Science Inventory

Mass Spectrometric Identification of An Azobenzene Derivative Produced by Smectite-Catalyzed Conversion of 3-Amino-4-Hydroxphenylarsonic Acid

Citation:

Wershaw, R. L., D. W. Rutherford, C. E. Rostad, J. R. Garbarino, I. FerrerFelis, K. R. Kennedy, G M. Momplaisir, AND A H. Grange. Mass Spectrometric Identification of An Azobenzene Derivative Produced by Smectite-Catalyzed Conversion of 3-Amino-4-Hydroxphenylarsonic Acid. TALANTA 59(6):1219-1226, (2003).

Impact/Purpose:

The overall goals of the task are to apply NERL's core capability in advanced chemical science and technology for maximum benefit in estimating exposures of ecosystems and humans to chemical stressors and to identify emerging pollution concerns, in particular long-range airborne transport of contaminants. This task comprises several subtasks, each with individual objectives:

Subtask 1: screen exposures of National Park PRIMENet ecosystems to chemical stressors, identifying indications of exposure requiring further evaluation, and use these samples evaluate new analytical methods as replacements for standard methods in future assessments of ecosystem contaminant exposures.

Subtask 2: evaluate a new mercury analytical approach with superior performance on complex solid matrices such as biological tissues, and apply the approach to estimating exposure of ecosystems and humans to mercury.

Subtask 3: determine distribution patterns of chemical contaminants in the southern Sierra Nevada Range of California, investigate topographic and weather factors that may influence the distributions, and determine if a correlation exists between contaminant distributions and extirpation patterns of the mountain yellow-legged frog.

Subtask 4: provide analytical methods to measure a number of inorganic and organic arsenic species in a variety of environmental matrices, elucidate the environmental transformations undergone by organoarsenic animal-feed additives, and determine if the potential exists for substantially increased exposure of humans and aquatic organisms to arsenic.

Description:

We report here the first evidence of a possible mechanism for the formation of an azobenzene arsonic acid compound in the environment The compound was formed when 3-amino-4-hydroxyphenylarsonic acid (3-amino-HPAA) was added to aqueous suspensions of smectite clay The 3-amino-HPAA is a degradation product excreted by chickens that are fed rations amended with roxarsone. Roxarsone is used to control coccidial intestinal parasites in most of the broiler chickens grown in the United States. The structure of the azobenzene arsonic acid compound was first inferred from negative- ion and positive-ion low-resolution mass-spectrometric analyses of the supernatant of the smectite suspension. Elemental composition of the parent ion determined by high-resolution positive-ion mass spectrometric measurements was consistent with the proposed structure of the azobenzene arsonic acid compound.

Record Details:

Record Type:DOCUMENT( JOURNAL/ PEER REVIEWED JOURNAL)
Product Published Date:03/25/2003
Record Last Revised:09/02/2020
Record ID: 65235