study of organic pollutants and dissolved organic matter in a soil. Flores-Céspedes F, Fernández-Pérez M, Villafranca-Sánchez M, et al. Environ. Pollut. 142(3), 449-56, (2006)

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High-performance liquid chromatography and inductively coupled plasma mass spectrometry (HPLC-ICP-MS) for the analysis of xenobiotic metabolites in rat urine: application to the metabolites of 4-bromoaniline. Nicholson JK, Lindon JC, Scarfe G, et al. Analyst 125(2), 235-6, (2000)

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Theoretical Raman and infrared spectra, and vibrational assignment for para-halogenoanilines: DFT study. Wojciechowski PM and Michalska D Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 68(3), 948-55, (2007)

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Electrophilic properties of patulin. Adduct structures and reaction pathways with 4-bromothiophenol and other model nucleophiles. Fliege R and Metzler M Chem. Res. Toxicol. 13(5), 363-72, (2000)

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Effects of dissolved organic carbon on sorption of 3,4-dichloroaniline and 4-bromoaniline in a calcareous soil. González-Pradas E, Fernández-Pérez M, Flores-Céspedes F, et al. Chemosphere 59(5), 721-8, (2005)

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Spectrophotometric determination of carnosine, anserine, and taurine in skeletal muscle. Parker CJ Anal. Biochem. 108(2), 303-5, (1980)

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Characterisation of putative pentose-containing conjugates as minor metabolites of 4-bromoaniline present in the urine of rats following intraperitoneal administration. Major H, Castro-Perez J, Nicholson JK, et al. Rapid Commun. Mass Spectrom. 17(1), 76-80, (2003)

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Potential of neurotoxicity after a single oral dose of 4-bromo-, 4-chloro-, 4-fluoro- or 4-iodoaniline in rats. Okazaki Y, Yamashita K, Ishii H, et al. J. Appl. Toxicol. 23(5), 315-22, (2003)

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Biopartitioning micellar chromatography to predict mutagenicity of aromatic amines. S Torres-Cartas et al Eur. J. Med. Chem. 42, 1396-402, (2007)

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Acute metobromuron poisoning with severe associated methemoglobinemia. Identification of four metabolites in plasma and urine by LC-DAD, LC-ESI-MS, and LC-ESI-MS-MS. Turcant A, Cailleux A, Le Bouil A, et al. J. Anal. Toxicol. 24(3), 157-64, (2000)

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Detection of mono- and di-hexoses as metabolites of 4-bromoaniline using HPLC-TOF-MS/MS. Major H, Castro-Perez J, Nicholson JK, et al. Xenobiotica 33(8), 855-69, (2003)

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Proton-transfer compounds of 8-hydroxy-7-iodoquinoline-5-sulfonic acid (ferron) with 4-chloroaniline and 4-bromoaniline. Smith G, Wermuth UD, and Healy PC Acta Crystallogr. C 63(Pt 7), o405-7, (2007)

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Merck 14,1404

Beil. 12,IV,1497

Aldrich MSDS 1, 229:A / Corp MSDS 1 (1), 498:B / FT-IR 2 (2), 2049:D / FT-IR 1 (1), 1207:C / FT-NMR 1 (2), 482:A / IR-Spectra (3), 724:A / IR-Spectra (2), 638:C / NMR-Reference 2 (1), 1010:C / RegBook 1 (1), 1397:D / Sigma FT-IR 1 (2), 331:D / Structure Index 1, 217:C:1 / Vapor Phase 3, 1127:A

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