Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H7O2.Na |
Molecular Weight | 134.1083 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 2 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].C\C=C\C=C\C([O-])=O
InChI
InChIKey=LROWVYNUWKVTCU-STWYSWDKSA-M
InChI=1S/C6H8O2.Na/c1-2-3-4-5-6(7)8;/h2-5H,1H3,(H,7,8);/q;+1/p-1/b3-2+,5-4+;
Molecular Formula | Na |
Molecular Weight | 22.9898 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C6H7O2 |
Molecular Weight | 111.1186 |
Charge | -1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 2 |
Optical Activity | NONE |
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/2253815Curator's Comment: description was created based on several sources, including
https://www.extension.iastate.edu/wine/sites/www.extension.iastate.edu/files/wine/SorbicAcid1.pdf
Sources: http://www.ncbi.nlm.nih.gov/pubmed/2253815
Curator's Comment: description was created based on several sources, including
https://www.extension.iastate.edu/wine/sites/www.extension.iastate.edu/files/wine/SorbicAcid1.pdf
A. W. Van Hoffman was the first to isolate sorbic acid from the berries of the mountain ash tree in the year 1859. The antimicrobial (preservative) properties of sorbic acid were recognized in the 1940's. In the late 1940's and 1950's it became commercially available. Sorbic acid and its potassium salt are now used in many countries in the production of sweet white wines. In the United States, BATF permits the use of sorbic acid and potassium sorbate to preserve wine. The maximum concentration of sorbic acid allowed in finished wine is 300 mg/L, (300 ppm). The antimicrobial action of sorbic acid is primarily against yeasts and molds. It's action against bacteria appears to be selective. The soluble sorbates are preferred when it is desired to use the preservative in liquid form, or when aqueous systems are to be preserved. Sodium sorbate in solid form is unstable and very rapidly undergoes oxidation on exposure to atmospheric oxygen. It is therefore not produced on the industrial scale. Aqueous solutions of sodium sorbate remain stable for some time. Calcium sorbate is used in the manufacture of fungistatic wrappers because it is highly stable to oxidation, but this use is very limited. Sorbic acid and sorbates can be directly added into the product. The products can be dipped or sprayed with aqueous solutions of sorbates. Dusting of food with dry sorbic acid is also possible but less recommended because sorbic acid irritates the skin and mucous membranes. Sorbic acid and particularly calcium sorbate can be used as active substances in fungistatic wrappers. A general survey of the numerous uses of sorbic acid in the food sector will be given. Some fields of application will be discussed that are either unimportant or not permitted in the U.K.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: mold catalase Sources: http://www.ncbi.nlm.nih.gov/pubmed/5861281 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Inactive ingredient | 24 HOUR PIMPLE PUNISHER Approved UseFor treatment of Acne. Helps keep skin clear of new acne blemishes. |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 01:28:30 GMT 2023
by
admin
on
Sat Dec 16 01:28:30 GMT 2023
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Record UNII |
TGW6Q2CCVM
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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CODEX ALIMENTARIUS (GSFA) |
INS-201
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JECFA EVALUATION |
INS-201
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Code System | Code | Type | Description | ||
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DTXSID8047181
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23665582
Created by
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SODIUM SORBATE
Created by
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TGW6Q2CCVM
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7757-81-5
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m10117
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PRIMARY | Merck Index | ||
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231-819-3
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771
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |