<<< 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.

Catechol (Pyrocatechol)

Related Information: Chemical Sampling - Catechol
Method number: PV2014
 
Matrix:Air
 
Target concentration: 5 ppm (20 mg/m3) OSHA TWA PEL
 
Procedure: Samples are collected by drawing a known volume of air through an OVS-7 tube. Samples are desorbed with methanol and analyzed by gas chromatography with a flame ionization detector (GC-FID).
 
Air volume and sampling rate studied: 100 liters at 1.0 Lpm.
 
Status of method: Stopgap method. This method has been only partially evaluated and is presented for information and trial use.
 
Date: August, 1992 Chemist: Mary E. Eide



Organic Service Branch I
OSHA Salt Lake Technical Center
Salt Lake City, Utah



1. General Discussion
1.1. Background
1.1.1. History of procedure

The OSHA Technical Center has received many requests for a sampling and analytical procedure for catechol. OSHA promulgated an exposure standard for catechol of 5 ppm (20 mg/m3) TWA. OSHA method 32 recommends collection of phenol and cresol on XAD-7 tubes and desorption with methanol (Ref. 5.1). Catechol is related to these compounds, and is a solid at room temperature, so a modification of method 32 was tried using an OVS-7 tube instead of the XAD-7. An OVS-7 tube contains a glass fiber filter, which would trap any particulates, followed by a 270 mg section of XAD-7 resin then a 140 mg section. Desorption, retention and storage recoveries were good using OVS-7 tubes.

1.1.2. Potential workplace exposure (Ref. 5.2 and 5.3)

Catechol is used as a topical antiseptic, reagent, antifungal preservative on seed potato pieces, photographic developer, and developer in fur dyes. Catechol is used as an antioxidant in many industries including rubber, chemical, dye, photographic, pharmaceutical, fat, cosmetics, and oil.

1.1.3. Toxic Effects (This section is for information purposes and should not be taken as the basis for OSHA policy.)(Ref. 5.3)

The lethal human dose of catechol is 50 to 500 grams/kilogram, or 1 teaspoon to 1 ounce for a 70 kilogram (150 pound) person, with death resulting from pulmonary failure. Catechol is a skin, eye, mucous membrane, and pulmonary irritant. It is readily absorbed from the gastrointestinal tract, and through the skin. Catechol can cause elevated blood pressure through vasoconstriction, degeneration of the renal tubes in the kidneys, and diminished liver function.

1.1.4. Physical properties (Ref. 5.2):

Compound: Structure
Synonyms: 1,2-Benzenediol; o-Benzenediol; Catechin; o-Dioxybenzene; 1,2-dihydroxybenzene; Fouramine 68; o-Hydroxyphenol; o-Hydroquinone; 2-Hydroxyphenol; CI Oxidation Base 26; Fouramine PCH; o-Diphenol; Durafur Developer C; Oxyphenic acid; o-Phenylenediol; Phthalhydroquinone; Pyrocatechin; pyrocatechol; Pyrocatechuic acid
Molecular weight: 110.11
Melting point: 105°C
Boiling point: 245.5°C
Flash point: 127°C (261°F)
Odor: faintly musty phenolic
Color: colorless to white crystals
Molecular formula: C6H6O2
CAS: 120-80-9
IMIS: 0571
RTECS: 73250; UX1050000
1.2. Limit defining parameters
1.2.1. The detection limit of the analytical procedure is 2.1 µg/mL catechol in the desorbing solvent. This is the smallest amount that could be detected under normal operating conditions.

1.2.2. The overall detection limit is 0.014 ppm catechol. (All ppm amounts in this study are based on a 100 liter air volume and 3 mL desorption.)
1.3. Advantages
1.3.1. The sampling procedure is convenient.

1.3.2. The analytical method is reproducible and sensitive.

1.3.3. Reanalysis of samples is possible.

1.3.4. It may be possible to analyze other compounds at the same time.

1.3.5. Interferences may be avoided by proper selection of column and GC parameters.
1.4. Disadvantages

none known
2. Sampling procedure
2.1. Apparatus
2.1.1. A calibrated personal sampling pump, the flow of which can be determined within ± 5% at the recommended flow.

2.1.2. The sampling media consists of OVS-7 tubes. The OVS-7 tubes are specially made 13 mm O.D.. glass tubes that are tapered to 6 mm O.D.. These tubes are packed with a 13 mm diameter glass fiber filter then a 270 mg sampling section followed by a 140 mg backup section of purified XAD-7 resin, available from Alltech. There is a foam plug between sampling section and backup section and after the backup section. The glass fiber filter is held next to the sampling section by a polytetrafluoroethylene (PTFE) retainer.(Figure 1) These tubes are commercially available through many sources.
2.2. Sampling technique
2.2.1. Remove the end caps of the OVS-7 immediately before sampling.

2.2.2. Connect the OVS-7 to the sampling pump with flexible tubing.

2.2.3. Place the tubes in a vertical position to minimize section towards the channeling, with the smaller pump.

2.2.4. Air being sampled should not pass through any hose or tubing before entering the OVS-7.

2.2.5. Seal the OVS-7 with plastic caps immediately after sampling. Seal each sample lengthwise with OSHA Form-21 sealing tape.

2.2.6. With each batch of samples, submit at least one blank tube from the same lot used for samples. This tube should be subjected to exactly the same handling as the samples (break ends, seal, & transport) except that no air is drawn through it.

2.2.7. Transport the samples (and corresponding paperwork) to the lab for analysis.

2.2.8. Bulks submitted for analysis must be shipped in a separate mailing container from other samples.
2.3. Desorption efficiency
2.3.1. Two hundred seventy milligram portions of XAD-7 resin were placed into separate 4 mL vials and six portions were spiked at each loading of 0.205 mg (0.455 ppm), 1.02 mg (2.26 ppm), 2.05 mg (4.55 ppm), and 4.01 mg (8.9 ppm) catechol, and allowed to equilibrate overnight at room temperature. They were desorbed with 3 mL of the desorbing solution for 30 minutes with occasional shaking, and analyzed by GC-FID. The overall average was 98.1%.(Table 1)
Table 1
Desorption Efficiency

Portion % Recovered
# 0.205 mg 1.02 mg 2.05 mg 4.01 mg

1 99.1 99.1 99.8 95.0
2 96.6 99.7 99.0 97.0
3 97.2 98.1 100 99.5
4 98.6 98.7 97.4 97.1
5 98.4 99.1 96.5 98.6
6 97.5 97.3 98.5 96.4
average 97.9 98.7 98.5 97.3
overall average 98.1
standard deviation ± 1.28



2.3.2. Six filters were placed into separate 4 mL vials and spiked at each loading of 0.193 mg (0.429 ppm), 0.96 mg (2.13 ppm), 1.93 mg (4.29 ppm), and 4.00 mg (8.88 ppm) catechol and allowed to equilibrate overnight at room temperature. They were extracted with 3 mL of the desorbing solution for 30 minutes with occasional shaking, and were analyzed by GC-FID. The overall average was l00%.(Table 2)
Table 2
Desorption Efficiency

Filter % Recovered
# 0.193 mg 0.96 mg 1.93 mg 4.00 mg

1 100 102 98.7 98.6
2 100 99.3 100 98.9
3 99.8 99.9 101 99.9
4 102 99.8 101 99.9
5 101 99.9 101 99.4
6 98.0 100 99.7 99.9
average 100 100 100 99.6
overall average 100
standard deviation ± 0.998



2.4. Retention efficiency

The filters of six OVS-7 tubes were spiked with 2.0 mg (4.44 ppm) catechol, allowed to equilibrate overnight and then had 100 liters humid air (91% RH) pulled through them. The glass fiber filter was placed before the Teflon spacer to insure that no catechol spiked onto the filter was in contact with the XAD-7 sections before the humid air was drawn. They were opened, desorbed and analyzed by GC-FID. The retention efficiency averaged 98.6%. There was no catechol found on the backup portions of the tubes. The amount found on the front adsorbent portion of the OVS-7 tubes indicates that catechol is too volatile to be collected on glass fiber filters.(Table 3)
Table 3
Retention Efficiency

Tube # % Recovered % Recovered % Recovered Total
Filter 'A' 'B'

1 85.9 14.0 0.0 99.9
2 83.7 14.2 0.0 97.9
3 75.5 20.8 0.0 96.3
4 84.1 15.9 0.0 100
5 78.0 20.6 0.0 98.6
6 83.8 15.3 0.0 99.1
average 98.6



2.5. Storage

Glass fiber filters(GFF) from the OVS-7 tubes were removed and spiked with 2.23 mg (4.95 ppm) catechol and placed in a 4 mL vial containing the front section of XAD-7 resin, and stored at room temperature until opened and analyzed. Catechol may degrade when exposed to light, so half of the vials were stored in room light and the other half were stored in a drawer. The recoveries averaged 98.6% for the 14 days stored, with little difference between the samples stored under room light and those stored in a drawer, indicating catechol is stable on OVS-7 tubes in the light. The catechol vaporized off the glass fiber filters and was adsorbed by the XAD-7 resin, with more of the catechol migrating to the XAD-7 resin on those filters which were in total contact with the resin, or the filter laying on top of the resin, than those with the filter beside the resin. The longer the samples were stored, the more of the catechol was adsorbed by the XAD-7 resin.(Table 4)
Table 4
Storage Study

Day % Recovered Light % Recovered Dark
GFF XAD-7 Total GFF XAD-7 Total

7 26.7 72.6 99.3 33.7 65.3 99.0
7 58.3 41.6 99.9 44.4 54.7 99.1
7 45.4 53.1 98.5 49.5 48.8 98.3
14 0.3 98.2 98.5 24.3 74.6 98.9
14 1.4 97.6 99.0 22.6 74.1 96.7
14 20.4 76.6 97.0 1.0 97.5 98.5
Average 98.7 Average 98.4
Overall Average 98.6



2.6. Precision

The precision was calculated using the area counts from six injections of each standard at concentrations of 0.0644 mg/mL (0.429 ppm), 0.320 mg/mL (2.13 ppm), 0.644 mg/mL (4.29 ppm), and 1.33 mg/mL (8.86 ppm) catechol in the desorbing solvent. The pooled coefficient of variation was 0.0105.(Table 5)
Table 5
Precision Study

Injection
Number 0.0644mg/mL 0.320mg/mL 0.644mg/mL 1.33mg/mL

1 1740 16279 42942 114630
2 1775 16018 43672 113338
3 1792 16124 43863 112695
4 1788 16380 43343 113710
5 1755 16325 42926 111274
6 1791 16165 43275 111157
Average 1774 16215 43337 112801
Standard ± 21.6 136 379 1379
Deviation
CV 0.0122 0.00839 0.00875 0.0122
Pooled CV 0.0105

where:
CV (Coefficient of Variable) =  standard deviation

average
Pooled CV =


A1(CV1)2 + A2(CV2)2 + A3(CV3)2 + A4(CV4)2

A1 + A2 + A3 + A4
A(1), A(2),A(3),A(4) = # of injections at each level
CVl, CV2, CV3, CV4 = Coefficients at each level

2.7. Air volume and sampling rate studied
2.7.1. The air volume studied is 100 liters.

2.7.2. The sampling rate studied is 1 liter per minute.
2.8. Interferences

Suspected interferences should be listed on sample data sheets.

2.9. Safety precautions
2.9.1. Sampling equipment should be placed on an employee in a manner that does not interfere with work performance or safety

2.9.2. Safety glasses should be worn at all times in designated areas.

2.9.3. Follow all safety practices that apply to the workplace being sampled.
3. Analytical method
3.1. Apparatus
3.1.1. Gas chromatograph equipped with a flame ionization detector. A HP 5890 gas chromatograph was used in this study.

3.1.2. GC column capable of separating the analyte and an internal standard from any interferences. The column used in this study was a 15 meter DB-WAX capillary column 0.25µ d.f., 0.32mm I.D.

3.1.3. An electronic integrator or some other suitable method of measuring peak areas.

3.1.4. Two and four milliliter vials with Teflon-lined caps.

3.1.5. A 10 µL syringe or other convenient size for sample injection.

3.1.6. Pipettes for dispensing the desorbing solution. The Glenco 1 mL dispenser was used in this method.

3.1.7. Volumetric flasks - 5 mL and other convenient sizes for preparing standards.

3.1.8. An analytical balance capable of weighing to the nearest 0.01 mg.
3.2 Reagents
3.2.1. Purified GC grade nitrogen, hydrogen, and air.

3.2.2. Catechol, Reagent grade

3.2.3. Methanol, HPLC grade

3.2.4. Dimethyl formamide, Reagent grade

3.2.5. The desorbing solution is 0.25 µL/mL dimethyl formamide in methanol.
3.3. Sample preparation
3.3.1. Sample tubes are opened and the glass fiber filter and the front and back section of each tube are placed in separate 4 mL vials.

3.3.2. Each section is desorbed with 3 mL of the desorbing solution.

3.3.3. The vials are sealed immediately and allowed to desorb for 30 minutes on a shaker, a roto-rack, or a sample rocker.

3.3.4. Samples were transfered to two milliliter vials for anaylsis, as this was the size needed to fit in the autosampler.
3.4. Standard preparation
3.4.1. Standards are prepared by diluting a known quantity of catechol with the desorbing solution.

3.4.2. At least two separate stock standards should be made. Dilutions of the stock standards are prepared covering the concentrations in the samples. The analytical standards used in this study ranged from 0.001 to 1.33 mg/mL of catechol the desorbing solution.
3.5. Analysis
3.5.1. Gas chromatograph conditions.

Flow rates (mL/min) Temperature (°C)
Nitrogen(makeup) : 30 Injector : 220
Hydrogen(carrier) : 1.5 Detector : 250
Air : 450 Column : 90°-1 min
Hydrogen(detector) : 60 15°C/min-220°C
Injection size : l µL
Elution time : 8.912 min
Chromatogram :(See Figure 2)


3.5.2. Peak areas are measured by an integrator or other suitable means.
3.6. Interferences (analytical)
3.6.1. Any compound having the general retention time of the analyte or the internal standard used is an interference. Possible interferences should be listed on the sample data sheet. GC parameters should be adjusted if necessary so these interferences will pose no problems.

3.6.2. Retention time data on a single column is not considered proof of chemical identity. Samples over the target concentration should be confirmed by GC/Mass Spec or other suitable means.
3.7. Calculations
3.7.1. A curve with area counts versus concentration is calculated from the calibration standards.

3.7.2. The area counts for the samples are plotted with the calibration curve to obtain the concentration of catechol in solution.

3.7.3. To calculate the concentration of analyte in the air sample the following formulas are used:

(µg/m)(desorption volume)
(desorption efficiency)
= mass of analyte in sample


(mass of analyte in sample)
molecular weight
= number of moles of analyte


(number of moles of analyte) (molar volume at 25°C & 760mm) = volume the analyte will occupy at 25°C & 760mm


(volume analyte occupies)(106)
(air volume)
= ppm


* All units must cancel.

3.7.4. The above equations can be consolidated to form the following formula. To calculate the ppm of analyte in the sample based on a 100 liter air sample:

(µg/mL)(DV)(24.45)(106)
(100 L)(DE)(MW)
× (g)
(1000 mg)
× (mg)
(1000 µg)
= ppm


µg/mL = concentration of analyte in sample or standard
24.45 = Molar volume (liters/mole) at 25 °C and 760 mm Hg.
MW = Molecular weight (g/mole)
DV = Desorption volume of 3 mL
100 L = 100 liter air sample
DE = Desorption efficiency


3.7.5. This calculation is done for each section of the sampling tube and the results added together.
3.8. Safety precautions
3.8.1. All handling of solvents should be done in a hood.

3.8.2. Avoid skin contact with all chemicals.

3.8.3. Wear safety glasses, gloves and a lab coat at all times.
4. Recommendations for further study

Collection studies need to be performed.
For problems with accessibility in using figures please contact the SLTC at (801) 233-4900.
Figure 1. A diagram of an OVS-7 tube.



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

Figure 2. An analytical standard of 0.743 mg/mL catechol in methanol
with 0.25 µL/mL dimethyl formamide internal standard.


5. References
5.1. Cummins,K., Method 32, "Phenol and Cresol", Organic Methods Evaluation Branch, OSHA Salt Lake Technical Center, 1986.

5.2. Windholz, M., "The Merck Index", Eleventh Edition, Merck & Co., Rahway N.J., 1989, p.1272.

5.3. "Documentation of the Threshold Limit Values and Biological Exposure Indices", Fifth Edition, American Conference of Governmental Industrial Hygienists Inc., Cincinnati, OH, 1986, p. 112.