Uses
ChemicalBook > CAS DataBase List > Menbutone

Menbutone

Uses
Product Name
Menbutone
CAS No.
3562-99-0
Chemical Name
Menbutone
Synonyms
menbutone;genabil;menbuton;fel-bis;Icteryl;SC 1749;naftobil;genabilin;epanaftol;Meng Meng
CBNumber
CB3489226
Molecular Formula
C15H14O4
Formula Weight
258.27
MOL File
3562-99-0.mol
More
Less

Menbutone Property

Melting point:
172-173°
Boiling point:
361.52°C (rough estimate)
Density 
1.2105 (rough estimate)
refractive index 
1.4872 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO (Slightly), Methanol (Slightly, Sonicated), Ethanol (Slightly, Heated)
form 
Solid
pka
4.44±0.17(Predicted)
color 
White to Off-White
InChI
InChI=1S/C15H14O4/c1-19-14-8-6-11(13(16)7-9-15(17)18)10-4-2-3-5-12(10)14/h2-6,8H,7,9H2,1H3,(H,17,18)
InChIKey
FHGJSJFIQNQBCK-UHFFFAOYSA-N
SMILES
C12C=CC=CC1=C(OC)C=CC=2C(=O)CCC(=O)O
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

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

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

TRC
Product number
M218700
Product name
Menbutone
Packaging
1g
Price
$65
Updated
2021/12/16
ApexBio Technology
Product number
C6958
Product name
Menbutone
Packaging
100mg
Price
$80
Updated
2021/12/16
Matrix Scientific
Product number
089746
Product name
4-(4-Methoxynaphthalen-1-yl)-4-oxobutanoic acid
Purity
95+%
Packaging
5g
Price
$101
Updated
2021/12/16
ApexBio Technology
Product number
C6958
Product name
Menbutone
Packaging
200mg
Price
$130
Updated
2021/12/16
Matrix Scientific
Product number
089746
Product name
4-(4-Methoxynaphthalen-1-yl)-4-oxobutanoic acid
Purity
95+%
Packaging
1g
Price
$38
Updated
2021/12/16
More
Less

Menbutone Chemical Properties,Usage,Production

Uses

Menbutone is a cholerectic compound which is used for stimulating gastro-intestinal function by promoting secretory processes in animals including that of cattle, sheep, goats, horses and dogs. It is used in treatment of hepatic dysfunction of dogs by promoting bile secretion.

Originator

Hepalande, Delalande ,W. Germany ,1977

Uses

Menbutone is a cholerectic compound which is used for stimulating gastro-intestinal function by promoting secretory processes in animals including that of cattle, sheep, goats, horses and dogs. It is used in treatment of hepatic dysfunction of dogs by promoting bile secretion.

Definition

ChEBI: Menbutone is a butanone.

Manufacturing Process

395 parts of (α-methoxynaphthalene and 265 parts of succinic anhydride are dissolved in 8,000 parts of dry benzene at room temperature. The resulting solution is stirred and 710 parts of anhydrous aluminum chloride are added over a period of twenty minutes. During the addition the temperature of the reaction mixture rises to about 60°C to 70°C. After the addition the reaction mixture is stirred for fifteen or twenty minutes at 60°C to 70°C and then refluxed for one hour. The hot reaction mixture is then poured onto a mixture of 5,000 parts of ice and 900 parts of concentrated hydrochloric acid. The benzene is removed by steam distillation and the hot aqueous residue is filtered to remove the insoluble β-(1-methoxy-4-naphthoyl)-propionic acid. The residue of the latter is dried and then dissolved in 16,000 parts of hot water containing 300 parts of sodium carbonate. The hot solution is treated with activated charcoal, filtered while hot, chilled and acidified. The residue of purified acid is collected on a filter, washed with water, and dried at 65°C. A yield of 552 parts of purified β-(1-methoxy)-4-naphthoyl)propionic acid, melting at 172°C to 173°C is obtained.

Therapeutic Function

Choleretic

Synthesis

Menbutone is prepared by the reaction of succinic acid anhydride and 1-Methoxynaphthalene. The steps are as follows:
15.8 g of 1-methoxynaphthalene and 10.0 g of succinic anhydride were dissolved in 120 mL of dichloromethane,Stir, Cooling to 1 ~ 3 ° C, Divided into three batches of anhydrous aluminum trichloride 15.0 grams, The addition process takes about 20 minutes, The solution was then heated to 35 ± 2 ° C, Insulation reaction 6 hours (5.5 ~ 6.5 hours range), After the reaction is complete, The reaction solution was poured into an ice-water mixture (200 g of ice and 300 g of water) for 30 minutes,Standing, analysiscrystal, Filter, The filtrate was heated and distilled to recover dichloromethane, The cake is the crude of the ketone ketone; And then the crude ketoprofen water as a solvent by 2-3 times recrystallization, Activated carbon decolorization, Demon ketone boutique. The mass of the present product of the compound was 22.3 g, Melting point of 176 ~ 179 ° C, The yield was 86.4%.

Menbutone Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Menbutone Suppliers

Apin Chemicals Limited (UK)
Tel
--
Fax
--
Email
info@apinchemicals.com
Country
United Kingdom
ProdList
6184
Advantage
60
Leancare Ltd.
Tel
--
Fax
--
Email
enquiry@leancare.co.uk
Country
United Kingdom
ProdList
6446
Advantage
42
MOLEKULA Ltd.
Tel
--
Fax
--
Email
kevinbanks@molekula.com
Country
United Kingdom
ProdList
6140
Advantage
66
More
Less

View Lastest Price from Menbutone manufacturers

Henan Suikang Pharmaceutical Co.,Ltd.
Product
Menbutone 3562-99-0
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
99.0%
Supply Ability
1tons
Release date
2024-04-28
shandong perfect biotechnology co.ltd
Product
Menbutone 3562-99-0
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99% HPLC
Supply Ability
5 ton
Release date
2023-07-04

3562-99-0, MenbutoneRelated Search:


  • genabil
  • genabilicacid
  • genabilin
  • ido-genabil
  • menbuton
  • menbutone
  • naftobil
  • 3-(4-methoxy-1-naphthoyl)-propionicaci
  • 4-methoxy-gamma-oxo-1-naphthalenebutanoicaci
  • acidebeta-(1-methoxy-4-naphthoyl)propionique
  • beta-(1-methoxy-4-naphthoyl)-propionsaeure
  • epanaftol
  • fel-bis
  • nafto-epatina
  • P-METHOXYNAPHTHOYLPROPIONIC ACID
  • 3-(4-METHOXY-1-NAPHTHOYL)PROPIONIC ACID
  • Icteryl
  • SC 1749
  • 1-Methoxy-4-(.beta.-carboxyethylcarbonyl)-naphthalene
  • 4-keto-4-(4-methoxy-1-naphthyl)butyric acid
  • 4-(4-Methoxy-[1]naphthyl)-4-oxo-butyric acid
  • 1-Naphthalenebutanoic acid, 4-methoxy-g-oxo-
  • Meng Meng
  • 3-(4'-METHOXYNAPHTHOYL) PROPIONIC ACID
  • MENBUTONE STANDARD
  • 1-Naphthalenebutanoic acid, 4-methoxy-γ-oxo-
  • 3562-99-0 3-(4-METHOXY-1-NAPHTHOYL)PROPIONIC ACID C15H14O4
  • Meng cloth ketone
  • 3562-99-0
  • Aromatic Propionic Acids