ChemicalBook > Product Catalog >Biochemical Engineering >Inhibitors >Neuronal Signaling >COX inhibitors >Ketorolac tromethamine

Ketorolac tromethamine

Ketorolac tromethamine Structure
CAS No.
74103-07-4
Chemical Name:
Ketorolac tromethamine
Synonyms
syntex;Ketorolac (Toradol);Ketorolac Thromethamine;KETOROLAC TROMETHAMINE SALT;Godek;TORADOL;Ketanov;Ketorol;Tarazyn;Acular ls
CBNumber:
CB2427540
Molecular Formula:
C19H24N2O6
Molecular Weight:
376.41
MOL File:
74103-07-4.mol
MSDS File:
SDS
Modify Date:
2025/2/14 15:59:18

Ketorolac tromethamine Properties

Melting point 160-161 C
storage temp. 2-8°C
solubility H2O: 15 mg/mL stable at least one month at −20 °C., soluble
form crystalline
color White to Light yellow
biological source synthetic (organic)
Water Solubility H2O: soluble 15mg/mL, clear, colorless to faintly yellow (stable at least one month at -20 °C.)
λmax 322nm(MeOH)(lit.)
Merck 14,5306
Stability Hygroscopic
InChI InChI=1S/C15H13NO3.C4H11NO3/c17-14(10-4-2-1-3-5-10)13-7-6-12-11(15(18)19)8-9-16(12)13;5-4(1-6,2-7)3-8/h1-7,11H,8-9H2,(H,18,19);6-8H,1-3,5H2
InChIKey BWHLPLXXIDYSNW-UHFFFAOYSA-N
SMILES C(N)(CO)(CO)CO.C(C1C=CC=CC=1)(C1=CC=C2C(C(=O)O)CCN12)=O
CAS DataBase Reference 74103-07-4(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06
Signal word  Danger
Hazard statements  H301-H315-H319-H335
Precautionary statements  P301+P310+P330-P302+P352-P305+P351+P338
Hazard Codes  T
Risk Statements  25-36/37/38-23/24/25
Safety Statements  26-45-36/37/39
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  UY7759900
HazardClass  6.1(a)
PackingGroup  II
HS Code  2933995500
NFPA 704
0
2 0

Ketorolac tromethamine price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) PHR1140 Ketorolac Tromethamine Pharmaceutical Secondary Standard; Certified Reference Material 74103-07-4 500MG ₹10002.3 2022-06-14 Buy
Sigma-Aldrich(India) K1136 Ketorolac tris salt ≥99%, crystalline 74103-07-4 1G ₹15187.48 2022-06-14 Buy
Sigma-Aldrich(India) K1136 Ketorolac tris salt ≥99%, crystalline 74103-07-4 5G ₹50909.98 2022-06-14 Buy
TCI Chemicals (India) K0053 Ketorolac Tromethamine 74103-07-4 1G ₹5100 2022-05-26 Buy
TCI Chemicals (India) K0053 Ketorolac Tromethamine 74103-07-4 5G ₹18900 2022-05-26 Buy
Product number Packaging Price Buy
PHR1140 500MG ₹10002.3 Buy
K1136 1G ₹15187.48 Buy
K1136 5G ₹50909.98 Buy
K0053 1G ₹5100 Buy
K0053 5G ₹18900 Buy

Ketorolac tromethamine Chemical Properties,Uses,Production

Description

Ketorolac tromethamine is a nonsteroidal antiinflammatory agent that exhibits analgesic and antipyretic activity. The compound is effective in the management of moderate to severe postoperative pain. It is, however, the first of this type of agent to be administered parenterally as an analgesic and is specifically indicated for intramuscular injection. Ketorolac represents a useful alternative to the narcotic analgesics due to its lack of abuse potential.

Chemical Properties

A carboxylic acid derivative nonsteroidal antiinflammatory agent, ketorolac tromethamine occurs as an off-white crystalline powder with a pKa of 3.54 (in water). More than 500 mg are soluble in one mL of water at room temperature. The commercially available injection is a clear, slightly yellow solution with a pH of 6.9 – 7.9. Sodium chloride is added to make the solution isotonic. Ketorolac tromethamine may also be known as RS-37619-00- 31-3; many trade names are available.

Uses

Cyclo-oxygenase inhibitor; analgesic; anti-inflammatory.

Indications

Ketorolac tromethamine is a pyrrolol-pyrrole nonsteroidal anti- inflammatory agent that inhibits prostaglandin formation. Prostaglandins mediate inflammation within the eye by disrupting the blood-aqueous barrier, inducing vasodilation and increasing intraocular pressure. Prostaglandins may also cause iris sphincter constriction (miosis) independent of cholinergic mechanisms. Ketorolac tromethamine is marketed for use before cataract extraction in human patients (to prevent miosis during surgery) and for control of post surgical inflammation, especially following cataract surgery. It is also approved for management of conjunctivitis associated with seasonal allergy in people. In veterinary medicine, ketorolac tromethamine is primarily used to control surgical or nonsurgical uveitis particularly in cases with concurrent corneal bacterial infection or ulceration when topical corticosteroids are contraindicated. It is also used in diabetic patients, especially smaller patients, adversely affected by systemic uptake of topically applied corticosteroids. Nonsteroidal agents like ketorolac tromethamine can be combined with topical steroids in patients with severe uveal inflammation.

Definition

ChEBI: An organoammonium salt resulting from the mixture of equimolar amounts of ketorolac and tromethamine (tris). It has potent non-sedating analgesic and moderate anti-inflammatory effects. It is used in the short-term management of post-operative pain, and in eye drops to relieve the ocular itching associated with seasonal allergic conjunctivitis.

General Description

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. Ketorolac Tromethamine belongs to the class of non-steroidal anti-inflammatory drugs, and its mode of action involves the inhibition of the bodily synthesis of prostagladins. It exhibits anti-inflammatory, antipyretic and analgesic effects.

Pharmacokinetics

After oral administration, ketorolac is rapidly absorbed; in dogs peak levels occur in about 50 minutes and oral bioavailability is about 50 – 75%.
Ketorolac is distributed marginally through the body. It does not appear to cross the blood-brain barrier and is highly bound to plasma proteins (99%). The volume of distribution in dogs is reported to be about 0.33 – 0.42 L/kg (similar in humans). The drug does cross the placenta.
Ketorolac is primarily metabolized via glucuronidation and hydroxylation. Both unchanged drug and metabolites are excreted mainly in the urine. Patients with diminished renal function will have longer elimination times than normal. In normal dogs, the elimination half-life is between 4 – 8 hours.

Pharmacology

Like other NSAIDs, ketorolac exhibits analgesic, antiinflammatory, and antipyretic activity probably through its inhibition of cyclooxygenase with resultant impediment of prostaglandin synthesis. Ketorolac may exhibit a more potent analgesic effect than some other NSAIDs. It inhibits both COX-1 and COX-2 receptors.

Side effects

The manufacturer indicates that ketorolac tromethamine does not enhance the spread of preexisting corneal fungal, viral or bacterial infections in animal models. Ketorolac tromethamine does not in and of itself induce postoperative pressure elevation other then that which frequently follows cataract extraction in people and animals.

Safety Profile

Ketorolac does cross the placenta. In humans, the FDA categorizes this drug as category C for use during the first two trimesters of pregnancy (Animal studies have shown an adverse effect on the fetus, but there are no adequate studies in humans; or there are no animal reproduction studies and no adequate studies in humans.) In humans, all NSAIDs are assigned to category D for use during pregnancy during the third trimester or near delivery (There is evidence of human fetal risk, but the potential benefits from the use of the drug in pregnant women may be acceptable despite its potential risks.) Most NSAIDs are excreted in milk. Ketorolac was detected in human breast milk at a maximum milk:plasma ratio of 0.037. It is unlikely to pose great risk to nursing offspring.

Overdosage

Limited information is available. The oral LD50 is 200 mg/kg in mice. GI effects, including GI ulceration are likely in overdoses in small animals. Metabolic acidosis was reported in one human patient. Consider GI emptying in large overdoses; patients should be monitored for GI bleeding. Treat ulcers with sucralfate; consider giving misoprostol early.

Precautions

Ketorolac is relatively contraindicated in patients with a history of, or preexisting, hematologic, renal or hepatic disease. It is contraindicated in patients with active GI ulcers or with a history of hypersensitivity to the drug. It should be used cautiously in patients with a history of GI ulcers, or heart failure (may cause fluid retention), and in geriatric patients. Animals suffering from inflammation secondary to concomitant infection, should receive appropriate antimicrobial therapy. Because ketorolac has a tendency to cause gastric erosion and ulcers in dogs, long-term use (>3 days) is not recommended in this species.

Global( 470)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
VASISTA LIFE SCIENCES PRIVATE LIMITED +91-04029554774 +91-9010855544 Hyderabad, India 153 58 Inquiry
Dr. Reddy's Laboratories Ltd +91-4049002900 +91-4049002900 Hyderabad, India 165 58 Inquiry
SNECOFRi Pvt Ltd +91-9032850129 +91-9032850129 Telangana, India 403 58 Inquiry
Gonane Pharma +91-9819380043 +91-9819380043 NaviMumbai, India 192 58 Inquiry
Vivimed Labs Ltd +914066086608 Telangana, India 61 58 Inquiry
Hetero Drugs Limited +91-4023704923 +91-4023704923 Telangana, India 296 58 Inquiry
Nosch Labs Pvt Ltd +91-4048557474 +91-9948222287 Hyderabad, India 58 58 Inquiry
Viyash Life Sciences Pvt Ltd +91-4023635052 +91-4023635052 Telangana, India 213 58 Inquiry
Shamrock Medicaments Ltd. +91-9167620304 +91-9167620304 Mumbai, India 16 58 Inquiry
Humble Healthcare Limited +91-9720093000 +91-8006400378 Uttar Pradesh, India 140 58 Inquiry

Related articles

Ketorolac tromethamine Spectrum

KETOROLAC TRIS SALT KETOROLAC TROMETHAMINE (+/-)-5-BENZOYL-2,3-DIHYDRO-1H-PYRROLIZINE-1-CARBOXYLIC ACID, TRIS (HYDROXYMETHYL) AMINOMETHANE SALT (+/-)-5-benzoyl-2,3-dihydro-1h-pyrrolizine-1-carboxylic acid tris(hydroxymethyl)methylamine salt (+/-)-5-BENZOYL-2,3-DIHYDRO-1H-PYRROLIZINE-1-CARBOXYLIC ACID TRIS SALT KETROLAC TROMETHAMINE SALT (±)-Form tromethamine salt KEROROLACTROMETHAMINE KETOROLACTROMETHAMINE,USP TORADOL TORADOL TRIS SALT 3-dihydro-5-benzoyl-(+-)-compd.with2-1h-pyrrolizine-1-carboxylicaci amino-2-(hydroxymethyl)-1,3-propanediol(1:1) 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid,compd. with 2-amino-2-(hydroxymethyl)-1,3-propanediol (1:1) Ketorolac Tromethamine (200 mg)G1E3311.000mg/mg(dr) Toradol, (±)-5-Benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid tris salt Acular ls Acular pf Acular preservative free Godek Tromethamine ketorolac Ketorolac tris salt,(±)-5-Benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid tris salt, Toradol Ketorolac Tromethamine (200 mg) rac Ketorolac TroMethaMine Salt Ketanov Ketorol Tarazyn TroMetaMol Ketorolac KETOROLAC TROMETHAMINE REFERENCE STANDARD 2-amino-2-(hydroxymethyl)propane-1,3-diol 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylate 2-Amino-2-(hydroxymethyl)propane-1,3-diol (1RS)-5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylate Toradol,Ketorolac Tromethamine 2-hydroxyethyl-bis(hydroxymethyl)ammonium Ketorolac tromethamine salt (RS37619 tromethamine salt) KetorolacTromethamine> Ketorolac Trometamol/ Ketorolac Tromethamine Ketorolac tromethamine (RS37619 tromethamine) Ketorolac Tromethamine (1356665) Angioamin KETOROLAC TROMETHAMINE SALT syntex Ketorolac (Toradol) Ketorolac Thromethamine KETOROLAC TROMETHAMINE (Inj. Gr.) methyl (1RS)-5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylate ethyl (1RS)-5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylate (±)-5-BENZOYL-2,3-DIHYDRO-1HPYRROLIZINE-1-CARBOXYLIC ACID,2-AMINO- 2-HYDROXYMETHYL)-1,3-PROPANEDIOL Ketorolac Impurity 9 Tromethamine Ketorolac Tromithamine Ketorolac tramine Ketorolac tromethamine impurity-2 KETOROLAC TROMETHAMINE TABLET/INJ Ketorolac tromethamine, COX-1 inhibitor Ketorolac tromethamine salt, 10 mM in DMSO 74103-07-4 74103-07- 74103-70-9 C15H13NO3.C4H11NO3