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
2 study endpoints found for Xylose. 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 | 15000 mg/kg bw/day | oral | rat | Subchronic | COSMOS_DB |
| NOAEL | >5 other | oral | rat | oral | REACH |
Expert Verdict
None significant; clean ingredient with long safety history
Regulatory Flags
Frequently Asked Questions
Is Xylose safe in cosmetics?
None significant; clean ingredient with long safety history The EU classifies Xylose as "permitted". Safety rating: EXCELLENT. 2 toxicological study endpoint(s) are available in our database.
Is Xylose allowed in the EU?
Xylose EU regulatory status: permitted. This is based on EU Regulation 1223/2009 and its amendments.
What does Xylose do in cosmetics?
Xylose functions as: Skin conditioning agent, humectant, flavoring agent. It is classified as a cosmetic ingredient in our database. CAS number: 58-86-6.
What is the Margin of Safety for Xylose?
not established 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 Xylose?
The NOAEL (No Observed Adverse Effect Level) for Xylose is 15000 mg/kg bw/day based on a Subchronic study via oral route in rat. A total of 2 study endpoints are available. Source: COSMOS_DB.
Compliance Tools
Check Xylose compliance across multiple jurisdictions:
Related Ingredients
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