Welcome to LookChem.com Sign In|Join Free
  • or
Benzenepropanoic acid, 4-(1H-imidazol-1-ylmethyl)-, commonly known as ibuprofen, is a nonsteroidal anti-inflammatory drug (NSAID) that is widely used for its analgesic, antipyretic, and anti-inflammatory properties. It functions by inhibiting the production of prostaglandins, which are chemicals responsible for pain and inflammation. Ibuprofen is available both over the counter and in prescription strength, making it accessible for a range of conditions.

103549-17-3

Post Buying Request

103549-17-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

103549-17-3 Usage

Uses

Used in Pain Relief Applications:
Ibuprofen is used as a pain reliever for various conditions such as headaches, muscle aches, and menstrual cramps. Its ability to reduce inflammation and alleviate pain makes it a popular choice for managing mild to moderate pain.
Used in Antipyretic Applications:
Ibuprofen is employed as an antipyretic to reduce fever by lowering the body's temperature. It is particularly useful in cases of fever caused by inflammation or infection.
Used in Inflammation Management Applications:
Ibuprofen is utilized to manage inflammation associated with conditions such as arthritis. It helps to decrease the swelling and discomfort caused by the inflammation, improving the quality of life for individuals suffering from these conditions.
Used in Over-the-Counter Medications:
Ibuprofen is a key ingredient in many over-the-counter medications designed to treat pain, fever, and inflammation. Its widespread availability and effectiveness make it a common choice for self-treatment of various ailments.
Used in Prescription Strength Medications:
For individuals requiring a higher dosage or those with more severe conditions, ibuprofen is available in prescription strength. This allows healthcare professionals to tailor the treatment to the specific needs of the patient.
Used in Healthcare Professional Guidance:
Due to potential side effects and contraindications, particularly for individuals with a history of cardiovascular disease, ibuprofen should be used under the guidance of a healthcare professional. This ensures that the medication is used safely and effectively, minimizing the risk of adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 103549-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,4 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103549-17:
(8*1)+(7*0)+(6*3)+(5*5)+(4*4)+(3*9)+(2*1)+(1*7)=103
103 % 10 = 3
So 103549-17-3 is a valid CAS Registry Number.

103549-17-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[p-(1H-imidazole-1-ylmethyl)phenyl]propionic acid

1.2 Other means of identification

Product number -
Other names 3-(4-Imidazol-1-ylmethyl-phenyl)-propionic acid

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:103549-17-3 SDS

103549-17-3Downstream Products

103549-17-3Relevant academic research and scientific papers

Highly selective inhibitors of thromboxane synthetase. 1. Imidazole derivatives

Iizuka,Akahane,Momose,Nakazawa,Tanouchi,Kawamura,Ohyama,Kajiwara,Iguchi,Okada,Taniguchi,Miyamoto,Hayashi

, p. 1139 - 1148 (2007/10/02)

The structure-activity relationships of imidazole derivatives as inhibitors of thromboxane (TX) synthetase were investigated. Introduction of various substituents (e.g., one or two methyl groups, a halogen atom, a methylidene group, unsaturated bonds, or a phenylene group) into the α position or other positions in the carboxy-bearing side chain of 1-(7-carboxyheptyl)imidazole was found to increase the inhibitory potency. The length of the side chains with the phenylene group was optimum for the inhibitory potency on TX synthetase in the region of 8.5-9.0 A. Among the tested imidazole derivatives, 1-(7-carboxy-7-methyl-2-octynyl)imidazole, 4-[3-(1-imidazolyl)-propyl]benzoic acid, and (E)-4-(1-imidazolylmethyl)cinnamic acid and its α-methyl analogue showed the highest potency with an IC50 in the range of 10-8 to 10-9 M. Inhibition by these derivatives was highly selective for the TX synthetase, since other enzymes such as fatty acid cyclo-oxygenase and prostacyclin synthetase were not affected.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 103549-17-3