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(4E)-4-1-[(4-methoxyphenyl)amino]ethylidene-1-phenylpyrazolidine-3,5-dione, commonly known as Ketorolac, is a non-steroidal anti-inflammatory drug (NSAID) characterized by its potent pain-relieving and anti-inflammatory properties. It operates by inhibiting the synthesis of prostaglandins, which are chemicals responsible for inducing pain and inflammation within the body. Ketorolac is recognized for its effectiveness in managing a range of conditions, from post-surgical discomfort to chronic diseases like arthritis.

80141-82-8

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80141-82-8 Usage

Uses

Used in Pain Management:
Ketorolac is utilized as an analgesic agent for the treatment of moderate to severe pain. It is particularly effective in postoperative pain management and is also prescribed for conditions such as arthritis, where inflammation and pain are significant concerns. The drug's ability to reduce prostaglandins makes it a valuable asset in the medical field for pain relief.
Used in Anti-inflammatory Applications:
Beyond its analgesic properties, Ketorolac serves as an anti-inflammatory agent, mitigating the inflammation associated with various conditions. This dual action makes it a versatile choice for healthcare professionals when addressing issues that involve both pain and inflammation.
Used in Pharmaceutical Formulations:
Ketorolac is available in multiple formulations, including oral tablets, injectable solutions, and ophthalmic solutions, allowing for a range of administration options to suit different patient needs and preferences. Its versatility in formulation contributes to its widespread use in clinical settings.
Used in Acute Pain Relief:
Due to its potent effects, Ketorolac is often prescribed for short-term use to provide rapid relief from acute pain. It is crucial to follow the guidance of healthcare professionals when using Ketorolac to avoid potential side effects and interactions with other medications.
Used in the Medical Industry:
In the medical industry, Ketorolac is used as a potent analgesic and anti-inflammatory agent for various painful and inflammatory conditions. Its effectiveness in managing postoperative pain and conditions like arthritis makes it a staple in the treatment arsenal of healthcare providers.
Used in the Pharmaceutical Industry:
Within the pharmaceutical industry, Ketorolac is used in the development and production of medications aimed at providing relief from pain and inflammation. Its formulation in different dosages and forms allows for targeted treatment options, enhancing patient care and satisfaction.

Check Digit Verification of cas no

The CAS Registry Mumber 80141-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,1,4 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80141-82:
(7*8)+(6*0)+(5*1)+(4*4)+(3*1)+(2*8)+(1*2)=98
98 % 10 = 8
So 80141-82-8 is a valid CAS Registry Number.

80141-82-8SDS

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 (4E)-4-[1-(4-methoxyanilino)ethylidene]-1-phenylpyrazolidine-3,5-dione

1.2 Other means of identification

Product number -
Other names -

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:80141-82-8 SDS

80141-82-8Downstream Products

80141-82-8Relevant academic research and scientific papers

ETUDE DU COMPORTEMENT CHIMIQUE DE PYRANOPYRAZOLE-3(2H)-ONES VIS-A-VIS DES BASES AZOTEES. I. Reaction avec les amines aromatiques.

Maquestiau, A.,Haverbeke, Y. van,Eynde, J. J. vanden

, p. 963 - 970 (2007/10/02)

2-phenyl-4,6-dimethylpyranopyrazole-3(2H)-one reacts with arylamines to form arylaminoethylidenepyrazolidin-3,5-diones.The reaction pathway is highly dependent on the nature of the arylamine.

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