benzilonium bromide

Product Name
benzilonium bromide
CAS No.
1050-48-2
Chemical Name
benzilonium bromide
Synonyms
Ortyn;Portyn;Partyn;PU 239;Ulcoban;Minelco;Minelsin;C.I. 379;Minelcin;Ortyn-d5
CBNumber
CB8897130
Molecular Formula
C22H28BrNO3
Formula Weight
434.36662
MOL File
1050-48-2.mol
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benzilonium bromide Property

Melting point:
203-204°
storage temp. 
Refrigerator
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
color 
Light Brown
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Safety

Toxicity
LD50 orally in rats: 1.86 g/kg (Reichertz, Schliva)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
B197000
Product name
rac-BenziloniumBromide
Packaging
50mg
Price
$1190
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0025401
Product name
BENZILONIUM BROMIDE
Purity
95.00%
Packaging
2MG
Price
$314
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0025401
Product name
BENZILONIUM BROMIDE
Purity
95.00%
Packaging
5MG
Price
$503.49
Updated
2021/12/16
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benzilonium bromide Chemical Properties,Usage,Production

Chemical Properties

Light Brown Solid

Originator

Pharm Chemical

Uses

An anticholinergic drug.

Manufacturing Process

A mixture containing of 23 g of 1-ethyl-3-hydroxypyrrolidine, 51.2 g of ethylbenzilate and 1.50 ml of benzene is subjected to azeotropic distillation to remove traces of water and then 250 mg of metallic sodium added to the residual solution. The mixture heated under reflux for about 8 hours while slowly drawing off the benzene-alcohol azeotrope formed. The reaction mixture is cooled, treated with 1 ml of acetic acid and washed with water. The benzene is removed by distillation and the residue distilled in vacuo to obtain the desired 1-ethyl-3-pyrrolidinyl benzilate as a viscous oil; yield 44 g, 68.1%; b.p. 164-170°C at 0.2 mm.
If desired, this same product can be prepared by adding 8 g of 1-ethyl-3- hydroxypyrrolidine in about 40 ml of dry methylene dichloride to 18.4 g of diphenylchloroacetyl chloride in about 40 ml of boiling methylene dichloride and refluxing the mixture for 1 hour. The solvent is evaporated and the residue heated on a steam bath with 200 ml of water for 5 min and then allowed to stand at room temperature for 2 days. The mixture is treated with potassium carbonate, extracted with benzene and the benzene distilled from the extract to obtain crude l-ethyl-3-pyrrolidinyl benzilate. Distillation in vacuo yields the pure l-ethyl-3-pyrrolidinyl benzilate; yield 8 g (31%); b.p. 197°C at 2 mm.
22 g of 1-ethyl-3-pyrrolidinyl benzilate prepared by either of the above methods is mixed with 32 g of ethyl bromide in 100 ml of isopropanol and refluxed for 1 hour to give 23 g of 1,1-diethyl-3-pyrrolidinium bromide benzilate, m.p.196-197°C.

brand name

Portyn (Parke-Davis).

Therapeutic Function

Anticholinergic

benzilonium bromide Preparation Products And Raw materials

Raw materials

Preparation Products

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benzilonium bromide Suppliers

United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
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View Lastest Price from benzilonium bromide manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
benzilonium bromide 1050-48-2
Price
US $0.10/KG
Min. Order
1KG
Purity
98.0%
Supply Ability
10
Release date
2024-07-07

1050-48-2, benzilonium bromideRelated Search:


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