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Details

Stereochemistry ACHIRAL
Molecular Formula 2F.Sn
Molecular Weight 158.723
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of STANNOUS FLUORIDE

SMILES

[F-].[F-].[SnH2++]

InChI

InChIKey=NKCWZXPMTVCPSF-UHFFFAOYSA-L
InChI=1S/2FH.Sn.2H/h2*1H;;;/q;;+2;;/p-2

HIDE SMILES / InChI

Molecular Formula F
Molecular Weight 18.9984032
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula Sn
Molecular Weight 120.726
Charge 2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including https://www.drugs.com/international/olaflur.html | https://www.ncbi.nlm.nih.gov/pubmed/15528912 | https://clinicaltrials.gov/ct2/show/record/NCT00268138 | https://www.old.health.gov.il/units/pharmacy/trufot/alonim/4872.pdf

Olaflur (amine fluoride 297, trade name elmex gel) is a fluoride-containing substance that is an ingredient of toothpastes and solutions for the prevention of dental caries. Especially in combination with dectaflur, it is also used in the form of gels for the treatment of early stages of caries, sensitive teeth, and by dentists for the refluoridation of damaged tooth enamel. Olaflur is a salt consisting of an alkyl ammonium cation and fluoride as the counterion. With a long lipophilic hydrocarbon chain, the cation has surfactant properties. It forms a film layer on the surface of teeth, which facilitates incorporation of fluoride into the enamel. The top layers of the enamel's primary mineral, hydroxylapatite, are converted into the more robust fluorapatite. The fluoridation reaches only a depth of a few nanometres, which has raised doubts whether the mechanism really relies on the formation of fluorapatite.

CNS Activity

Originator

Sources: Helvetica Odontologica Acta (1962), 6, (1), 15-20.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
elmex

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Allergic contact cheilitis caused by olaflur in toothpaste.
2017-01
Cytotoxicity of organic surface coating agents used for nanoparticles synthesis and stability.
2015-06
Oleylamine as a beneficial agent for the synthesis of CoFe₂O₄ nanoparticles with potential biomedical uses.
2014-05-07
Sensitivity of human dental pulp cells to eighteen chemical agents used for endodontic treatments in dentistry.
2013-01
Successful extracorporeal life support after potentially fatal pulmonary oedema caused by inhalation of nitric and hydrofluoric acid fumes.
2007-10
Epidemiology of 377 patients with chemical burns in Guangdong province.
2004-09
An improved method for emergent decontamination of ocular and dermal hydrofluoric acid splashes.
2004-08
Patents

Patents

Sample Use Guides

toxicity in mice: LD50 = 888 mg/kg
Route of Administration: Intraperitoneal
Cytotoxicity study: it was explored the cytotoxicity of the coating agent, Oleylamine in two cell lines, human epidermal keratinocyte (HaCaT) and lung fibroblast (CRL-1490) cells, at surface coating agent concentrations of 3, 10, 30, and 100 μM. Two exposure time points, 2 h, and 24 h were employed for the study. Oleylamine, is highly toxic, leading to almost 100% cell death.
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:59:39 GMT 2025
Edited
by admin
on Mon Mar 31 17:59:39 GMT 2025
Record UNII
3FTR44B32Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
STANNOUS FLUORIDE [HSDB]
Preferred Name English
STANNOUS FLUORIDE
HSDB   II   INCI   MART.   MI   USP   VANDF   WHO-DD  
INCI  
Official Name English
Tin fluoride (SnF2)
Common Name English
STANNOUS FLUORIDE [MI]
Common Name English
STANNOUS FLUORIDE [VANDF]
Common Name English
STANNOUS FLUORIDE [II]
Common Name English
STANNOUS FLUORIDE [MART.]
Common Name English
Stannous fluoride [WHO-DD]
Common Name English
STANNOUS FLUORIDE [USP MONOGRAPH]
Common Name English
Classification Tree Code System Code
WHO-ATC A01AA04
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
CFR 21 CFR 355.60
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
CFR 21 CFR 355.55
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
CFR 21 CFR 355.50
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
CFR 21 CFR 355.10
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
CFR 21 CFR 355.70
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
NCI_THESAURUS C28394
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
WHO-VATC QA01AA04
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
CFR 21 CFR 355.20
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
Code System Code Type Description
HSDB
783
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
PRIMARY
EVMPD
SUB15374MIG
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
PRIMARY
NCI_THESAURUS
C77058
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
PRIMARY
PUBCHEM
134688170
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
PRIMARY
DAILYMED
3FTR44B32Q
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
PRIMARY
RXCUI
10030
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
PRIMARY RxNorm
DRUG BANK
DB11092
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
PRIMARY
EPA CompTox
DTXSID6064822
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PRIMARY
DRUG CENTRAL
4273
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
PRIMARY
ECHA (EC/EINECS)
231-999-3
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
PRIMARY
CAS
7783-47-3
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PRIMARY
MERCK INDEX
m10181
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
PRIMARY Merck Index
FDA UNII
3FTR44B32Q
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
PRIMARY
WIKIPEDIA
Tin(II) fluoride
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
PRIMARY
SMS_ID
100000077812
Created by admin on Mon Mar 31 17:59:39 GMT 2025 , Edited by admin on Mon Mar 31 17:59:39 GMT 2025
PRIMARY
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ACTIVE MOIETY