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.

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
1
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 Yuqing Jiaheng Pharmaceutical Co., Ltd.
Tel
027-83850122 13343472658
Email
918571372@qq.com
Country
China
ProdList
1809
Advantage
58
Baynoe Chem (Suzhou) Co., Ltd.
Tel
18934593683
Email
sales06@baynoe.com
Country
China
ProdList
708
Advantage
58
Wuhan Fortuna Chemical Co., Ltd
Tel
027-027-59207852 13308628970
Fax
QQ:2779667926
Email
buy@fortunachem.com
Country
China
ProdList
2640
Advantage
58
Suzhou Yuanrui Bio-Tech Co., Ltd
Tel
18106132862 18106132862
Email
sales02@yuanruibio.com
Country
China
ProdList
146
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40241
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30132
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18501085097
Fax
010-89508210
Email
sales3.gd@hwrkchemical.com
Country
China
ProdList
7583
Advantage
55
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44751
Advantage
61
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
zhangsn@titansci.com
Country
China
ProdList
14113
Advantage
59
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696;
Email
info@hanhongsci.com
Country
China
ProdList
42982
Advantage
64
Shandong Xiya Chemical Co., Ltd
Tel
13355009207 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18739
Advantage
57
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12990
Advantage
57
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14443
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9823
Advantage
79
Shanghai Sunway Pharmaceutical Technology Co., Ltd
Tel
+8618575662672 18575662672
Fax
021 51613951
Email
mzeng@3wpharm.com
Country
China
ProdList
9756
Advantage
57
Maya High Purity Chemicals
Tel
+86 (573) 82222445 (0)18006601000 452520369
Fax
+86 (573) 82222643
Email
sales@maya-r.com
Country
China
ProdList
11714
Advantage
57
ZhengZhou HuaWen Chemical Co.Ltd
Tel
0370-2785118 15343847665
Fax
QQ:3470079902
Email
huawenchem@163.com
Country
China
ProdList
3206
Advantage
55
Spectrum Chemical Manufacturing Corp.
Tel
021-021-021-67601398-809-809-809 15221380277
Fax
021-57711696
Email
marketing_china@spectrumchemical.com
Country
China
ProdList
9664
Advantage
60
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9725
Advantage
55
Shanghai civi chemical technology co.,Ltd
Tel
86-21-34053660
Fax
86-21-34053661
Email
sale@labgogo.com
Country
China
ProdList
9872
Advantage
52
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17779
Advantage
75
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12338
Advantage
58
Beijing innoChem Science & Technology Co.,Ltd.
Tel
400-810-7969 010-59572699
Fax
010-59572688
Email
ningzi.li@inno-chem.com.cn
Country
China
ProdList
6139
Advantage
55
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611
Fax
+86 21 50676805
Country
China
ProdList
9901
Advantage
58
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22519
Advantage
55
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-6206333 18521732826;
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25004
Advantage
65
The future of Shanghai Industrial Co., Ltd.
Tel
021-61552785
Fax
021-55660885
Email
sales@shshiji.com
Country
China
ProdList
9552
Advantage
55
TargetMol Chemicals Inc.
Tel
021-33632979 15002134094
Fax
021-33632979
Email
marketing@targetmol.com
Country
China
ProdList
7934
Advantage
58
Quzhou Juhua Friendship Co., Ltd
Tel
0570-3066667
Fax
0570-3063388
Country
China
ProdList
3933
Advantage
58
Beijing Universal Century Technology Co., Ltd.
Tel
400-8706899
Fax
400-8706899
Email
hysj_bj.com
Country
China
ProdList
3585
Advantage
55
Shanghai JONLN Reagent Co., Ltd.
Tel
400-0066400 13621662912
Fax
021-55660885
Email
422131432@qq.com
Country
China
ProdList
9986
Advantage
55
TianJin Alta Scientific Co., Ltd.
Tel
022-65378550-8551
Fax
+86-022-2532-9655
Email
contact@altascientific.com
Country
China
ProdList
2773
Advantage
58
Bide Pharmatech Ltd.
Tel
400-1647117 15221909166
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
41132
Advantage
60
RiZhao LiDeShi Chemical Co., Ltd.
Tel
010-51268198
Fax
010-63833209
Email
leadershipchem@126.com
Country
China
ProdList
2549
Advantage
58
Mei Lan Industrial (Shanghai) Co., Ltd.
Tel
021-58958189
Fax
021-58957967
Email
wouchina@126.com
Country
China
ProdList
2671
Advantage
55
ChemStrong Scientific Co.,Ltd
Tel
0755-66853366 13670046396
Fax
0755-28363542
Email
sales@chem-strong.com
Country
China
ProdList
17982
Advantage
56
Shanghai ideal Industrial Co., Ltd.
Tel
021-58957966 18930537195
Fax
021-60899437
Email
wouchina@126.com
Country
China
ProdList
3033
Advantage
58
HUBEI RISON CHEMICAL CO.,LTD
Tel
027 83642615 13995607107
Fax
027 83660699
Email
market@risonchem.com
Country
China
ProdList
280
Advantage
58
Chengdu HuaXia Chemical Reagent Co. Ltd
Tel
400-1166-196 13458535857
Fax
QQ:800101999
Email
cdhxsj@163.com
Country
China
ProdList
13358
Advantage
58
GuangTuo Chemical (Shanghai) Co., Ltd.
Tel
021-60899189-8001 18918189673
Fax
021-60899304
Email
gtchem@126.com
Country
China
ProdList
2661
Advantage
58
Shanghai yongzeng technology co., LTD
Tel
021-021-65281118 15921781258
Fax
021-6528 2963
Email
sales@yongzchem.com
Country
China
ProdList
64
Advantage
58
Wuhan Dahua Pharmaceutical Co., Ltd.
Tel
027-59262863 13277907145 3091977954
Fax
027-59420980
Country
China
ProdList
4951
Advantage
58
Shanghai YuLue Chemical Co., Ltd.
Tel
021-60345187 13671753212
Fax
021-34702061
Email
lzz841106@aliyun.com
Country
China
ProdList
10287
Advantage
55
Shanghai Macklin Biochemical Co.,Ltd.
Tel
15221275939 15221275939
Fax
021-50706099
Email
shenlinxing@macklin.cn
Country
China
ProdList
15878
Advantage
55
Hangzhou J&H Chemical Co., Ltd.
Tel
+86-571-87396432 0571-87396433
Fax
0571-87396431
Email
sales@jhechem.com
Country
China
ProdList
10015
Advantage
53
Wuhan Dahua Weiye Pharmaceutical Chemical Co., Ltd.
Tel
027-59420981,18702770802
Fax
027-83322098
Country
China
ProdList
1975
Advantage
50
More
Less

View Lastest Price from Phenyl salicylate manufacturers

Shandong Juchuang Chemical Co., LTD
Product
Salicylic Acid Phenyl 118-55-8
Price
US $38.00-22.00/kg
Min. Order
500kg
Purity
99.9
Supply Ability
200tons
Release date
2024-03-13
Hebei Yanxi Chemical Co., Ltd.
Product
Phenyl salicylate 118-55-8
Price
US $40.00-40.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
10 tons
Release date
2023-09-12
Suzhou Yuanrui Bio-Tech Co., Ltd
Product
Phenyl salicylate 118-55-8
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
50tons
Release date
2023-11-19

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%
  • 118-55-8
  • 204-259-2
  • 2HOC6H4CO2C6H5
  • C6H4OHCOOC6H5