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550-99-2

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550-99-2 Usage

Pharmacological effects

Naphazoline hydrochloride, is commonly used as a vasoconstrictor in the hospital's otorhinolaryngology and ophthalmology ,it is a adrenomimetic drug ,it has a strong effect on contraction of blood vessels and blood pressure elevation,it has inhibition effect on the central nervous system,by contraction of local vascular, it can play an anti-inflammatory and analgesic role in the local inflammatory lesions , and can eliminate congestion due to fatigue or other reasons. Clinically it is used for the treatment of colds, acute and chronic rhinitis, allergic conjunctivitis, allergic and inflammatory nasal congestion embolism. Local long-term use can lead to blood flow reduction in medication area, which causes resistance decreasing , and results in superinfection. It can not be taken orally. Dropping excess liquid or high concentrations can cause poisoning. Care should be taken, especially in children. Infants, hypertension, hyperthyroidism patients should take with caution, atrophic rhinitis patients are banned. The interval time of dropping , is preferably not less than 4 to 6 hours. The above information is edited by the lookchem of Tian Ye.

Chemical Properties

Different sources of media describe the Chemical Properties of 550-99-2 differently. You can refer to the following data:
1. White crystalline powder. Melting point 255-260 ℃. 40 grams of the product can be dissolved in 100 ml of water . It is soluble in alcohol, slightly soluble in chloroform, insoluble in ether and benzene. Odorless, bitter taste.
2. White or almost white, crystalline powder.

Uses

Different sources of media describe the Uses of 550-99-2 differently. You can refer to the following data:
1. This product is a vasoconstrictor. Rat subcutaneous injection is LD50 385 mg/kg.
2. Naphazoline Hydrochloride is a useful synthetic intermediate used in eye drops. A vasoconstrictor.

Production method

By the α-naphthalene acetic acid and ethylene diamine condensation, cyclization ,2-(1-naphthylmethyl) imidazoline (C14H14N2, [835-31-4]) is made , then after salifying, naphazoline hydrochloride is derived . The α-acetic acid and ethylene diamine are added to the reaction pot, stir and heat to 120 ℃, react after 1 hour, then heat to 130 ℃, react for 1 hour. Ethylenediamine and water are distilled ,and after vacuum distillation, collect 180-240 ℃ (1.33-4 kPa) distillate, obtain 2-(1-naphthylmethyl) imidazoline. It is dissolved in a mixture of acetone and ethanol, and at 10-12℃ inlet hydrogen chloride gas to become into a salt, naphazoline hydrochloride crystals is generated .

Originator

Albalon,Allergan,Australia

Manufacturing Process

2.7 parts of naphtyl-(1)-acetiminoethylether (produced from naphthyl-1- acetonitrile) were dissolved in 12 parts of absolute alcohol. 1 part of ethylenediamine is then added and the mixture was heated to gentle boiling while passing it through nitrogen and simultaneously stirring until ammonia escaped no longer. The alcohol was is then distilled and the residue mixed with 40 parts of benzene and 1.8 parts of caustic potash. Stirring was continued for some time whereby the imidazoline base was dissolved in benzene. The benzene residue, is recrystallized several times from toluene. The 2-[naphthyl-1-methyl]-imidazoline represented the coloriless crystalls of melting point 252°-253°C. Its hydrochloride is easily soluble in water.

Brand name

Albalon (Allergan); Nafazair (Bausch & Lomb); Nafazair (Pharmafair); Naphcon (Alcon); Opcon (Bausch & Lomb); Vasocon (Novartis).

Therapeutic Function

Vasoconstrictor, Nasal decongestant

Check Digit Verification of cas no

The CAS Registry Mumber 550-99-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 550-99:
(5*5)+(4*5)+(3*0)+(2*9)+(1*9)=72
72 % 10 = 2
So 550-99-2 is a valid CAS Registry Number.

550-99-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (N0542)  Naphazoline Hydrochloride  >99.0%(T)

  • 550-99-2

  • 10g

  • 290.00CNY

  • Detail
  • Alfa Aesar

  • (B24161)  2-(1-Naphthylmethyl)-2-imidazoline hydrochloride, 99%   

  • 550-99-2

  • 25g

  • 349.0CNY

  • Detail
  • Alfa Aesar

  • (B24161)  2-(1-Naphthylmethyl)-2-imidazoline hydrochloride, 99%   

  • 550-99-2

  • 100g

  • 1045.0CNY

  • Detail
  • Alfa Aesar

  • (B24161)  2-(1-Naphthylmethyl)-2-imidazoline hydrochloride, 99%   

  • 550-99-2

  • 500g

  • 4183.0CNY

  • Detail
  • Sigma-Aldrich

  • (N0080000)  Naphazolinehydrochloride  European Pharmacopoeia (EP) Reference Standard

  • 550-99-2

  • N0080000

  • 1,880.19CNY

  • Detail
  • USP

  • (1457006)  Naphazoline hydrochloride  United States Pharmacopeia (USP) Reference Standard

  • 550-99-2

  • 1457006-200MG

  • 4,662.45CNY

  • Detail
  • Sigma

  • (N5504)  Naphazolinehydrochloride  

  • 550-99-2

  • N5504-25G

  • 617.76CNY

  • Detail

550-99-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Naphazoline hydrochloride

1.2 Other means of identification

Product number -
Other names 1H-Imidazole, 4,5-dihydro-2-(1-naphthalenylmethyl)-, monohydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:550-99-2 SDS

550-99-2Synthetic route

naphazoline
835-31-4

naphazoline

naphazoline hydrochloride
550-99-2

naphazoline hydrochloride

Conditions
ConditionsYield
With hydrogenchloride In acetonitrile at 20℃; Solvent; Large scale;92.33%
With hydrogenchloride In acetone at 5℃; for 0.5h; pH=1; Temperature; Reflux;

550-99-2Upstream product

550-99-2Downstream Products

550-99-2Relevant articles and documents

Preparation method of naphazoline hydrochloride

-

Paragraph 0015-0022, (2021/01/24)

The invention relates to the technical field of organic synthesis, in particular to a preparation method of naphazoline hydrochloride, which comprises the following steps: by using alpha-naphthylacetic acid, ethylenediamine and acetone as raw materials, carrying out condensation, cyclization, salification and the like to prepare 4, 5-dihydro-2-(1-naphthyl methyl)-1H-imidazole hydrochloride. Alpha-naphthylacetic acid, ethylenediamine and acetone are used as raw materials to prepare the target product, and the raw materials are easy to obtain and low in price. Condensation, cyclization and salification are adopted, the operation reaction conditions are mild, a large number of side reactions are avoided, and the high yield is obtained. The preparation process is high in coherence, short in time consumption and more efficient and thorough in reaction. The preparation process is simple, reaction conditions are mild, and environmental pollution is avoided.

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