LINEAR ALKYLBENZENE SULFONATE (LAS) - UNEP Chemicals
LINEAR ALKYLBENZENE SULFONATE (LAS) - UNEP Chemicals
LINEAR ALKYLBENZENE SULFONATE (LAS) - UNEP Chemicals
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OECD SIDS <strong>LINEAR</strong> <strong>ALKYLBENZENE</strong> <strong>SULFONATE</strong> (<strong>LAS</strong>)<br />
2) Tiba, S. 1972. Studies on the acute and chronic toxicity of linear<br />
alkylbenzene sulfonate. J. Food Hyg. Soc. Jpn. 16:66-71 (in Japanese); cited<br />
in: IPCS (1996); Environmental Health Criteria 169: Linear Alkylbenzene<br />
Sulfonates (<strong>LAS</strong>) and Related Compounds. WHO, Geneva, Switzerland.<br />
Reliability: 4 This study is assigned a reliability score of 4 because the original report<br />
was not available for review. However, the study was evaluated by IPCS<br />
prior to inclusion in their criteria document<br />
(c)<br />
Species/strain: Rat/Wistar<br />
Sex: Female [ ]; Male [ ]; Male/Female [X]; No data [ ]<br />
Administration: drinking water<br />
Exposure period: up to 26 months<br />
Frequency of treatment: Daily<br />
Doses: 0.1% (140 mg/kg bw d)<br />
Control group: Yes [X]; No [ ]; No data [ ];<br />
Concurrent no treatment [ ]; Concurrent vehicle [ ]; Historical [ ]<br />
Results: The administration of <strong>LAS</strong> had no effect on the intake of water, mortality,<br />
body weight gain, or general condition. In pathological examination,<br />
looseness, atrophy, and fatty change of the hepatic cells in the liver were<br />
found in the experimental group at 6 months. The experimental group<br />
showed significant increases in GOT, GTP and bilirubin at 6 months and<br />
thereafter. In haematological examinations no effects due to <strong>LAS</strong> were<br />
observed.<br />
Method: A group of 62 male and 62 female rats were given drinking water treated<br />
with <strong>LAS</strong> and a control group of 37 male and 37 female rats were given pure<br />
water. Five to 12 of the rats in the experimental group and 3 to 12 rats in the<br />
control group at 3, 6, 12, and 18 months, respectively, and all surviving rats<br />
between 24 and 26 months, were sacrificed for pathological, biochemical,<br />
and haematological examinations.<br />
GLP: Yes [ ] No [X] ? [ ]<br />
Test substance: <strong>LAS</strong>; mean molecular weight 348; average alkyl chain length = C12.0;<br />
activity: 38.74%<br />
Remarks: Information as cited in the IPCS document.<br />
Reference: 1) European Commission. 2000a. Benzenesulfonic acid, C10-13-alkyl derivs.,<br />
sodium salts. Year 2000 CD-ROM edition.<br />
2) Endo, T., Furuido, Y., Namie, K., Yamamoto, N., Hasunuma, H. and<br />
Ueda, K. 1980. Studies of the chronic toxicity and teratogenicity of<br />
synthetic surfactants. Ann. Rep. Tokyo Metrop. Res. Inst. Environ. Prot.<br />
236-246 (in Japanese); cited in: IPCS (1996); Environmental Health Criteria<br />
169: Linear Alkylbenzene Sulfonates (<strong>LAS</strong>) and Related Compounds.<br />
WHO, Geneva, Switzerland.<br />
Reliability: 4 This study is assigned a reliability score of 4 because the original report<br />
was not available for review. However, the study was evaluated by IPCS<br />
prior to inclusion in their criteria document.<br />
(d)<br />
Species/strain: Rat/Wistar<br />
Sex: Female [ ]; Male [ ]; Male/Female [X]; No data [ ]<br />
Administration: oral feed<br />
Exposure period: 1, 3, 6, 24, or more months<br />
Frequency of treatment: Daily<br />
Doses: 0.04, 0.16, 0.6% (20, 80, 300 mg/kg bw d)<br />
Control group: Yes [X]; No [ ]; No data [ ];<br />
Concurrent no treatment [X]; Concurrent vehicle [ ]; Historical [ ]<br />
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