<<< Back to Sampling and Analytical Methods Link to Printing Instructions Printing Instructions

For problems with accessibility in using figures, illustrations and PDFs in this method, please contact
the SLTC at (801) 233-4900. These procedures were designed and tested for internal use by OSHA personnel.
Mention of any company name or commercial product does not constitute endorsement by OSHA.


Related Information: Chemical Sampling - Amitrole
Method number: PV2006

Target Concentration:0.2 mg/m3 (ACGIH TLV-TWA)
Procedure: Samples are collected by drawing known volumes of air through impingers containing water. Samples are analyzed by high performance liquid chromatography (HPLC) using a UV detector.
Recommended air volume and sampling rate: 60 L at 1 Lpm
Detection limit of the overall procedure (based on the recommended air volume): 0.004 mg/m3
Status of method:Stopgap method. This method has been only partially evaluated and is presented for information and trial use.
December 1987 Yihlin Chan
Carcinogen and Pesticide Branch
OSHA Analytical Laboratory
Salt Lake City, Utah

1. General discussion
1.1. Background

The OSHA Analytical Laboratory received a set of samples requesting analysis of amitrole. The samples had been collected in impingers containing water. This report describes the preliminary validation of the sampling method and the analytical method developed for amitrole.

1.2. Toxic effects (This section is for information only and should not be taken as the basis of OSHA policy.)

"The oral LD50 of amitrole in mice was 11,000 or 14,700 and was 25,000 mg/kg in rats. The intravenous LD50 was 5000 mg/kg in mice. The dermal application of 10,000 mg/kg was tolerated by rats and rabbits without any systemic effects. The exposure of rats for four hours to an aerosol of 439 mg/m3 did not produce symptoms of poisoning and did not irritate the eyes and the upper respiratory tract. It has a very slight irritating effect on the skin and eyes of rabbits." (Ref. 5.5)

The ACGIH TLV Committee recommended the removal of the A2 designation as a suspected human carcinogen from the listing for amitrole in 1984. (Ref. 5.5)

1.3. Potential workplace exposure (Ref. 5.4)

Amitrole is used as an herbicide and a plant growth regulator. No estimate on the extent of workplace exposure could be found.

1.4. Physical properties (Ref. 5.1 and 5.2)

Chemical name: 3-Amino-1,2,4-triazole
Synonyms: 3-Amino-1H-1,2,4-triazole; aminotriazole; ATA; ENT 25445; Amizol; Cytrol; Weedazol
CAS no. 61-82-5
Molecular formula: C2H4N4
Molecular weight: 84.1
Appearance: Colorless crystals; bitter taste
Melting point: 159°C
Solubility: Soluble in water (28% at 25°C) and ethanol (26% at 75°C); slightly soluble in chloroform, methylene chloride, acetonitrile, and ethyl acetate; insoluble in ether, acetone and hydrocarbons
UV scan: See Figure 3.
Structure: Structure

1.5. Detection limit of the analytical procedure

The detection limit of the analytical procedure is 0.51 ng per injection. This is the amount of analyte which will give a peak whose height is approximately 5 times the baseline noise.
2. Sampling procedure
2.1. Apparatus and reagents
2.1.1. A personal sampling pump that can be calibrated to within 5% of the recommended flow rate

2.1.2. Impinger

2.1.3. Distilled water
2.2. Sampling procedure (Ref. 5.3)
2.2.1. Calibrate pump.

2.2.2. Attach the collection device to the shirt collar or within the breathing zone. Position the tubing so as not to interfere with the work of the employee.

2.2.3. Turn on pump and record the starting time.

2.2.4. Check the pump flow periodically.

2.2.5. Prepare a blank.

2.2.6. At the end of the sampling period, turn off the pump and record the ending time.

2.2.7. Transfer the impinger solution to a vial. Rinse with a small amount water and pour the rinse solution into the vial. Seal the vial with an OSHA-21.
2.3. Recommended air volume and sampling rate
2.3.1. The recommended air volume is 60 L. 2.3.2. The recommended sampling rate is 1 Lpm.
2.4. Extraction efficiency

Not performed. Samples are analyzed directly.

2.5. Retention efficiency

Three impingers containing 15 mL of water were each spiked with 12.71 ug of amitrole. Humid air (80% RH, 60 L @ 1 Lpm) was drawn through the solutions. The solutions were each made 15.0 mL with water and analyzed. The average recovery was 87.5%.

Sample recovered Recovery
---------- --------------- ----------
YCA1 11.30 ug 88.9%
YCA2 10.91 ug 85.8%
YCA3 11.17 ug 87.9%
---------- --------------- ----------
Average = 87.5%

2.6. Storage

Three impingers containing 15 mL of water were each spiked with 12.71 ug of amitrole. Humid air (80% RH, 60 L @ 1 Lpm) was drawn through the solutions. The solutions were transferred to scintillation vials and stored at room temperature in the dark for 33 days. The average recovery was 79.9%.

Sample recovered Recovery
---------- --------------- ----------
YCA4 9.34 ug 73.5%
YCA5 10.48 ug 82.5%
YCA6 10.62 ug 83.6%
---------- --------------- ----------
Average = 79.9%

2.7. Interferences

There are no known interferences to the sampling procedure.
3. Analytical method
3.1. Apparatus
3.1.1. High performance liquid chromatograph

3.1.2. Chromasil Cl8 column or equivalent

3.1.3. UV detector

3.1.4. Stripchart recorder
3.2. Reagents
3.2.1. Water, HPLC grade

3.2.2. Amitrole, EPA #0200
3.3. Standard preparation

Weigh 5 to 10 mg of amitrole in a 10-mL volumetric flask. Add water to the mark. Dilute with water to a suitable working range.

3.4. Sample preparation

The volumes of the samples were made 15.0 mL with distilled water.

3.5. Analysis
3.5.1. Instrument conditions

Column: Chromasil C18
Eluent: 100% water
Flow rate: 1.0 mL/min
Detector: 205 nm
Injection size: 30 uL
Retention time: 6.0 min

3.5.2. Chromatogram (See Figure 1)
3.6. Interferences
3.6.1. Any collected compound that has the same retention time as amitrole and absorbs at 205 nm is a potential interference. Generally, chromatographic conditions can be altered to separate an interference from the analyte.

3.6.2. Retention time alone is not proof of a chemical identity. Confirmation by other means should be sought whenever possible.
3.7. Calculations
3.7.1. A calibration curve is constructed by plotting standard concentrations versus detector response (see Figure 2).

3.7.2. The concentration of a sample is determined from the calibration curve.

3.7.3. The air concentration is determined by the formula:

mg/m3 = (µg/mL)(15 mL)
(air volume, L)

4. Recommendations for further study
4.1. Investigate a more convenient sampling device, such as a sorbent tube or a filter.

4.2. Develope a fully validated method.

For problems with accessibility in using figures please contact the SLTC at (801) 233-4900.

Figure 1. Chromatogram of Amitrole

For problems with accessibility in using figures please contact the SLTC at (801) 233-4900.

Figure 2. Calibration Curve of Amitrole

For problems with accessibility in using figures please contact the SLTC at (801) 233-4900.

Figure 3. UV Scan of Amitrole in Water
5. References
5.1. "Registry of Toxic Effects of Chemical Substances, 1983-84 Supplement"; U.S. Department of Health and Human Services: Cincinnati, OH, 1986; DHHS(NIOSH) Publication No. 86-103.

5.2. Windholz, M., Ed. "Merck Index", 9th ed.; Merck and Co: Rahway, NJ, 1979.

5.3. "Industrial Hygiene Technical Manual", OSHA Instruction CPL 2-2.20A, March 30, 1984, U.S. Department of Labor. Chapter II: "Standard Methods for Sampling Air Contaminants."

5.4. WHO, "IARC Monograph on the Evaluation of the Carcinogenic Risk of Chemicals to Man", Volume 13; International Agency for Research on Cancer: Lyon, 1977, pp. 201-218.

5.5. "Documentation of the Threshold Limit Values and Biological Exposure Incices", Fifth Edition, American Conference of Governmental Industrial Hygienists Inc., Cincinnati, OH, 1986.

Page current as of: 09/29/2008