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Mexico, DF, June 29, 2005 Secretariat for the Stockholm Convention ...

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UNEP/POPS/POPRC.1/INF/8<br />

2. INFORMATION REQUIREMENTS AND SCREENING CRITERIA IN ANNEX D<br />

2.1 Chemical identity<br />

Lindane (CAS number 58-89-9) is <strong>the</strong> common name <strong>for</strong> <strong>the</strong> gamma isomer of Hexachlorocyclohexane<br />

(HCH). It is one of <strong>the</strong> 8 isomers of 1,2,3,4,5,6-HCH, chemical <strong>for</strong>mula C 6 H 6 Cl 6 , and has a molecular weight<br />

of <strong>29</strong>0.83 grams. The eight isomers differ in <strong>the</strong>ir axial-equatorial positions of <strong>the</strong> chlorine atoms around <strong>the</strong><br />

ring (Willet, 1998). The structural <strong>for</strong>mula of lindane is shown in Figure 1.<br />

Fig.1. Structural <strong>for</strong>mula of 1,2,3,4,5,6-HCH and gamma-HCH.<br />

HCH<br />

gamma-HCH<br />

Lindane is a white crystalline solid, stable in light, heat, air, carbon dioxide and strong acids. HCH isomers<br />

are produced by photochemical chlorination of benzene and result in a product called technical–HCH (CAS<br />

number: 608-73-1). Technical-HCH contains mainly five isomers: alpha-HCH (53-70%) (CAS number: 319-<br />

84-6), beta-HCH (3-14%) (CAS number: 319-85-7), gamma-HCH (11-18%), delta-HCH (6-10%) and<br />

epsilon-HCH (3-5%). The mixture of isomers was largely used as an inexpensive insecticide, but as <strong>the</strong><br />

gamma isomer is <strong>the</strong> only isomer showing strong insecticidal properties, it is purified from <strong>the</strong> mixture and<br />

commercialized under <strong>the</strong> name lindane. Technical lindane (>99% purity) is obtained by methanol or acetic<br />

acid treatment of technical-HCH followed by fractional recrystallization.<br />

Trade names of lindane containing products according to FAO include <strong>the</strong> following:<br />

Agrocide<br />

Aparasin<br />

Arbitex<br />

BBH<br />

Ben-hex<br />

4

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