ChemicalBook > CAS DataBase List > Phenyl salicylate

Phenyl salicylate

Product Name
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
Formula Weight
214.22
MOL File
118-55-8.mol
More
Less

Phenyl salicylate Property

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
form 
Fine Crystalline Powder
pka
8.71±0.10(Predicted)
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
CAS DataBase Reference
118-55-8(CAS DataBase Reference)
NIST Chemistry Reference
Benzoic acid, 2-hydroxy-, phenyl ester(118-55-8)
EPA Substance Registry System
Phenyl salicylate (118-55-8)
More
Less

Safety

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
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H317May cause an allergic skin reaction

H319Causes serious eye irritation

H411Toxic to aquatic life with long lasting effects

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
149187
Product name
Phenyl salicylate
Purity
ReagentPlus , 99%
Packaging
250g
Price
$67.5
Updated
2024/03/01
Sigma-Aldrich
Product number
149187
Product name
Phenyl salicylate
Purity
ReagentPlus , 99%
Packaging
50g
Price
$57.8
Updated
2023/06/20
TCI Chemical
Product number
S0017
Product name
Phenyl Salicylate
Purity
>98.0%(GC)
Packaging
25g
Price
$26
Updated
2024/03/01
TCI Chemical
Product number
S0017
Product name
Phenyl Salicylate
Purity
>98.0%(GC)
Packaging
500g
Price
$95
Updated
2024/03/01
Alfa Aesar
Product number
B20686
Product name
Phenyl salicylate, 99%
Packaging
100g
Price
$31.7
Updated
2024/03/01
More
Less

Phenyl salicylate Chemical Properties,Usage,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

Preparation Products

More
Less

Phenyl salicylate Suppliers

Yueyang Chenran Pharmaceutical Technology Co., Ltd
Tel
15973029516
Email
46804146@qq.com
Country
China
ProdList
16
Advantage
58
Jinan Londi Medical Technology Co., LTD
Tel
0531-88996911 15628983711
Fax
0531-88996911
Email
3305202763@qq.com
Country
China
ProdList
125
Advantage
58
Wuhan Fortuna Chemical Co., Ltd
Tel
027-59207852 13308628970
Fax
QQ:2779667926
Email
buy@fortunachem.com
Country
China
ProdList
2793
Advantage
58
Suzhou Yuanrui Bio-Tech Co., Ltd
Tel
18106132862 18106132862
Email
sales02@yuanruibio.com
Country
China
ProdList
222
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94657
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Beijing HwrkChemical Technology Co., Ltd
Tel
010-89508211 18501085097
Fax
010-89508210
Email
sales.bj@hwrkchemical.com
Country
China
ProdList
8418
Advantage
55
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44689
Advantage
61
More
Less

View Lastest Price from Phenyl salicylate manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Phenyl salicylate 118-55-8
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50tons/month
Release date
2021-07-22
Hebei Weibang Biotechnology Co., Ltd
Product
Phenyl salicylate 118-55-8
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-11-21
Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
Phenyl salicylate 118-55-8
Price
US $10.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20ton
Release date
2024-05-22

118-55-8, Phenyl salicylateRelated Search:


  • Phenyl 2-hydroxybenzoate(Phenyl salicylate)
  • Phenyl salicy
  • Phenyl salicylate,Salol
  • Phenyl Salicylate, crystal
  • Phenyl Salicylate Melting Point Standard (500 mg) (Approximately 41 degrees)
  • Phenyl salicylate, 99% 250GR
  • 2-Hydroxybenzoic Acid Phenyl Ester Phenyl 2-Hydroxybenzoate Salicylic Acid Phenyl Ester
  • Salicylic acid phenyl
  • Phenyl salicylate, 2-(Phenoxycarbonyl)phenol, Salol
  • Phenyl Salicytate
  • Phenyl salicylate melting point standard
  • Mettler-Toledo Calibration substance ME 30034252, Phenyl salicylate
  • Phenyl salicylate ReagentPlus(R), 99%
  • Phenyl salicylate Vetec(TM) reagent grade, 98%
  • Salol 2-Hydroxybenzoic Acid Phenyl Ester Phenyl 2-Hydroxybenzoate Salicylic Acid Phenyl Ester
  • Phenyl salicylate 118-55-8
  • Salicylic Acid Phenyl Ester Phenyl salicylate
  • 2-HYDROXYBENZOIC ACID PHENYL ESTER
  • 'LGC' (2411)
  • 'LGC' (2613)
  • LABOTEST-BB LT00053052
  • Disperse Dye Blue EXSF
  • FEMA 3960
  • AURORA KA-3673
  • Phenyl Salicylate/Phenyl 2-hydroxybenzoate/Salol
  • SALOL
  • SALICYLIC ACID PHENYL ESTER
  • PHENYL 2-HYDROXYBENZOATE
  • PHENYL SALICYLATE
  • PHENYL-O-HYDROXYBENZOATE
  • O-HYDROXYBENZOIC ACID PHENYL ESTER
  • PHENYL SALICYLATE 99+%
  • Phenyl2-hydroxybenzoate=Salol
  • PHENYLSALICYLATE,CRYSTAL,PURIFIED
  • Phenylsalicylat
  • Benzoicacid,2-hydroxy-,phenylester
  • Fenylester kyseliny salicylove
  • fenylesterkyselinysalicylove
  • Musol
  • Phenol salicylate
  • Salphenyl
  • Seesorb 201
  • Seesorb K 201
  • 2-hydroxy-benzoicaciphenylester
  • 2-Phenoxycarbonylphenol
  • Phenyl salicylate CAS:118-55-8
  • Phenyl Salicylate &gt
  • Phenyl salicylate USP/EP/BP
  • Phenyl Salicylate (Salol) extrapure, 99%
  • Phenyl Salicylate, Extra Pure, SLR, Fisher Chemical
  • NSC 33406
  • NSC33406
  • NSC-33406
  • Phenyl Salicylate, ≥ 98.0%
  • Phenyl 2-hydroxybenzoate in methanol
  • 118-55-8
  • 204-259-2
  • 2HOC6H4CO2C6H5