Phenyl salicylate
- CAS No.
- 118-55-8
- Chemical Name:
- Phenyl salicylate
- Synonyms
- SALOL;FEMA 3960;Salphenyl;PHENYL 2-HYDROXYBENZOATE;Musol;NSC33406;NSC 33406;NSC-33406;Seesorb 201;'LGC' (2411)
- CBNumber:
- CB9322550
- Molecular Formula:
- C13H10O3
- Molecular Weight:
- 214.22
- MDL Number:
- MFCD00002213
- MOL File:
- 118-55-8.mol
- MSDS File:
- SDS
Melting point | 41-43 °C (lit.) |
---|---|
Boiling point | 172-173 °C/12 mmHg (lit.) |
Density | 1.250g/cm3 |
refractive index | 1.5090 (estimate) |
FEMA | 3960 | PHENYL SALICYLATE |
Flash point | >230 °F |
storage temp. | 2-8°C |
solubility | dioxane: 0.1 g/mL, clear, colorless |
pka | 8.71±0.10(Predicted) |
form | Fine Crystalline Powder |
color | White |
Odor | at 100.00 %. mild sweet fruity balsam |
Odor Type | balsamic |
Water Solubility | Soluble in alcohol, ether, chloroform, turpentine, acetone and benzene. Sparingly soluble in chloroformbenzene. Insoluble in water. |
Merck | 14,7310 |
JECFA Number | 736 |
BRN | 393969 |
Dielectric constant | 6.3(50.0℃) |
Stability | Light sensitive. Incompatible with strong oxidants. Flammable. |
LogP | 3.55 |
Substances Added to Food (formerly EAFUS) | PHENYL SALICYLATE |
FDA 21 CFR | 177.1010; 310.545 |
CAS DataBase Reference | 118-55-8(CAS DataBase Reference) |
EWG's Food Scores | 1-3 |
FDA UNII | 28A37T47QO |
ATC code | G04BX12 |
NIST Chemistry Reference | Benzoic acid, 2-hydroxy-, phenyl ester(118-55-8) |
EPA Substance Registry System | Phenyl salicylate (118-55-8) |
SAFETY
Risk and Safety Statements
Symbol(GHS) | ![]() ![]() GHS07,GHS09 |
|||||||||
---|---|---|---|---|---|---|---|---|---|---|
Signal word | Warning | |||||||||
Hazard statements | H315-H317-H319-H411 | |||||||||
Precautionary statements | P261-P264-P273-P280-P302+P352-P305+P351+P338 | |||||||||
Hazard Codes | Xi | |||||||||
Risk Statements | 36/37/38 | |||||||||
Safety Statements | 26-36-24/25 | |||||||||
RIDADR | UN 3077 9 / PGIII | |||||||||
WGK Germany | 2 | |||||||||
RTECS | VO6125000 | |||||||||
TSCA | Yes | |||||||||
HS Code | 29182300 | |||||||||
NFPA 704 |
|
Phenyl salicylate price More Price(30)
Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
---|---|---|---|---|---|---|---|
Sigma-Aldrich | 149187 | Phenyl salicylate ReagentPlus , 99% | 118-55-8 | 250g | $67.5 | 2024-03-01 | Buy |
Sigma-Aldrich | 149187 | Phenyl salicylate ReagentPlus , 99% | 118-55-8 | 50g | $57.8 | 2023-06-20 | Buy |
TCI Chemical | S0017 | Phenyl Salicylate >98.0%(GC) | 118-55-8 | 25g | $26 | 2024-03-01 | Buy |
TCI Chemical | S0017 | Phenyl Salicylate >98.0%(GC) | 118-55-8 | 500g | $95 | 2024-03-01 | Buy |
Alfa Aesar | B20686 | Phenyl salicylate, 99% | 118-55-8 | 100g | $31.7 | 2024-03-01 | Buy |
Phenyl salicylate Chemical Properties,Uses,Production
Description
Phenyl salicylate, also referred to as salol, is a member of the hydroxybenzoic acid family of organic compounds. Its chemical formula is C13H10O3. It is manufactured through the chemical reaction between phenol and salicylic acid. Phenyl salicylate is a good antiseptic that is used in the production of toothpaste. It has several medical properties, including its ability to act as an analgesic, anti-septic with antibacterial properties, and antipyretic to reduce fever. Additionally, it can be utilized for treating lower urinary tract inflammation. Although it is no longer widely used in human medicine, it is still employed in veterinary medicine.
Chemical Properties
Phenyl salicylate is a white crystalline solid that has a balsamic type odor. It readily dissolves in ether, benzene, and chloroform, and can be dissolved in ethanol, but is almost insoluble in water and glycerol.
Uses
Phenyl salicylate is used as an analgesic and antipyretic. It is also used in the manufacture of polymer plastics, lacquers, waxes, polishes, adhesives, and sunscreen products(suntan oils and cremes). As light absorber to prevent discoloration of plastics. It is also a fragrance ingredient, but has limited use. in veterinary use as an external disinfectant and intestinal antiseptic agent.
Preparation
Phenyl salicylate was synthesized by esterification of salicylic acid and phenol in the presence of catalyst sulfuric acid. The esterification liquid is neutralized, washed with water and distilled to obtain the finished product. It also can preparation by the action of phosphorus oxychloride on a mixture of phenol and salicylic acid (Merck Index, 1968).
Definition
ChEBI: Phenyl salicylate is a benzoate ester that is the phenyl ester of salicylic acid. Also known as salol, it can be formed by heating salicylic acid with phenol and is used in the manufacture of some polymers, lacquers, adhesives, waxes and polishes. It has a role as an ultraviolet filter. It is a benzoate ester, a member of phenols and a member of salicylates. It derives from a salicylic acid.
Taste threshold values
Sweet, mildly medicinal taste at concentrations near 50 ppm.
Toxicity evaluation
The acute oral LD50 value in rats was reported as 3 g/kg and the acute dermal LD50 value in rabbits exceeded 5 g/kg (Levenstein, 1975). The probable LD in man is 50-500 mg/kg. The toxic effects of phenyl salicylate are similar to those of phenol but do not include a corrosive action on the alimentary canal (Dittmer, 1959).
General Description
Phenyl salicylate is a phenyl ester of salicylic acid and is used as a medicine under the name ′salol′ as an internal antiseptic. It finds its application in paints, waxes, and varnishes as it is found to absorb UV radiation in the range of 290-325 nm. It also shows its presence in cosmetics and sunscreens as a UV filter.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
Incompatible with bromine water, ferric salts, camphor, phenol, chloral hydrate, monobrominated camphor, thymol, or urethane in trituration. .
Fire Hazard
Flash point data for Phenyl salicylate are not available, however Phenyl salicylate is probably combustible.
Pharmacology
Phenyl salicylate was found to have slight analgesic activity against pain stimuli in mice (Kameyama, 1961), but ip administration of 500 mg/kg showed no analgesic action against an electric shock applied to the tails of mice (McKenzie & Beechey, 1962). In vitro studies on cartilage and rat-liver mitochondria have shown that phenyl salicylates are more active than salicylates in uncoupling oxidative phosphorylation (Bostrom, Berntsen & Whitehouse, 1964).
Safety Profile
Moderately toxic by ingestion. Experimental teratogenic and reproductive effects. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS
Metabolism
According to Baas (1890) from 44 to 96% of a dose (5-8 g) of phenyl salicylate is hydrolysed in man and none of it is found in the faeces. An increase in the ethereal sulphates of the urine after its ingestion is due, no doubt, to the phenol liberated (Williams, 1959). Phenyl salicylate is hydrolysed in the gut primarily to phenol and salicylic acid, which are rapidly absorbed and excreted (Fassett, 1963), but it was not hydrolysed by a partially purified preparation of acetylarylesterase from human plasma (Augustinsson & Ekedahl, 1962). Intestinal absorption and excretion of orally administered phenyl salicylate were studied in rabbits and dogs by analysis of blood and urine samples; oral administration of glucosamine hydrochloride increased the blood concentration of phenyl salicylate but had little effect on urinary excretion (Tanaka, Kojima & Matsubara, 1961).
Purification Methods
Fractionally crystallise salol from its melt, then crystallise it from *benzene. [Beilstein 10 IV 154.]
References
https://pubchem.ncbi.nlm.nih.gov/compound/Phenyl_salicylate
http://www.wisegeek.com/what-are-the-medical-uses-of-phenyl-salicylate.htm
https://en.wikipedia.org/wiki/Phenyl_salicylate
https://www.sigmaaldrich.com/SG/en/product/sial/phr1152
Phenyl salicylate Preparation Products And Raw materials
Raw materials
1of2
Preparation Products
1of2
Supplier | Tel | Country | ProdList | Advantage | |
---|---|---|---|---|---|
Suzhou Yuanrui Bio-Tech Co., Ltd | +86-18106132862 +86-18106132862 | sales02@yuanruibio.com | China | 285 | 58 |
Hebei Mojin Biotechnology Co., Ltd | +8613288715578 | sales@hbmojin.com | China | 12450 | 58 |
Hebei Yanxi Chemical Co., Ltd. | +86-17531190177; +8617531190177 | peter@yan-xi.com | China | 5873 | 58 |
Hebei Guanlang Biotechnology Co,.LTD | +8619930503252 | daisy@crovellbio.com | China | 5828 | 58 |
Wuhan Han Sheng New Material Technology Co.,Ltd | +8617798174412 | admin01@hsnm.com.cn | China | 2118 | 58 |
Shandong Juchuang Chemical Co., LTD | +undefined15030412209 | admin@juchuangchem.com | China | 387 | 58 |
Hebei Zhuanglai Chemical Trading Co.,Ltd | +8613343047651 | admin@zlchemi.com | China | 3002 | 58 |
Hebei Mojin Biotechnology Co.,Ltd | +8613288715578 | angelia@hbmojin.com | China | 830 | 58 |
Shanghai Daken Advanced Materials Co.,Ltd | +86-371-66670886 | info@dakenam.com | China | 16914 | 58 |
Henan Tianfu Chemical Co.,Ltd. | +86-0371-55170693 +86-19937530512 | info@tianfuchem.com | China | 21668 | 55 |
View Lastest Price from Phenyl salicylate manufacturers
Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
---|---|---|---|---|---|---|---|---|
![]() |
2024-08-22 | Phenyl salicylate
118-55-8
|
US $2.00-2.00 / KG | 10KG | 99% | 10000kg | Hebei Guanlang Biotechnology Co,.LTD | |
![]() |
2024-08-22 | Phenyl salicylate
118-55-8
|
US $0.00 / KG | 1KG | 99% | 50tons/month | WUHAN FORTUNA CHEMICAL CO., LTD | |
![]() |
2024-08-21 | Phenyl salicylate
118-55-8
|
US $0.00 / kg | 1kg | 99% | 50000KG/month | Hebei Mojin Biotechnology Co.,Ltd |
-
- Phenyl salicylate
118-55-8
- US $2.00-2.00 / KG
- 99%
- Hebei Guanlang Biotechnology Co,.LTD
-
- Phenyl salicylate
118-55-8
- US $0.00 / KG
- 99%
- WUHAN FORTUNA CHEMICAL CO., LTD
-
- Phenyl salicylate
118-55-8
- US $0.00 / kg
- 99%
- Hebei Mojin Biotechnology Co.,Ltd