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Cocamidopropyl betaine

Lauramidopropyl betaine
Structural formula of lauramidopropyl betaine
Lauramidopropyl betaine, the major component of cocamidopropyl betaine
Names
IUPAC name
{[3-(Dodecanoylamino)propyl](dimethyl)ammonio}acetate
Other names
2-[(3-Dodecanamidopropyl)dimethylaminio]acetate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.057.308 Edit this at Wikidata
EC Number
  • 263-058-8
UNII
  • InChI=1S/C19H38N2O3/c1-4-5-6-7-8-9-10-11-12-14-18(22)20-15-13-16-21(2,3)17-19(23)24/h4-17H2,1-3H3,(H-,20,22,23,24) checkY
    Key: MRUAUOIMASANKQ-UHFFFAOYSA-N checkY
  • InChI=1/C19H38N2O3/c1-4-5-6-7-8-9-10-11-12-14-18(22)20-15-13-16-21(2,3)17-19(23)24/h4-17H2,1-3H3,(H-,20,22,23,24)
    Key: MRUAUOIMASANKQ-UHFFFAOYAL
  • CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O
  • CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC(=O)[O-]
  • [O-]C(=O)C[N+](CCCNC(=O)CCCCCCCCCCC)(C)C
Properties
C19H38N2O3
Molar mass 342.524 g·mol−1
Appearance Clear to slight yellow liquid[1]
Density 1.05 g/cm3
Melting point < −10 °C (14 °F; 263 K)[1]
Boiling point > 100 °C (212 °F; 373 K)[1]
Soluble[1]
Viscosity < 100 cP (30°C)[1]
Hazards
GHS labelling:
GHS09: Environmental hazard[1]
Warning[1]
H315, H319, H400[1]
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
1
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Cocamidopropyl betaine (CAPB) is a mixture of closely related organic compounds derived from coconut oil and dimethylaminopropylamine.[2] CAPB is available as a viscous pale yellow solution and it is used as a surfactant in personal care products and animal husbandry. The name reflects that the major part of the molecule, the lauric acid group, is derived from coconut oil. Cocamidopropyl betaine to a significant degree has replaced cocamide DEA.

  1. ^ a b c d e f g h "Cocoamidopropyl-Betaine-CAPB-SDS" (PDF). Acme-Hardesty. Archived (PDF) from the original on 26 May 2021. Retrieved 26 May 2021.
  2. ^ Christian Nitsch, Hans-Joachim Heitland, Horst Marsen, Hans-Joachim Schlüussler, "Cleansing Agents" in Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a07_137

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بيتاين بروبيل كوكاميد Arabic Kokamidopropyl betain Czech Cocoamidopropyl-Betaine German کوکامیدوپروپیل بتائین FA Bétaïne de cocamidopropyle French Cocamidopropylbetaïne Dutch Kokamidopropylobetaina Polish Кокамидопропилбетаин Russian Kokamidopropil betain SH Kokamidopropil betain SL

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