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Levalbuterol Related Compound B (20 mg) (alpha-[(1,1-Dimethylethyl)aminomethyl]-4-hydroxy-3-methyl-benzenemethanol) is a chemical compound derived from the parent drug Levalbuterol, which is a selective stimulant of β-adrenergic receptors in bronchial muscles. It is used as an impurity reference standard for the quality control of pharmaceutical products and is also known as 3-Dehydroxy Salbutamol (Levalbuterol USP Related Compound B; Salbutamol EP Impurity C).

18910-68-4

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18910-68-4 Usage

Uses

Used in Pharmaceutical Quality Control:
Levalbuterol Related Compound B (20 mg) (alpha-[(1,1-Dimethylethyl)aminomethyl]-4-hydroxy-3-methyl-benzenemethanol) is used as an impurity reference standard for the quality control of pharmaceutical products, specifically for Levalbuterol, which is a medication used in the treatment of asthma and other respiratory conditions. Its application ensures the safety, efficacy, and purity of the final drug product.
Used in Research and Development:
In the field of pharmaceutical research and development, Levalbuterol Related Compound B (20 mg) (alpha-[(1,1-Dimethylethyl)aminomethyl]-4-hydroxy-3-methyl-benzenemethanol) serves as a valuable reference compound for the synthesis, characterization, and optimization of new drugs targeting β-adrenergic receptors. Its use in research helps in understanding the structure-activity relationship of these receptors and contributes to the development of more effective and safer medications for respiratory diseases.
Used in Regulatory Compliance:
Levalbuterol Related Compound B (20 mg) (alpha-[(1,1-Dimethylethyl)aminomethyl]-4-hydroxy-3-methyl-benzenemethanol) is also utilized in the regulatory compliance process for pharmaceutical manufacturers. It helps in meeting the regulatory requirements for drug quality, safety, and efficacy, ensuring that the final drug product meets the necessary standards before being released to the market.

Check Digit Verification of cas no

The CAS Registry Mumber 18910-68-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,1 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18910-68:
(7*1)+(6*8)+(5*9)+(4*1)+(3*0)+(2*6)+(1*8)=124
124 % 10 = 4
So 18910-68-4 is a valid CAS Registry Number.

18910-68-4 Well-known Company Product Price

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  • USP

  • (1012644)  Albuterol Related Compound A  United States Pharmacopeia (USP) Reference Standard

  • 18910-68-4

  • 1012644-25MG

  • 14,500.98CNY

  • Detail
  • USP

  • (1358809)  Levalbuterol Related Compound B  United States Pharmacopeia (USP) Reference Standard

  • 18910-68-4

  • 1358809-20MG

  • 13,501.80CNY

  • Detail

18910-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(tert-butylamino)-1-hydroxyethyl]-2-methylphenol

1.2 Other means of identification

Product number -
Other names UNII-152NRR02YD

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:18910-68-4 SDS

18910-68-4Downstream Products

18910-68-4Relevant academic research and scientific papers

Preparation method and application of salbutamol impurity

-

Paragraph 0064-0081, (2021/06/22)

The invention discloses a preparation method and application of a salbutamol impurity. The preparation method adopts the following process route of taking 2-acetoxy-5-(2-bromoacetyl) benzyl acetate (ABBA) as an initial raw material, and firstly reacting w

A Combined High-Throughput Screening and Reaction Profiling Approach toward Development of a Tandem Catalytic Hydrogenation for the Synthesis of Salbutamol

Leitch, David C.,Greene, Thomas F.,O'Keeffe, Roisin,Lovelace, Thomas C.,Powers, Jeremiah D.,Searle, Andrew D.

supporting information, p. 1806 - 1814 (2017/11/24)

A combined high-throughput screening and reaction profiling approach to the telescoping of two reductions in the synthesis of Salbutamol is described. Optimization studies revealed the beneficial effect of mildly acidic conditions, and the use of water as a cosolvent. Persistent formation of deoxygenated impurities using a Pd/C catalyst led to the initiation of reaction profiling studies, which revealed that the ketone intermediate formed after rapid debenzylation is the sole source of deoxygenated impurities, indicating that more rapid ketone hydrogenation should minimize this deoxygenation. A dual catalyst approach based on these insights has been developed, with both Pd/Pt and Ru/Pt catalyst systems as more selective than Pd-only systems. Based on reaction profiles that indicate the deoxygenation side reaction is first-order in the concentration of debenzylated ketone intermediate, Pt catalysts for rapid and selective ketone hydrogenation were paired with Pd and Ru catalysts known to perform selective debenzylation. Optimization of these dual catalyst processes led to conditions that were demonstrated on 20 g scale to prepare Salbutamol in 49% isolated yield after recrystallization.

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