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Dipropylene glycol (SIDS)

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OECD <strong>SIDS</strong><br />

DIPROPYLENE GLYCOLE<br />

5. Conclusions and Recommendations<br />

5.1 Conclusions<br />

Commercial dipropylene <strong>glycol</strong> (CAS # 25265-71-8; (CH3-CHOH-CH2O-CH2-CHOH-<br />

CH3) is composed of 3 isomers and is typically 98% pure. The commercial product is<br />

typically composed of up to 48% isomer 110-98-5. <strong>Dipropylene</strong> <strong>glycol</strong> is produced as a<br />

byproduct of the manufacture of propylene <strong>glycol</strong>. The US production capacity of<br />

dipropylene <strong>glycol</strong> was 131 million pounds (60 thousand tonnes) in 1998. <strong>Dipropylene</strong><br />

<strong>glycol</strong> is used as both a reactive intermediate and as a solvent. Reactive intermediate end<br />

uses in the US include: plasticizers, unsaturated polyester resins, polyurethane polyols,<br />

and alkyd resins. Solvent end uses in the US include: cosmetics, pesticides and functional<br />

fluids: specialty deicers, inks, lubricants.<br />

<strong>Dipropylene</strong> <strong>glycol</strong> is a liquid at room temperature, it has a low vapor pressure, and is<br />

miscible with water. Releases to the environment are expected to partition primarily to<br />

water and soil where they will be degraded. It is not expected to bioaccumulate due to<br />

BCFs measured at 0.3 to 4.6. Testing in aquatic species showed a low hazard concern.<br />

PNECs of >50 mg/L were obtained from a fish LC 50 of 5000 mg/l and 32 mg/l from a<br />

clawed toad (Xenopus laevis) LC 50 of 3181 mg/l. The mammalian acute toxicity of<br />

dipropylene <strong>glycol</strong> is low, with values around 16000 mg/kg reported in tests in rats.<br />

<strong>Dipropylene</strong> <strong>glycol</strong> is only minimally irritating to the skin and eye. It appears to have low<br />

potential to produce allergic skin reactions, as only 1 of 503 patients with eczema reacted<br />

to dipropylene <strong>glycol</strong>. Longer-term studies of dipropylene <strong>glycol</strong> and the structural<br />

analogues, propylene <strong>glycol</strong> and tripropylene glcyol, demonstrate a low concern for<br />

chronic, reproductive, and developmental effects. <strong>Dipropylene</strong> <strong>glycol</strong> is not genotoxic<br />

and not expected to be carcinogenic.<br />

5.2 Recommendations<br />

The chemical is currently a low priority for further work.<br />

18<br />

UNEP PUBLICATIONS

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