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Data bank of environmental chemicals     |     The Finnish Environment Institute (SYKE)
 


27.4.2024

Data bank of environmental properties of chemicals


Chemical
Hydroquinone
CAS-number :
123-31-9
 
Synonyms :
1,4-Benzenediol
1,4-dihydroksibentseeni
1,4-dihydroxybenzene
hydrokinoni
p-hydroksifenoli
p-hydroxyphenol
 
Sumformula of the chemical :
C6H6O2
EINECS-number :
2046178
 
Uses :
Photographic developer and oxidation inhibitor; dye
intermediate; medicine; inhibitor of polymerization.
 
State and appearance :
Hexagonal prisms. 
Light-tan, light-gray or colorless crystals.
 
Odor :
Sweet taste.
 
Molecular weight :
110.12
 
Spesicif gravity (water=1) :
1.3  at 20 °C
 
Vapor pressure, mmHg :
150°C
0.0000015  at 24 °C, IUCLID 1996
0.00067  at 25 °C, estrapolated, HSDB 1999
 
Water solubility, mg/l :
70000  25°C
58000  MITI 1992
 
Melting point, °C :
172 
169  169 - 171 °C, IUCLID 1996
171 
 
Boiling point, °C :
285  285 - 287 °C, IUCLID 1996
287 
 
Flashing point, °C :
165  closed cup, IUCLID 1996
 
pKa :
10.85  at 25 °C, HSDB 1999
 
Log octanol/water coefficient, log Pow :
0.5  IUCLID 1996
0.59  HSDB 1999
 
Volatilization :
The Henry's Law constant was estimated from the vapor pressure 
(1.9x10-5 mmHg at 25 °C) and the water solubility (72 g/l 25°C)
and it is 3.84x10-11 atm m3/mol. 
The vapor pressure and the 
Henry's Law constant indicate that significant volatilization 
from dry and moist soil is not expected (IUCLID 1996).

Hydroquinone is not expected to volatilize from water based on 
this estimated value of the Henry's Law constant (HSDB 1999).
 
Adsorption/desorption :
An estimated Koc is 9 to 50 (IUCLID 1996).
 
Mobility :
The Koc-values indicate that hydroquinone has a very low 
capability to adsorb and will display high to very high 
mobility in soil (IUCLID 1996).
 
Other physicochemical properties :
Very soluble in carbon tetrachloride.
 
Photochemical degradation in air :
Photooxidation half-life in air:
26.1hr - 2.6hr, scientific judgement based upon an estimated
rate constant for vapor phase reaction with hydroxyl radicals
in air (Howard 1991).

If hydroquinone is released to the atmosphere, it is expected 
to undergo direct photochemical degradation. 

Direct photolysis:
57 % after 17 hr (measured) at 15 °C, light spect. 290 nm
The mineralization is calculated as the percentage CO2 to the 
theorical possible carbon dioxide (IUCLID 1996).

An estimated rate constant for the gas-phase reaction of 
hydroquinone with photochemically produced hydroxyl radicals of 
2.3x10-11 cm3/molc-sec translates to a half-life of 16.8 hr 
using an average atmospheric hydroxyl radical concn of 5x10+5 
molc/cm3 (HSDB 1999).
 
Photochemical degradation in water :
Photooxidation half-life in water:
19.3hr - 23min, scientific judgement based upon measured rate 
data for alkylperoxyl radicals in aqueous solution (Howard 
1991).
 
Half-life in air, days :
1.09  26.1hr - 2.6hr.
0.11  scientific judgement based upon estimated photooxidation halr-life in air.
  Howard 1991
 
Half-life in soil, days :
7d - 1d,
scientific judgement based upon estimated unacclimated aqueous aerobic biodegradation half-life.
  Howard 1991
 
Half-life in water, days :
0.8  19.3hr - 0.39hr,
0.02  in surface water: based upon photooxidation half-life in water.
14  14d - 2d,
in ground water: scientific judgement based upon estimated unacclimated aqueous aerobic biodegradation half-life.
  Howard 1991
 
Aerobic degradation in water :
Aerobic half-life:
7d - 1d, scientific judgement based upon aqueous screening test
data (Howard 1991).

Biodegradation:
concentration: 50 mg/l related to DOC
degradation: 86 % after 14 d
readily biodegradable (OECD 301 C)
(IUCLID 1996).

Biodegradation:
concentration: 2 mg/l related to DOC
degradation: 81 % after 30 d
readily biodegradable (OECD 301 D)
(IUCLID 1996).

Biodegradation:
concentration: 400 mg/l related to DOC
degradation: 66 % after 14 d
inherent biodegradability (OECD 302 B)
(IUCLID 1996).
 
Anaerobic degradation in water :
Anaerobic half-life:
28d - 4d, scientific judgement based upon estimated 
unacclimated aqueous aerobic biodegradation half-life (Howard 
1991).
 
Total degradation in water :
Biodegradation:
70% by BOD
period: 14d
substance: 100 mg/l
sludge: 30 mg/l
(MITI 1992)
 
Ready biodegradability :
Confirmed to be biodegradable (Anon. 1987).
 
Bioconcentration factor, fishes :
40  3d, at 23 °C, Leuciscus idus melanotus,
  conc. 0.05 mg/l, IUCLID 1996
 
Other information of bioaccumulation :
Bioconcentration factor (algae):
40 - 65, 1d, Chlorella fusca, conc. 0.05 mg/l
(IUCLID 1996).
 
LD50 values to mammals in oral exposure, mg/kg :
320  orl-rat, Lewis & Sweet 1984
70  orl-cat, - " -
 
LD50 values to mammals in non-oral exposure , mg/kg :
5970  skn-mam, Lewis & Sweet 1984
 
LD50 values to birds in oral exposure, mg/kg :
300  orl-pgn, Lewis & Sweet 1984
 
Effects on microorganisms :
Toxicity threshold (cell multiplication inhibition test):
bacteria (Pseudomonas putida): 58 mg/l
(Bringmann & Kühn 1980a)
 
EC50 values to algae, mg/l :
13.5  5 d, Scenedesmus subspicatus
0.335  3 d, Selenastrum capricornutum
  IUCLID 1996
 
LOEC values to algae, mg/l :
0.93  Scenedesmus quadricauda, Bringmann &
  Kühn 1980a
  --
7 d, Selenastrum capricornutum, IUCLID 1996
 
NOEC values to algae, mg/l :
0.4  7 d, Selenastrum capricornutum, IUCLID 1996
 
LC50 values to crustaceans, mg/l :
0.05  48 hr, Daphnia magna, Könemann 1979
 
EC50 values to crustaceans, mg/l :
0.29  48 hr, Daphnia magna
0.16  48 hr, Daphnia pulicaria
0.12  24 hr, Daphnia magna
  IUCLID 1996
  --
0.13  48 hr, Daphnia magna
0.16  48 hr, Daphnia pulicaria
  IUCLID 1996
 
LC50 values to fishes, mg/l :
0.097  96 hr, Salmo gairdneri, DeGraeve et al.
  1980
0.044  96 hr, Pimephales promelas, - " -
  --
0.17  96hr, Branchydanio rerio
0.16  48hr, Leuciscus idus, Wellens 1982
  --
0.044  96 hr, Pimephales promelas
0.639  96 hr, Salmo gairdneri, OECD 203
0.097  96 hr, Salmo gairdneri
0.17  96 hr, Brachydanio rerio
  IUCLID 1996
  --
0.044  0.044 - 0.097 mg/l, 96 hr, Oncorhynchus mykiss
0.097  AQUIRE 1999
 
Other information of water organisms :
Daphnia pulex: 0.001 mol/l, srv, 0.07 days (Stom et al. 1986). 
Toxicity threshold (cell multiplication inhibition test):
green algae (Scenedesmus quadricauda): 0.93 mg/l
protozoa (Entosiphon sulcatum): 11 mg/l
(Bringmann & Kühn 1980a)

References
1848Anon. 1987a. The list of the existing chemical substances tested on biodegradability by microorganisms or bioaccumulation in fish body by Chemicals Inspection & Testing Institute. Ministry of International Trade and Industry, MITI. Japan.
3107AQUIRE 1993 -. Aquatic Toxity Information Retrieval Database. U.S.Environmental Protection Agency, Office of Pesticides and Toxic Substances, Washington, D.C.
188Bringmann, G. & Kühn, R. 1980a. Comparison of the toxicity thresholds of water pollutants to bacteria, algae and protozoa in the cell multiplication inhibition test. Water Res. 14: 231 - 241.
331DeGraeve, G.M. et al. 1980. Toxicity of underground coal gasification condenser water and selected constituents to aquatic biota. Arch. Environ. Contam. Toxicol. 9: 543.
330DeGraeve, G.M., Geiger, D.L., Meyer, J.S. & Bergman, H.L. 1980. Acute and embryo-larval toxicity of phenolic compounds to aquatic biota. Arch. Environ. Contam. Toxicol. 9: 557 - 568.
3120Howard, P.H., Boethling, R.S., Jarvis, W.F., Meylan, W.M. & Michalenko, E.M., Handbook of Environmental Degradation Rates, 1991. Lewis Publicers, Inc., Chelsea, Michigan, U.S.A., pp. 725.
3114HSDB Database 1992 -. Hazardous Substances Data Bank. US. National Library of Medicine. TOMES Plus CD-ROM.
3253IUCLID 1995 -. International Uniform Chemical Information Database. European Commission. European Chemicals Bureau. Existing Chemicals. Ispra, Italy.
761Könemann, W.H. 1979. Quantitative structure-activity relationships for kinetics and toxicity of aquatic pollutants and their mixtures in fish. Univ. Utrecht, Netherlands.
1589Lewis, R.J. & Sweet, D.V. 1984. Registry of toxic effects of chemical substances. National Institute for Occupational Safety and Health. No. 83-107-4.
3105MITI 1992. Biodegradation and bioaccumulation data of existing chemicals based on the CSCL Japan. Compild under the Safety Division Basic Industries Bureau Ministry of International Trade & Industry, Japan. Edited by Chemicals Inspection & Testing Institute, Japan.
1927Stom D.J. et al. 1986. Effect of individual phenolic compounds and of their mictures on luminous bacteria. Part 3. Combined action of phenolic compounds on aquatic organisms. Acta Hydrochim. Hydrobiol. 14: 539.
1531Wellens, H. 1982. Comparison of the sensitivity of Branchydanio rerio and Leucistus idus by testing the fish toxicity of chemicals and wastewaters. Z. Wasser Abwasser Forsch. (Ger.) 15: 49.

 
 
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