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 />
Reference: Debane, C. 1978. National Hygiene Laboratory; in: "Report on Studies on<br />
Synthetic Detergents", October 1978, Japan's Science and Technology<br />
Agency [in Japanese].<br />
Reliability: 4 Not assignable<br />
(b)<br />
Type: Toxicokinetics<br />
Method: The absorption, distribution, metabolism and elimination of <strong>LAS</strong><br />
(radioactively labelled with 35 S) were studied in male Charles River rats.<br />
<strong>LAS</strong> was administered as an aqueous solution.<br />
Results: The compound was readily absorbed from the gastrointestinal tract (80-90%<br />
of the dose). Most of the absorbed 35 S was eliminated within 72 hours and<br />
60-65% of the absorbed dose was eliminated in the urine, with sulfophenyl<br />
butanoic and sulfophenyl pentatonic acid as metabolites. These metabolites<br />
were not reabsorbed from the kidney tubules. 35% of the absorbed 35 S was<br />
excreted in the bile and were reabsorbed completely from the gastrointestinal<br />
tract. Although the metabolites in the bile were not identified, it was shown<br />
that no unchanged <strong>LAS</strong> was eliminated via this pathway.<br />
Test substance: C10-13, <strong>LAS</strong> (CAS #68411-30-3); alkyl chain length predominately C11, C12<br />
and C13.<br />
Remarks: The authors suggested that metabolism proceeded via omega oxidation with<br />
subsequent beta-oxidation. Retention of radioactivity was not observed in<br />
any organ.<br />
Reference: Michael, W.R. 1968. Metabolism of linear alkylate sulfonate and alkyl<br />
benzene sulfonate in albino rats. Toxicol. Appl. Pharmacol. 12:473-485.<br />
Reliability: 2 Valid with restrictions<br />
(c)<br />
Type: Toxicokinetics<br />
Results: <strong>LAS</strong> is well absorbed by via the gastrointestinal tract of pigs treated with 3.3<br />
mmol/animal 35S-Na-dodecylbenzene sulfonate. At 200 hours after oral<br />
administration, the radioactivity was relatively high in bristles and bones,<br />
while low in liver, kidney and spleen. After 10 weeks only traces of<br />
radioactivity were still in the body. 40 hours after the administration, 40% of<br />
the dose was excreted into the urine and 60% of the dose via the faeces.<br />
Remarks: Information as cited in the IUCLID Data Sheet and 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) Havermann, H. and Menke, K.H. 1959. Biological study of the watersoluble<br />
surface-active substances. Fette. Seifen. Anstrichmittel 61:429-434.<br />
(in German); cited in IPCS. 1996. Environmental Health Criteria 169:<br />
Linear Alkylbenzene Sulfonates and Related Compounds. World Health<br />
Organization, Geneva, Switzerland. Original article in Japanese.<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 />
Type: Toxicokinetics<br />
Results: Four (2 male, 2 female; 5 kg average body weight) adult rhesus monkeys<br />
(Macaca mulatta) were given single or repeated oral (30, 150 or 300 mg/kg)<br />
or subcutaneous (0.1, 0.5 or 1 mg/kg) doses of 14 C-<strong>LAS</strong>. After single 30<br />
mg/kg oral doses the radioactivity was rapidly excreted, mostly during the<br />
first 24 hours. Means of 71.2% and 23.1% of the dose were excreted in the<br />
urine and feces, respectively, during 5 days. Similarly, after single 1 mg/kg<br />
subcutaneous doses, means of 64.1% and 10.9% were excreted in urine and<br />
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