ChemicalBook > CAS DataBase List > 2-HYDROXY-4-METHOXY-4'-METHYLBENZOPHENONE

2-HYDROXY-4-METHOXY-4'-METHYLBENZOPHENONE

Product Name
2-HYDROXY-4-METHOXY-4'-METHYLBENZOPHENONE
CAS No.
1641-17-4
Chemical Name
2-HYDROXY-4-METHOXY-4'-METHYLBENZOPHENONE
Synonyms
Uvistat;MEXENONE;Mesenone;MEXENEONE;Uvistat L;''MEXENONE'';BENZOPHENONE-10;Mesenone [DCIT];LABOTEST-BB LT00455260;inhibit,Mexenone,Inhibitor
CBNumber
CB8188500
Molecular Formula
C15H14O3
Formula Weight
242.27
MOL File
1641-17-4.mol
More
Less

2-HYDROXY-4-METHOXY-4'-METHYLBENZOPHENONE Property

Melting point:
99-102°C
Boiling point:
345.09°C (rough estimate)
Density 
1.1515 (rough estimate)
refractive index 
1.5570 (estimate)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform (Slightly, Heated), Methanol (Slightly, Heated)
pka
7.35±0.35(Predicted)
form 
Solid
color 
Pale Yellow to Light Yellow
Merck 
14,6167
BRN 
1972646
LogP
4.100 (est)
CAS DataBase Reference
1641-17-4(CAS DataBase Reference)
More
Less

Safety

Risk Statements 
36/37/38
Safety Statements 
26-36
Hazardous Substances Data
1641-17-4(Hazardous Substances Data)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H317May cause an allergic skin reaction

H319Causes serious eye irritation

Precautionary statements

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

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P272Contaminated work clothing should not be allowed out of the workplace.

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.

P333+P313IF SKIN irritation or rash occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
S408883
Product name
2-HYDROXY-4-METHOXY-4'-METHYLBENZOPHENONE
Purity
Aldrich
Packaging
1g
Price
$179
Updated
2024/03/01
TRC
Product number
H939938
Product name
(2-Hydroxy-4-methoxyphenyl)(4-methylphenyl)methanone
Packaging
100mg
Price
$70
Updated
2021/12/16
Matrix Scientific
Product number
157387
Product name
(2-Hydroxy-4-methoxyphenyl)(4-methylphenyl)methanone
Packaging
0.500g
Price
$120
Updated
2021/12/16
Matrix Scientific
Product number
157387
Product name
(2-Hydroxy-4-methoxyphenyl)(4-methylphenyl)methanone
Packaging
1g
Price
$150
Updated
2021/12/16
Matrix Scientific
Product number
157387
Product name
(2-Hydroxy-4-methoxyphenyl)(4-methylphenyl)methanone
Packaging
5g
Price
$460
Updated
2021/12/16
More
Less

2-HYDROXY-4-METHOXY-4'-METHYLBENZOPHENONE Chemical Properties,Usage,Production

Originator

Uvistat-L,Ward Blenkinsop,UK,1960

Uses

2-Hydroxy-4-methoxy-4'-methyl-benzophenone is an UV absorbing agent in sunscreen cosmetic creams, lotions, lipstieks, sun oils, etc.

Preparation

Preparation by Friedel–Crafts acylation of m-methoxy-phenol with p-toluoyl chloride,
in the presence of boron trichloride in benzene first at ?10°, then at reflux for 10 h under nitrogen (80%)
in the presence of titanium tetrachloride in benzene first at ?10°, then at reflux for 14 h under nitrogen (73%) or in chlorobenzene for 1 h at 120° (79%).

Definition

ChEBI: Mexenone is a member of benzophenones.

Manufacturing Process

p-Toluoyl chloride is the starting material. To this is added chlorobenzene and 1,3-dimethoxybenzene. The reaction mixture is cooled to 12°C in an ice bath and aluminum chloride is added gradually, keeping the reaction below 30°C. The reaction is then gradually heated to 115°C with the evolution of hydrogen chloride gas. As the temperature increases, the reaction mixture becomes thicker. At 105°C, dimethyl formamide is added slowly. The reaction is heated at 115°C for a short time and is then poured into concentrated hydrochloric acid. The reaction mixture pours very easily and very cleanly. The acid mixture is heated with steam to dissolve all the material which had not hydrolyzed and the mixture is filtered. The red chlorobenzene layer is separated and washed twice with hot water.
To the chlorobenzene solution is then added sodium hydroxide dissolved in water and the chlorobenzene is removed by a steam distillation. After all of the chlorobenzene is removed, the precipitate which forms during the distillation is removed by filtration and discarded. The solution is cooled and acidified with hydrochloric acid, precipitating a tan solid. This is removed by filtration and washed acid-free. It is then treated with sodium bicarbonate solution to remove any acid present and is then washed with water to remove all traces of bicarbonate. After drying approximately a 75% yield of mexenone is obtained.

Therapeutic Function

Sunscreen agent

Contact allergens

BZP-10 is exceptionally positive in ketoprofen-photosensitive patients.

2-HYDROXY-4-METHOXY-4'-METHYLBENZOPHENONE Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

2-HYDROXY-4-METHOXY-4'-METHYLBENZOPHENONE Suppliers

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
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
chenyj@titansci.com
Country
China
ProdList
14103
Advantage
59
Beckmann-Kenko GmbH
Tel
+49 4241 9308 88
Fax
+49 4241 9308 89
Email
info@beckmann-kenko.com
Country
Germany
ProdList
478
Advantage
62
UHN Shanghai Research & Development Co., Ltd.
Tel
021-58958002 18930822973
Fax
+86 (21) 5895-8628
Email
SALES@UHNSHANGHAI.COM
Country
China
ProdList
977
Advantage
58
Shanghai Raise Chemical Technology Co.,Ltd
Tel
15026594951
Fax
0556-5030632
Email
rs@raise-chem.com
Country
China
ProdList
3576
Advantage
55
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
27313
Advantage
60
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131957
Advantage
58
Guangdong wengjiang Chemical Reagent Co., Ltd.
Tel
0751-2886750 13927877953
Fax
0751-2886750
Email
3005811397@qq.com
Country
China
ProdList
13320
Advantage
58
Shandong Ono Chemical Co., Ltd.
Tel
0539-6362799 20)
Fax
0539-6362799(To 20)
Country
China
ProdList
9998
Advantage
58

1641-17-4, 2-HYDROXY-4-METHOXY-4'-METHYLBENZOPHENONERelated Search:


  • 2-HYDROXY-4-METHOXY-4'-METHYLBENZOPHENONE
  • LABOTEST-BB LT00455260
  • MEXENONE
  • ''MEXENONE''
  • BENZOPHENONE-10
  • benzophenone-10,2-hydroxy-4-methoxy-4’-methylbenzophenone
  • HYDROXYMETHOXYMETHYLBENZOPHENONE
  • 2-HYDROXY-METHOXYMETHYLBENZOPHENONE
  • (2-Hydroxy-4-methoxyphenyl)(4-methylphenyl)methanone
  • 2-HYDROXY-4-METHOXY-4''-METHYLBENZOPHENONE, 98+%
  • (2-Hydroxy-4-methoxyphenyl)(4-methylphenyl) ketone
  • Uvistat
  • (2-Hydroxy-4-Methoxyphenyl)(p-tolyl)Methanone
  • MEXENEONE
  • Mesenone [DCIT]
  • Methanone, (2-hydroxy-4-methoxyphenyl)(4-methylphenyl)-
  • Uvistat L
  • Mesenone
  • inhibit,Mexenone,Inhibitor
  • 2-HYDROXY-4-METHOXY-4'-METHYLBENZOPHENONE
  • 2-Hydroxy-4-methoxy-4-mrthylbenzophenone in methanol
  • 1641-17-4
  • 164-17-4
  • Aromatic Benzophenones & Derivatives (substituted)
  • UVISTAT