| Many manufacturers 
              and distributors of so-called natural and/or organic personal care 
              products claim to have made an informed choice to use Cocamidopropyl 
              betaine (CAPB) rather than Sodium lauryl ether sulphate (SLES) as 
              a foaming agent in their products, are often disparaging of their 
              competitors use of SLES and usually fraudulently miscontextualise 
              or even fabricate misinformation regarding the safety of SLES. Cocamidopropyl 
              betaine (CAPB) is an non-ionic, amphoteric surfactant, foaming agent 
              and emulsifier used in the formulation of rinse-off shampoos, liquid 
              soaps, gels and cosmetic and household cleansers due to its reputation 
              as being a milder (less irritating) agent than most older and many 
              contemporary alternatives, including Sodium lauryl ether sulphate 
              (SLES), especially from the point of view of being less stinging 
              to the eyes.  Made from coconut oil, with petrochemical 
              ingredients, Cocamidopropyl betaine is a quasi-natural substance, 
              as is SLES. Being notably milder to the eyes quickly led to its 
              preferential use in baby shampoos and to manufacturers claiming 
              their product to be milder and safer than that of their competitors 
              who were using Sodium laureth sulphate/Sodium lauryl ether sulphate 
              (SLES). This in turn led to consumer advocates, doctors, consumers 
              and patients assuming that a less irritating product such as a baby 
              shampoo would be safer for the skin, causing more to formulate with, 
              recommend and to seek out CAPB based products over those containing 
              SLES. Cocamidopropyl betaine is a tamed version of a harsher older 
              surfactant, Cocamide DEA, as is Sodium Lauryl Ether Sulphate (SLES) 
              a tamed version of the harsher older Sodium Lauryl Sulphate (SLS). Cocamidopropyl betaine does however have 
              a dark side that surfaced along with increasing consumer usage, 
              namely its identification and confirmation as a contact allergen, 
              something that Sodium lauryl ether sulphate (SLES) is not. Furthermore, 
              like SLES, which its detractors, based on its early manufacturing 
              standards and also current industrial grades, but not necessarily 
              in its modern cosmetic grade incarnation, point out, Cocamidopropyl 
              betaine contains several allergenic impurities including carcinogenic 
              nitrosamines, (Haz-Map, Natl Inst 
              Health, USA, 20 July, 2004), making a double mockery 
              of SLES-critical manufacturer's claims of a better safety profile 
              for CAPB. Since its introduction, Cocamidopropyl betaine been increasingly 
              revealed, like SLES, to be a skin sensitizer, but moreover, unlike 
              SLES, CAPB has increasingly been identified as a significant cause 
              of allergic contact dermatitis, to the extent of being voted Contact 
              Allergen of the year for 2004 by a committee of international experts 
              (Mowad C, Adv Dermatol, 20:237, 2004). 
               With reports of confirmed allergenic dermatitis 
              caused by Cocamidopropyl betaine having first been recorded more 
              than a decade ago, CAPB is now unquestionably documented and acknowledged 
              as one of the most frequent (SLES does not even feature) causes 
              of dermatitis of the head, neck and face in humans and especially 
              so of the eyelids and lips of infants, where its use can lead to 
              intractable inflammation and scaling (Korting 
              H et al, J Am Acad Dermatol, 27(6 Pt 1), 1992); (Peter C et al, 
              Contact Dermatitis, 26(4), 1992); (Taniguchi S et al, Contact Dermatitis, 
              26(2), 1992); (Fowler J, Cutis, 52(5), 1993); (Angelino G et al, 
              Contact Dermatitis, 32(2), 1995); (de Groot A, et al, Contact Dermatitis, 
              33(6), 1995); (de Groot A, Clin Dermatol, 15(4), 1997); (Angelini 
              D et al, Contact Dermatitis, 39(4), 1998); (Brand R et al, Australas 
              J Dermatol, 39(2), 1998); (Lin-Hui S et al, Contact Dermatitis, 
              38(3), 1998); (Armstrong D et al, Contact Dermatitis, 40(6), 1999); 
              (Krasteva M et al, Europ J Dermatol, 9 (2), 1999); (Yasunaga C et 
              al, Environ Dermatol, 7(1), 2000); (Hashimoto R et al, Environ Dermatol, 
              7(2), 2000); (Mowad C, Am J Contact Dermatitis, 12(4), 2001); (McFadden 
              J et al, Contact Dermatitis, 45(2), 2001); (Foti C et al, Contact 
              Dermatitis, 48: 194, 2003); (Moreau L et al, Dermatitis, 15(3), 
              2004); (Goosens A, Bull Soc Belge Ophtalmol, 292, 11, 2004); (Brey 
              N et al, Dermatitis, 15(1), 2004); (Fowler J et al, Am J Dermatol 
              (15(1), 2004); (Shaffer K, 15th Ann Meet Am Contact Dermatitis Soc, 
              Wash, 5 Feb, 2004); (Agar N et al, Australas J Dermatol, 46(1), 
              2005); (Bloom M, Recognising contact dermatitis, Dermatol Times, 
              June, 2005).
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