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Azinphos-Methyl

Related Information: Chemical Sampling - Azinphos-Methyl
Method no.: PV2087

Control no.: T-PV2087-01-8906-CH

Matrix: Air

Target Concentration: 0.2 mg/m3 Skin (OSHA PEL and ACGIH TLV)

Procedure: Samples are collected by drawing known volumes of air through OSHA versatile sampler (OVS-2) tubes, each containing a glass fiber filter and two sections of XAD-2 adsorbent. Samples are extracted with toluene and analyzed by gas chromatography (GC) using a flame photometric detector (FPD). 

Recommended air volume and sampling rate: 480 L at 1.0 L/min

Detection limit of the overall procedure (based on the recommended air volume and the analytical detection limit): 0.0089 mg/m3

Status of method: Stopgap method. This method has been partially evaluated and is presented for information and trial use only.

June 1989  David B. Armitage 

Carcinogen and Pesticide Branch 
OSHA Analytical Laboratory 
Salt Lake City, Utah 


1. General Discussion
1.1 Background
1.1.1 History of procedure

This evaluation was undertaken to determine the effectiveness of the OVS-2 tube as a sampling device for azinphos-methyl. It follows the procedure developed for several other organophosphorus pesticides. (Ref. 5.1

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

The following paragraph is excerpted from the book OCCUPATIONAL DISEASES, A Guide To Their Recognition. (Ref. 5.2
The organic phosphorus compounds act as irreversible inhibitors of cholinesterase, thereby allowing the accumulation of large amounts of acetylcholine. When a critical level of cholinesterase depletion is reached, usually about 20% of normal, symptoms and signs of acetylcholine accumulation poisoning become manifest. Symptoms may include blurred vision, weakness, nausea, headache, abdominal cramps, chest discomfort, and diarrhea. Signs may include miosis, muscle twitching, salivation, sweating, tearing, cyanosis, convulsions, and coma. 
Besides being absorbed following inhalation or ingestion, organophosphorus pesticides are readily absorbed through the intact skin (Ref. 5.2). When a particular pesticide has a low dermal LD50, a skin notation should be added to the TLV or PEL. 

Azinphos-methyl has an acute oral LD50 of 11 to 13 mg/kg for rats and an acute dermal LD50 of 220 mg/kg for rats. (Ref. 5.3

Due to these factors the ACGIH has established a TLV-TWA of 0.2 mg/m3, with a skin notation, for azinphos-methyl. (Ref. 5.3

OSHA has established this same value as its PEL. 

1.1.3 Potential workplace exposure 

No estimate of worker exposure to azinphos-methyl could be found. Azinphos-methyl is used as an insecticide. (Ref. 5.3

1.1.4
Physical properties (Ref. 5.3-5.5
Molecular weight: 317.34
Molecular formula: C10H12N303PS2
CAS #: 86-50-0
IMIS #: 0300
Melting point: 73-74C, unstable at more than 200C
Vapor Pressure: no information found
Appearance: brown, waxy solid
Solubility: 20 ppm in water at 25C soluble in most organic solvents, except aliphatics
Synonyms: Bay 17147, Carfene, Cotnion-Methyl, Gusathion M, Guthion, metiltriazotion 
Chemical name: O,O-Dimethyl S-[4-oxo-1,2,3-benzo-
triazin-3(4H)-yl-methyl]phosphoro-dithioate


Structure: 
Structure
1.2 Limit defining parameters 

The detection limit of the analytical procedure is 0.16 ng per injection. This is the amount of analyte which will give a peak whose height is approximately five times the baseline noise. This detection limit takes into account a split ratio of 13.4 to 1 used on the capillary GC. 
2. Sampling Procedure 
2.1 Apparatus 
2.1.1 A personal sampling pump that can be calibrated to within 5% of the recommended flow rate with the sampling device in line. 

2.1.2 OVS-2 tubes, which are specially made 13-mm o.d. glass tubes that are tapered to 6-mm o.d. They are packed with a 140-mg backup section and a 270-mg sampling section of cleaned XAD-2. The backup section is retained by two foam plugs and the sampling section is between one foam plug and a 13-mm diameter glass fiber filter. The glass fiber filter is held next to the sampling section by a polytetrafluoroethylene (PTFE) retainer. (See Figure 1.) 
2.2 Reagents 

No sampling reagents are required.

2.3 Sampling technique 
2.3.1 Attach the small end of the OVS-2 sampling tube to the sampling pump with flexible, plastic tubing such that the large, front section of the sampling tube is exposed directly to the atmosphere. Do not place any tubing in front of the sampler. 

2.3.2 Attach the sampler vertically (large end down) in the worker's breathing zone in such a manner that it does not impede work performance. 

2.3.3 After sampling for the appropriate time, remove the sampling device and seal the tube with plastic end caps. 

2.3.4 Wrap each sample end-to-end with an OSHA seal (Form 21).

2.3.5 Submit at least one blank with each set of samples. Handle the blank the same as the other samples, but do not draw air through it. 

2.3.6 Submit any bulk samples in a separate container. Do not ship them with the air samples. 
2.4 Desorption efficiency 

A glass fiber filter and an amount of XAD-2 adsorbent equal to the sampling section (270 mg) of an OVS-2 tube were placed in each of six 4-mL vials. These vials were then sealed with PTFE-lined septa. 

Five of the vials were then each liquid spiked with 22 L of a 4.22 mg/mL solution of azinphos-methyl in toluene by injecting through the septum onto the glass fiber filter. After replacing the punctured septums, these vials were allowed to equilibrate overnight in a drawer at room temperature. They were then desorbed with 2.0 mL of toluene containing triphenyl phosphate (TPP) as an internal standard and analyzed as in Section 3.5
Table 2.4
Desorption Study 

Vial # Amount spiked Amount recovered % Recovery

EX 1 92.84 g 93.58 g 100.8
EX 2 92.84 g 90.70 g 97.7
EX 3 92.84 g 96.28 g 103.7
EX 4 92.84 g 90.61 g 97.6
EX 5 92.84 g 85.13 g 91.7
EX 6 0.00 g 0.00 g Blank

 Average recovery is 98.3% 
2.5 Retention efficiency 

Six OVS-2 tubes were each liquid spiked with 22 L of a 4.22 mg/mL solution of azinphos-methyl in toluene by spiking the glass fiber filter. These tubes were then sealed with plastic end caps and placed in drawer at room temperature. After overnight storage, 480 liters of humid air (approximately 70% relative humidity) were drawn through each tube. Three of these tubes, along with a blank tube, were then desorbed and analyzed as in Section 3. No azinphos-methyl was found on the backup sections of these tubes. 
Table 2.5
Retention Efficiency Study 

Tube # Amount spiked Amount recovered % Recovery

RET 1 92.84 g 82.44 g 88.8
RET 2 92.84 g 85.97 g 92.6
RET 3 92.84 g 84.76 g  91.3
RET 4 0.00 g 0.00 g Blank

Average recovery is 90.9% 
2.6 Sample storage 

The remaining three spiked tubes from Section 2.5. (and a blank tube) were stored for a total of 8 days in a drawer at room temperature. They were then desorbed and analyzed as in Section 3. No azinphos-methyl was found in the backup sections of these tubes. 
Table 2.6 
Storage Study 

Tube  Amount spiked Amount recovered % Recovery

ST 1  92.84 g 85.51 g 92.1
ST 2 92.84 g 86.43  g 93.1
ST 3 92.84 g 93.03  g 100.2
ST 4 0.00 g 0.00  g Blank

Average recovery is 95.1% 
2.7 Recommended air volume and sampling rate 
2.7.1 The recommended air volume is 480 L. 

2.7.2 The recommended flow rate is 1.0 L/min. 
2.8 Interferences (sampling) 

It is not known if any compounds will interfere with the collection of azinphos-methyl. Suspected interferences should be reported to the laboratory with submitted samples. 

2.9 Safety precautions (sampling) 
2.9.1 Attach the sampling equipment in such a manner that it will not interfere with work performance or employee safety. 

2.9.2 Follow all safety practices that apply to the work area being sampled. 
3. Analytical Procedure
3.1 Apparatus 
3.1.1 A GC equipped with an FPD. A Hewlett-Packard 5890A GC (capillary) equipped with both an FPD operating in the phosphorus mode and a Hewlett-Packard 7673A automatic sampler was used in this evaluation. 

3.1.2 A GC column capable of separating azinphos-methyl from any interferences. A 45 m 0.2 mm i.d. SE-54 capillary column, 0.25 m thick film, was used in this evaluation and is available from Supelco, Inc., Bellefonte, PA. 

3.1.3 An electronic integrator or other suitable means of measuring detector response. A Hewlett-Packard 3392A Integrator and a Hewlett-Packard 3357 data system were used in this evaluation. 

3.1.4 Vials, 4-mL and 2-mL glass with PTFE-lined septa.

3.1.5 Volumetric flasks, pipets, and syringes.
3.2 Reagents 
3.2.1 Hydrogen, air, and nitrogen, GC grade. 

3.2.2 Toluene, Pesticide grade. 

3.2.3 Azinphos-methyl. A 98.7% pure standard from EPA was used in this evaluation. 

3.2.4 Triphenyl phosphate (TPP), practical grade from J.T. Baker. If an internal standard method is used, the desorbing solution is prepared by adding the internal standard to the toluene. A 40 g/mL solution of TPP was used as the internal standard in this evaluation. 
3.3 Standard preparation 
Prepare stock standards by adding either toluene or desorbing solution (if an internal standard is used) to preweighed amounts of azinphos-methyl. Prepare working range standards by diluting stock solutions with either toluene or desorbing solution (if an internal standard is used). Store stock and dilute standards in a freezer. 
3.4 Sample preparation 
3.4.1 Transfer the 13-mm glass fiber filter and the 270-mg sampling section of the tube to a 4-mL vial. Place the first foam plug and the 140-mg backup section in a separate vial. A small glass funnel can be used to facilitate the transfer of the adsorbent. Discard the rear foam plug. Do not discard the glass sampling tube, it can be reused. 

3.4.2 Add 2.0 mL of either toluene or desorbing solution (if an internal standard is used) to each vial. 

3.4.3 Seal the vials with PTFE-lined septa and allow them to desorb for one hour. Shake the vials by hand periodically during this time. 

3.4.4 If necessary, transfer aliquots of the samples to the vials used in GC analysis. In this evaluation the samples were transferred to 2-mL glass vials, sealed with PTFE-lined septa and loaded on the automatic sampler. 
3.5 Analysis 
3.5.1 Analytical conditions (These conditions were developed for a series of organophosphorus pesticides, which was run in several groups. See Figure 2. for the group containing azinphos-methyl.) 
GC conditions
GC column: 45 m 0.2 mm i.d. SE-54, 0.25 m thick film 
Carrier gas: hydrogen 
Flow rate: 2.05 mL/min at 220C
Split ratio: 13.4 to 1 at 220C
Retention time: 17.26 min
Injector conditions 
Temperature: 250C
Volume: 1 L 
Oven temperature program 
Initial temperature: 220C
Initial time: 5 min
Rate: 15C/min
Final temperature: 260C
Final time: 15 min
FPD conditions 
Hydrogen flow rate: 75 mL/min
Air flow rate: 100 mL/min
Auxiliary gas: nitrogen
Flow rate: 28 mL/min
Temperature: 250C
3.5.2 Chromatogram (See Figure 2.) 
3.6 Interferences (analytical) 
3.6.1 Any compound having a retention time similar to that of the analyte is a potential interference. Generally, chromatographic conditions can be altered to separate 
interferences from the analyte. 

3.6.2 Retention time on a single column is not proof of chemical identity. Analysis by an alternate GC column, detection by an FPD in the sulfur mode and confirmation by mass spectrometry are additional means of identification. 
3.7 Calculations 
3.7.1 Construct a calibration curve by plotting detector response versus standard concentration. 

3.7.2 Determine the concentration of azinphos-methyl in each sample from the calibration curve. If azinphos-methyl is found on the backup section, make blank corrections for each section separately before adding the results together. 

3.7.3 Determine the air concentration by the following formula. 

  (μg/mL)(desorption volume, mL)
mg/m2 =
    (air volume, L)(desportion efficiency, decimal)
3.8 Safety precautions (analytical) 
3.8.1 Avoid exposure to all standards. 

3.8.2 Avoid exposure to all solvents. 

3.8.3 Wear safety glasses at all times. 
4. Recommendations for Further Study
This method should be fully validated.
  For problems with accessibility in using figures please contact the SLTC at (801) 233-4900.
Figure 1. OVS-2 Sampling Device
 
For problems with accessibility in using figures please contact the SLTC at (801) 233-4900.

Figure 2. Chromatogram of Azinphos-methyl 
This chromatogram also contains TPP and other pesticides. 
5. References 
5.1 Burright, D.; Method #62, "Chlorpyrifos, DDVP, Diazinon, Malathion, and Parathion"; OSHA Analytical Laboratory, unpublished, 1986. 

5.2 "OCCUPATIONAL DISEASES, A Guide to their Recognition"; U.S. Department of Health, Education, and Welfare; Public Health Service, Public Health Service Publication No. 1097, U.S. Government Printing Office: Washington, D.C., 1964; p 245. 

5.3 "Documentation of the Threshold Limit Values and Biological Exposure Indices", 5th ed.; American Conference of Governmental Industrial Hygienists: Cincinnati, OH, 1986; p 46. 

5.4 "Farm Chemicals Handbook"; Meister Publishing Co.: Willoughby, OH, 1986; p C24. 

5.5 Windholz, M., Ed.; "Merck Index", 10th ed.; Merck and Co.: Rahway, NJ, 1983; p 131.