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Tapentadol Hydrochloride

CAS No.
175591-09-0
Chemical Name:
Tapentadol Hydrochloride
Synonyms
Tapentediol;Tapentadol hcl;Tapentadol Hydrochloride;Tapentadol (hydrochloride) (CRM);Tapentadol hydrochloride solution;Tapentadol hydrochloride(Y0002120);3-[(1R,2R)-3-(DiMethylaMino)-1-ethyl-2-Methylpro;Tapentadol Hydrochloride (1.0 mg/mL in Methanol);3-((2R,3R)-1-(diMethylaMino)-2-Methylpentan-3-yl)phenol hydrochloride;3-[(1R,2R)-3-(Dimethylamino)-1-ethyl-2-methylpropyl]phenol Hydrochloride
CBNumber:
CB71565532
Molecular Formula:
C14H24ClNO
Molecular Weight:
257.81
MDL Number:
MFCD00944992
MOL File:
175591-09-0.mol
Last updated:2023-11-02 15:05:42

Tapentadol Hydrochloride Properties

Melting point 178-194°C
Flash point 9℃
storage temp. -20°C Freezer, Under Inert Atmosphere
solubility DMF: 20 mg/ml; DMSO: 25 mg/ml; Ethanol: 20 mg/ml; PBS (pH 7.2): 10 mg/ml
form A neat solid
NCI Dictionary of Cancer Terms tapentadol hydrochloride
FDA UNII 71204KII53

Pharmacokinetic data

Protein binding 20%
Excreted unchanged in urine 3%
Volume of distribution 442-638 Litres
Biological half-life 4 (SR: 5-6) / Probably increased

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS06,GHS08
Signal word  Danger
Hazard statements  H225-H301+H311+H331-H370
Precautionary statements  P210-P260-P280-P301+P310-P311
Hazard Codes  F,T
Risk Statements  11-23/24/25-39/23/24/25
Safety Statements  7-16-36/37-45
RIDADR  UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany  1
NFPA 704
0
2 0

Tapentadol Hydrochloride price More Price(7)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich T-058 Tapentadol hydrochloride solution 1.0?mg/mL in methanol (as free base), ampule of 1?mL, certified reference material, Cerilliant? 175591-09-0 1mL $253 2024-03-01 Buy
Cayman Chemical 9000620 Tapentadol (hydrochloride) ≥98% 175591-09-0 1mg $81 2024-03-01 Buy
Cayman Chemical 18660 Tapentadol (hydrochloride) (CRM) 175591-09-0 1mg $171 2024-03-01 Buy
Cayman Chemical 9000620 Tapentadol (hydrochloride) ≥98% 175591-09-0 5mg $184 2024-03-01 Buy
Cayman Chemical 9000620 Tapentadol (hydrochloride) ≥98% 175591-09-0 50mg $1145 2024-03-01 Buy
Product number Packaging Price Buy
T-058 1mL $253 Buy
9000620 1mg $81 Buy
18660 1mg $171 Buy
9000620 5mg $184 Buy
9000620 50mg $1145 Buy

Tapentadol Hydrochloride Chemical Properties,Uses,Production

Description

Agonism of the MOR is a common strategy for moderate to severe pain intervention. Opioid drugs, such as morphine, that modulate this receptor have demonstrated efficacy in acute situations; however, chronic conditions, particularly those of neuropathic or inflammatory etiology, suffer from inadequate pain management with this treatment. With a narrow therapeutic window, traditional MOR agonists flirt with side effects at optimal analgesia, and prolonged use increases the potential for physical dependency. Since extensive efforts to design activators of MOR have failed to dissociate the undesirable adverse effects from the analgesic properties, the focus has been on enhancing the analgesic efficacy through a dual mechanism of action. Tapentadol hydrochloride brings this concept to fruition; MOR agonism is coupled with noradrenaline reuptake inhibition in a combinatory contribution to analgesia. Compared to morphine, it is about 50-fold less potent for MOR (Ki = 100 nM for tapentadol versus 2 nM for morphine). The Ki for inhibition of noradrenaline reuptake was 500 nM while reuptake of serotonin was only weakly inhibited (Ki = 2.5μM). Despite its lower affinity for MOR, the dual mechanism has provided an efficacious profile in both acute and chronic conditions with fewer side effects.

Chemical Properties

Light Brown Solid

Originator

Grunenthal GmbH (Germany)

Uses

A novel, centrally acting oral analgesic with a dual mode of action that has demonstrated efficacy in preclinical and clinical models of pain relief.

brand name

Nucynta

Clinical Use

Tapentadol was approved by the FDA in November 2008 for the treatment of moderate to severe acute pain. It is a centrally acting analgesic that acts as both an agonist at the l-opiod receptor and as a norepinephrine re-uptake inhibitor, allowing it to have efficacy similar to potent narcotic analgesics but without their side effects. The drug was developed by Grunenthal and Johnson & Johnson and was marketed starting in 2009.

Side effects

The common adverse effects of tapentadol were nausea, vomiting, somnolence, dizziness, and itching. As with all opioid medications, constipation was also an issue. Tapentadol is contraindicated in patients taking monoamine oxidase inhibitors because of the potential for adverse cardiovascular events due to additive effects on norepinephrine levels. As with other MOR agonists, it is also contraindicated in patients with paralytic ileus. In patients with a history of epilepsy or seizure, tapentadol may induce seizures. Since tapentadol causes somnolence, its combination with other sleep aids could dangerously affect breathing. Similarly, patients with existing breathing or lung problems are cautioned about using tapentadol. Furthermore, patients with past or present substance abuse or drug addiction should consult the doctor prior to use since physical dependency and addiction is a risk with tapentadol. Alcohol should be avoided due to the potential additive effect on CNS depression.

Synthesis

The synthesis of tapentadol hydrochloride begins with diethyl ketone, which is subjected to a standard Mannich condition to provide a b-dimethylamino intermediate. A Grignard reaction with 3-bromoanisole was followed by the separation of diastereomers and racemic resolution. Treatment with thionyl chloride converts the hydroxy group to its corresponding chloride, which is removed by treatment with zinc borohydride (generated from zinc chloride and sodium borohydride), with overall retention of stereochemistry. The methyl ether is cleaved in refluxing HBr to afford the tapentadol salt that is ultimately converted to the hydrochloride for formulation into 50-, 75-, and 100-mg immediate-release (IR) oral tablets.

Drug interactions

Potentially hazardous interactions with other drugs Analgesics: possible opioid withdrawal with buprenorphine and pentazocine.
Antidepressants: possible CNS excitation or depression with MAOIs - avoid concomitant use, and for 2 weeks after stopping MAOI; possible CNS excitation or depression with moclobemide; increased sedative effects with tricyclics.
Antihistamines: increased sedative effects with sedating antihistamines.
Antipsychotics: enhanced hypotensive and sedative effects.
Dopaminergics: avoid with selegiline.
Nalmefene: avoid concomitant use.
Sodium oxybate: enhanced effect of sodium oxybate - avoid concomitant use.

Metabolism

Approximately 97% of the parent compound is metabolised by conjugation with glucuronic acid to produce glucuronides. It is also metabolised, to a lesser extent, via the cytochrome P450 isoenzymes CYP2C9, CYP2C19, and CYP2D6, before further conjugation.
None of the metabolites have analgesic activity.
Approximately 70% of the dose is excreted in the urine in the conjugated form and 3% as unchanged drug.

Tapentadol Hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 93)Suppliers
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Nantong Guangyuan Chemicl Co,Ltd
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View Lastest Price from Tapentadol Hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Tapentadol Hydrochloride pictures 2024-03-08 Tapentadol Hydrochloride
175591-09-0
US $10.00 / kg 1kg 99% 1000kg Nantong Guangyuan Chemicl Co,Ltd
Tapentadol Hydrochloride pictures 2019-07-06 Tapentadol Hydrochloride
175591-09-0
US $2.00 / kg 1kg 99% 100kg Career Henan Chemical Co
3-[(1R,2R)-3-(Dimethylamino)-1-ethyl-2-methylpropyl]phenol Hydrochloride Tapentadol Hydrochloride Tapentadol hcl Phenol, 3-[(1R,2R)-3-(diMethylaMino)-1-ethyl-2-Methylpropyl]-, (HCl salt) 3-[(1R,2R)-3-(DiMethylaMino)-1-ethyl-2-Methylpro 3-((2R,3R)-1-(diMethylaMino)-2-Methylpentan-3-yl)phenol hydrochloride Phenol,3-[(1R,2R)-3-(diMethylaMino)-1-ethyl-2-Methylpropyl]-, hydrochloride (1:1) Tapentadol hydrochloride solution benzyl hydrogen (3-(((2R,3S)-2-((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy)-3-(4-fluorophenyl)morpholino)methyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)phosphonate Tapentadol (hydrochloride) (CRM) Tapentadol Hydrochloride (1.0 mg/mL in Methanol) Tapentediol Tapentadol hydrochloride(Y0002120) Tapentadol HydrochlorideQ: What is Tapentadol Hydrochloride Q: What is the CAS Number of Tapentadol Hydrochloride Q: What is the storage condition of Tapentadol Hydrochloride Q: What are the applications of Tapentadol Hydrochloride 175591-09-0 C14H23NOHCl C14H24ClNO Inhibitors Chiral Reagents Intermediates & Fine Chemicals Pharmaceuticals intermediate