Lauramidopropyl Hydroxysultaine
Regulatory Status
For full compliance data across 55 jurisdictions, use the Substance Compliance tool.
Safety Data
Calculate MoS for your specific formulation with the MoS Calculator.
Toxicological Studies
1 study endpoint found for Lauramidopropyl Hydroxysultaine. NOAEL (No Observed Adverse Effect Level) values are used to calculate the Margin of Safety per SCCS methodology.
| Endpoint | Value | Route | Species | Study Type | Source |
|---|---|---|---|---|---|
| NOAEL | 0.5 other | oral | rat | oral | REACH |
Expert Verdict
DMAPA impurity must remain <3 ppm; CIR Panel urges manufacturers to minimize DMAPA content; ocular irritation predicted in vitro at higher concentrations (≥1.25%); generally mild and well-tolerated
Regulatory Flags
Frequently Asked Questions
Is Lauramidopropyl Hydroxysultaine safe in cosmetics?
DMAPA impurity must remain <3 ppm; CIR Panel urges manufacturers to minimize DMAPA content; ocular irritation predicted in vitro at higher concentrations (≥1.25%); generally mild and well-tolerated The EU classifies Lauramidopropyl Hydroxysultaine as "permitted". Safety rating: GOOD. 1 toxicological study endpoint(s) are available in our database.
Is Lauramidopropyl Hydroxysultaine allowed in the EU?
Lauramidopropyl Hydroxysultaine EU regulatory status: permitted. This is based on EU Regulation 1223/2009 and its amendments.
What does Lauramidopropyl Hydroxysultaine do in cosmetics?
Lauramidopropyl Hydroxysultaine functions as: Anti-static agent; Cleaning agent; Foamant; Softener and conditioner; Surfactant (surface active agent); Viscosity modifier. It is classified as a cosmetic ingredient in our database. CAS number: 13197-76-7.
What is the Margin of Safety for Lauramidopropyl Hydroxysultaine?
adequate The Margin of Safety (MoS) is calculated using SCCS methodology. A MoS above 100 is generally considered safe. Use the MoS Calculator tool to calculate MoS for your specific formulation and product category.
What is the NOAEL for Lauramidopropyl Hydroxysultaine?
The NOAEL (No Observed Adverse Effect Level) for Lauramidopropyl Hydroxysultaine is 0.5 other based on a oral study via oral route in rat. Source: REACH.
Compliance Tools
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Related Ingredients
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