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FLAVOXATE

Product Name
FLAVOXATE
CAS No.
15301-69-6
Chemical Name
FLAVOXATE
Synonyms
Uronid;Bladuril;FLAVOXATE;Flavoxate-d5;DW61 free base;FLAVOXATE USP/EP/BP;Rec-7-0040 free base;Piperidinoethyl 3-methyl-2-phenyl-4-oxo-4H-1-benzopyran-8-carboxylate;2-Piperidinoethyl 3-methyl-4-oxo-2-phenyl-4H-1-benzopyran-8-carboxylate;2-(1-Piperidinyl)ethyl 3-methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylate
CBNumber
CB2341499
Molecular Formula
C24H25NO4
Formula Weight
391.46
MOL File
15301-69-6.mol
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FLAVOXATE Property

Melting point:
87-88 °C
Boiling point:
564.1±50.0 °C(Predicted)
Density 
1.203±0.06 g/cm3(Predicted)
pka
7.3(at 25℃)
form 
Off-white solid.
CAS DataBase Reference
15301-69-6(CAS DataBase Reference)
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Safety

Toxicity
LD50 in rats (mg/kg): 1110 orally; 20.8 i.v. (Setnikar, 1975)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Biosynth Carbosynth
Product number
BF164464
Product name
Flavoxate
Packaging
50mg
Price
$43
Updated
2021/12/16
Biosynth Carbosynth
Product number
BF164464
Product name
Flavoxate
Packaging
250mg
Price
$105
Updated
2021/12/16
AK Scientific
Product number
E125
Product name
Flavoxate
Packaging
50mg
Price
$108
Updated
2021/12/16
AK Scientific
Product number
E125
Product name
Flavoxate
Packaging
250mg
Price
$191
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
RDL0006835
Product name
FLAVOXATE-D5
Purity
95.00%
Packaging
5MG
Price
$502.15
Updated
2021/12/16
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FLAVOXATE Chemical Properties,Usage,Production

Originator

Urispas,SKF,US,1971

Uses

Flavoxate is a pharmaceutical active-containing film delivery device for oral transmucosal administration.

Uses

Relaxant (smooth muscle).

Definition

ChEBI: A carboxylic ester resulting from the formal condensation of 3-methylflavone-8-carboxylic acid with 2-(1-piperidinyl)ethanol.

Manufacturing Process

A mixture of 13.3 grams of anhydrous aluminum chloride and 100 ml of carbon disulfide is added to 19.4 grams of 2-propionyloxybenzoic acid (prepared from the reaction of propionyl chloride and 2-hydroxybenzoic acid). After an initial evolution of hydrogen chloride, the solvent is removed by distillation and the mixture is heated at 150° to 160°C for 4 hours. The cooled reaction mixture is treated with ice and hydrochloric acid and the product, 2- hydroxy-3-carboxypropiophenone, is obtained from the oily residue by distillation in vacuo.
A mixture of 1.9 grams of 2-hydroxy-3-carboxypropiophenone, 5.0 grams of sodium benzoate and 20.0 grams of benzoic anhydride is heated at 180° to 190°C for 6 hours. A solution of 15.0 grams of potassium hydroxide in 50 ml of ethanol and 20 ml of water is added and refluxed for 1 hour. The mixture is evaporated and the residue after addition of water yields 3-methylflavone-8- carboxylic acid.
To a suspension of 12.0 grams of 3-methylflavone-8-carboxylic acid in 200 ml of anhydrous benzene is added 10.0 grams of thionyl chloride. The mixture is refluxed for 2 hours during which the suspended solid goes into solution. The solvent is completely removed by distillation, the residue extracted with benzene and the extract evaporated to dryness. The product, 3- methylflavone-8-carboxylic acid chloride, is recrystallized from ligroin to give crystals melting at 155° to 156°C.
To 11.0 grams of 3-methylflavone-8-carboxylic acid chloride dissolved in 150 ml of anhydrous benzene is added at room temperature 4.8 grams of piperidinoethanol and the mixture refluxed for 2 to 3 hours. The separated solid is filtered, washed with benzene and dried. The product, piperidinoethyl 3-methylflavone-8-carboxylate hydrochloride is obtained as a colorless crystalline solid, MP 232° to 234°C, (from US Patent 2,921,070).

brand name

Urispas (Ortho-McNeil).

Therapeutic Function

Spasmolytic

FLAVOXATE Preparation Products And Raw materials

Raw materials

Preparation Products

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FLAVOXATE Suppliers

Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9806
Advantage
58
LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
AdooQ Bioscience CHINA
Tel
025-58849295 18951903616;
Fax
025-68650336
Email
info@adooq.cn
Country
China
ProdList
2990
Advantage
60
Hubei Jusheng Technology Co.,Ltd
Tel
027-59599241 18871490274
Fax
027-59599241
Email
1400878000@qq.com
Country
China
ProdList
9958
Advantage
58
Shanghai Lollane Biological Technology Co.,Ltd.
Tel
021-52996696,15000506266 15000506266
Fax
+86-21-52996696
Country
China
ProdList
4456
Advantage
55
Aikon International Limited
Tel
025-66028182 18112977050
Fax
(3)02557626880
Email
cfzhang@aikonchem.com
Country
China
ProdList
15818
Advantage
58
Chengdu Saint - Kay Biotechnology Co., Ltd.
Tel
028-85157043 15882256948
Email
676046971@qq.com
Country
China
ProdList
4390
Advantage
58
Shanghai Han-Xiang Chemical Co., Ltd.
Tel
15971444841
Fax
18327183813
Email
amber@biochempartner.com
Country
China
ProdList
3061
Advantage
58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 +86-13028896684;
Email
sales@rrkchem.com
Country
China
ProdList
56902
Advantage
58
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View Lastest Price from FLAVOXATE manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
Flavoxate 15301-69-6
Price
US $1.00-1.00/KG
Min. Order
1g
Purity
99%
Supply Ability
50tons
Release date
2020-05-08

15301-69-6, FLAVOXATERelated Search:


  • FLAVOXATE
  • 2-(1-Piperidinyl)ethyl 3-methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylate
  • 2-Piperidinoethyl 3-methyl-4-oxo-2-phenyl-4H-1-benzopyran-8-carboxylate
  • 4H-1-Benzopyran-8-carboxylic acid, 3-methyl-4-oxo-2-phenyl-, 2-(1-piperidinyl)ethyl ester
  • 3-Methyl-4-oxo-2-phenyl-4H-1-benzopyran-8-carboxylic acid 2-piperidinoethyl ester
  • Piperidinoethyl 3-methyl-2-phenyl-4-oxo-4H-1-benzopyran-8-carboxylate
  • 2-(Piperidin-1-yl)ethyl 3-Methyl-4-oxo-2-phenyl-4H-chroMene-8-carboxylate
  • Flavoxate-d5
  • FLAVOXATE USP/EP/BP
  • Bladuril
  • Uronid
  • DW61 free base
  • Rec-7-0040 free base
  • 15301-69-6
  • 110153-71-2
  • C24H25NO4