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Annex III Entry 27 14/05/2013

Sodium monofluorophosphate

Sodium monofluorophosphate is listed in Annex III and may only be used under the conditions shown in this record. Maximum concentration in this record: 0.15% calculated as F. When mixed with other fluorine compounds permitted under this Annex, total F concentration must not exceed 0.15%.

Restricted substance— Annex III, EU Regulation 1223/2009
Max conc.: 0.15%
Entry: 27

Chemical identity and properties

PubChem 2D chemical structure for CAS 10163-15-2
CAS 10163-15-2CAS 7631-97-2PubChem CID 24266

Sodium Monofluorophosphate

Sodium fluorophosphate, commonly abbreviated MFP, is an inorganic compound with the chemical formula Na2PO3F. Typical for a salt, MFP is odourless, colourless, and water-soluble. This salt is an ingredient in toothpastes. It has a role as an antibacterial agent. It is an inorganic phosphate and an inorganic sodium salt. ChEBI

IUPAC name
disodium;fluoro-dioxido-oxo-lambda5-phosphane
Molecular formula
FNa2O3P
Molecular weight
143.950 g/mol
Exact mass
143.93644758 Da
Topological polar surface area
63.2 Ų
Hydrogen-bond donors
0
Hydrogen-bond acceptors
4
Covalent units
3
Defined stereocentres
0

Also known as

Phosphorofluoridic acid, disodium saltExtra-Strength AimC810JCZ56QNSC-248bridentsmilecareRegularRembrandt
16 more reported names
SaliveaBarbieOrazenPriyalSparkleFreshMyntSmilepurple toothSmartMouthAGToothpasteCloveden ToothDeCureFinefra SilverGlancure ToothHello WhiteningKroger CompanyNatures Promise
External database identifiers

Evidence from additional scientific databases

EMBL-EBI ChEBI
Exact identifier matchCHEBI:86431

sodium fluorophosphate

Sodium fluorophosphate, commonly abbreviated MFP, is an inorganic compound with the chemical formula Na2PO3F. Typical for a salt, MFP is odourless, colourless, and water-soluble. This salt is an ingredient in toothpastes.

Formula
FO3P.2Na
Average mass
143.949 g/mol
Monoisotopic mass
143.93645 Da
Formal charge
0
  • inorganic sodium salt — is a (CHEBI:38702)
  • inorganic phosphate — is a (CHEBI:24838)
  • antibacterial agent — has role (CHEBI:33282)
  • antibacterial agent — has role (CHEBI:33282)
  • inorganic sodium salt — is a (CHEBI:38702)
  • inorganic phosphate — is a (CHEBI:24838)
Additional curated names
disodium phosphorofluoridatedisodium fluorophosphatedisodium monofluorophosphateNSC-248Phosphorofluoridic acid, disodium saltSodium fluorophosphatesodium monofluorophosphateSodium phosphorofluoridate
Cross-references from this source

Mapped by: Exact CAS cross-reference in the ChEBI compound record. Source updated: 2015-07-24. Retrieved: 2026-08-31. Open source record

NIH PubChem PUG-View
Exact identifier match24266

Attributed physical-property, hazard, environmental and use annotations.

  • Note: This chemical does not meet GHS hazard criteria for 1.4% (1 of 72) of reports. Source: European Chemicals Agency (ECHA)
  • Signal: Warning Source: European Chemicals Agency (ECHA)
  • GHS Hazard Statements: H302 (91.7%): Harmful if swallowed [Warning Acute toxicity, oral]; H315 (11.1%): Causes skin irritation [Warning Skin corrosion/irritation] Source: European Chemicals Agency (ECHA)
  • Precautionary Statement Codes: P264, P270, P280, P301+P317, P302+P352, P321, P330, P332+P317, P362+P364, and P501 (click each P-code to see the statement) Source: European Chemicals Agency (ECHA)
  • ECHA C&L Notifications Summary: Aggregated GHS information provided per 72 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.; Reported as not meeting GHS hazard criteria per 1 of 72 reports by companies.; There are 4 notifications provided by 71 of 72 reports by companies with hazard statement code(s).; Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website. Source: European Chemicals Agency (ECHA)
  • GHS Hazard Statements: H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]; H312 (100%): Harmful in contact with skin [Warning Acute toxicity, dermal]; H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]; H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]; H332 (100%): Harmful if inhaled [Warning Acute toxicity, inhalation]; H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation] Source: European Chemicals Agency (ECHA)
  • Precautionary Statement Codes: P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement) Source: European Chemicals Agency (ECHA)
  • ECHA C&L Notifications Summary: Aggregated GHS information provided per 8 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.; Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website. Source: European Chemicals Agency (ECHA)

Mapped by: Existing checksum-valid CAS to unique PubChem CID match. Retrieved: 2026-08-31. Open source record

Scientific classifications and hazard annotations provide context and do not replace the market-specific regulatory decision shown above.

Additional source coverage and match status
SourceResultChecked
EMBL-EBI ChEBIExact match2026-08-31
NIH PubChem PUG-ViewExact match2026-08-31

A recorded no-match is useful evidence that the source was checked; it is not a claim that the substance does not exist elsewhere.

Retrieved from NIH PubChem on 2026-09-02 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.

Record details

Maximum concentration

0.15% calculated as F. When mixed with other fluorine compounds permitted under this Annex, total F concentration must not exceed 0.15%

Product type

Warnings

Contains sodium monofluorophosphate
For any toothpaste with compounds containing fluorine in a concentration of 0.1 to 0.15% calculated as F unless it is already labelled as contra-indicated for children (e.g. "for adult use only") the following labelling is obligatory:
"Children of 6 years and younger: use a pea-sized amount for supervised brushing to minimise swallowing. In case of intake of fluoride from other sources consult a dentist or doctor."

Chemical name

Sodium monofluorophosphate

Chemical / IUPAC name

Disodium fluorophosphate

Regulatory information

Key data

CAS
10163-15-2 -- 7631-97-2
EC
233-433-0 -- 231-552-2
Annex
Entry number
27

Inventory links for Sodium monofluorophosphate

What Annex III means for Sodium monofluorophosphate

Sodium monofluorophosphate is a restricted substance under Annex III of EU Cosmetics Regulation 1223/2009. Its use in cosmetics is only permitted under the specific conditions set out in the entry above, including applicable concentration limits, product type restrictions and required warning statements.

When including this substance in a formulation, all conditions — maximum concentration, product scope and warning labels — must be met simultaneously. Compliance with one condition does not override the others.

This record is linked to 1 CosIng inventory ingredient for name and identifier cross-reference. The page also surfaces 12 related annex records with overlapping identifiers, annex logic or naming patterns.

Compliance checklist

  • Ensure formulation concentration does not exceed: 0.15% calculated as F. When mixed with other fluorine compounds permitted under this Annex, total F concentration must not exceed 0.15%
  • Confirm product type compatibility: Oral products
  • Include required warning statement on product label.
  • Document conditions of use in the Product Information File (PIF).

Frequently asked questions

Sodium monofluorophosphate is listed in Annex III of EU Regulation 1223/2009 as a restricted substance. It may only be used under the conditions specified in the entry, including any maximum concentration, product type limitation and required warning statements shown above.

CAS 10163-15-2 -- 7631-97-2 is the unique numerical identifier assigned to Sodium monofluorophosphate by the Chemical Abstracts Service. In cosmetic compliance work, the CAS number is used to cross-reference the substance across regulatory databases, raw material specifications and safety assessment reports. Multiple EU annex entries may share the same CAS number if the same substance appears under different conditions or in different annexes.

The maximum concentration of 0.15% calculated as F. When mixed with other fluorine compounds permitted under this Annex, total F concentration must not exceed 0.15% applies to the concentration of the substance in the ready-to-use cosmetic product. When the substance is supplied as part of a blend or mixture, the calculation must account for the contribution of all sources in the formulation. The combined concentration must not exceed the stated limit.

Use the INCI Checker tool on this site to paste your full ingredient list (INCI) and scan it against all Annex II–VI entries. The tool highlights any ingredients that match restricted, prohibited or allergen-flagged records. This is useful for rapid compliance screening of finished product formulas or raw material declarations.

Source note for Annex III record Sodium monofluorophosphate

This page summarizes one Annex III record for Sodium monofluorophosphate from public European Commission cosmetic materials and adds linked inventory or identifier matches when available.

Use this record page to review Annex III conditions for Sodium monofluorophosphate, but confirm any final regulatory decision against the current official annex wording and source files.

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