ChemicalBook > CAS DataBase List > Tenoxicam

Tenoxicam

Product Name
Tenoxicam
CAS No.
59804-37-4
Chemical Name
Tenoxicam
Synonyms
Lornoxicam Impurity 44;Soral;Liman;Do1men;Dolmen;Alganex;Tilatil;tilcotil;MOBIFLEX;Epicotil
CBNumber
CB2163299
Molecular Formula
C13H11N3O4S2
Formula Weight
337.37
MOL File
59804-37-4.mol
More
Less

Tenoxicam Property

Melting point:
209-2130C (dec)
Density 
1.4737 (rough estimate)
refractive index 
1.6390 (estimate)
storage temp. 
2-8°C
solubility 
Practically insoluble in water, sparingly soluble in methylene chloride, very slightly soluble in anhydrous ethanol. It dissolves in solutions of acids and alkalis.
pka
pKa1 5.3, pKa2 1.1(at 25℃)
form 
Solid
color 
White to Yellow to Green
Water Solubility 
61.9mg/L(32 ºC)
CAS DataBase Reference
59804-37-4
More
Less

Safety

Hazard Codes 
T,Xi
Risk Statements 
23/24/25-36/37/38
Safety Statements 
36/37/39-45-36-26-36/37
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
2
RTECS 
XJ9095060
HS Code 
2934.99.3000
HazardClass 
6.1
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
T0909
Product name
Tenoxicam
Purity
NSAID
Packaging
1g
Price
$288
Updated
2024/03/01
Sigma-Aldrich
Product number
BP709
Product name
Tenoxicam degradation impurity standard
Purity
British Pharmacopoeia (BP) Reference Standard
Packaging
25MG
Price
$266
Updated
2024/03/01
Sigma-Aldrich
Product number
BP708
Product name
Tenoxicam
Purity
British Pharmacopoeia (BP) Reference Standard
Packaging
100MG
Price
$223
Updated
2024/03/01
Sigma-Aldrich
Product number
T0909
Product name
Tenoxicam
Purity
NSAID
Packaging
5g
Price
$1000
Updated
2023/06/20
TCI Chemical
Product number
T2750
Product name
Tenoxicam
Packaging
5G
Price
$57
Updated
2024/03/01
More
Less

Tenoxicam Chemical Properties,Usage,Production

Description

Tenoxicam is a non-steroidal antiinflammatory agent with a profile similar to related piroxicam and now withdrawn isoxicam (55). It is useful in the treatment of rheumatoid arthritis, osteoarthritis and related disorders.

Chemical Properties

Yellow Crystalline Powder

Originator

Hoffmann-La Roche (Switzerland)

Uses

Tenoxicam has been used:
    as a non-steroidal anti-inflammatory agent (NSAID) to study its effects on root gravitropism in Arabidopsis thaliana
    as a standard in microanalysis of NSAIDs by spectrophotometry
    to test its effect on surface potential andmembrane fluidity modification in phosphoglyceride monolayers

Definition

ChEBI: Tenoxicam is a thienothiazine-derived monocarboxylic acid amide obtained by formal condensation of the carboxy group of 4-hydroxy-2-methylthieno[2,3-e][1,2]thiazine-3-carboxylic acid 1,1-dioxide with the amino group of 2-aminopyridine. Used for the treatment of pain and inflammation in osteoarthritis and rheumatoid arthritis. It is also indicated for short term treatment of acute musculoskeletal disorders including strains, sprains and other soft-tissue injuries. It has a role as a non-steroidal anti-inflammatory drug, a non-narcotic analgesic, an antipyretic and an EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor. It is a heteroaryl hydroxy compound, a monocarboxylic acid amide, a member of pyridines and a thienothiazine.

brand name

Tilcotil

Biochem/physiol Actions

Tenoxicam (TX) possesses antipyretic?and analgesic effects. It elicits radical scavenging activity and has the potential to treat enkylosing spondylitis, extra-articular diseases, acute gout, and rheumatic diseases. It is also effective in treating primary dysmenorrhea, postpartum uterine contraction pain, and post-operation backaches. TX is capable of inhibiting prostaglandin synthesis.

Clinical Use

NSAID and analgesic

Synthesis

The reaction of methyl 3-hydroxythiophene- 2-carboxylate with PCl5 in refluxing CCl4 gives 3-chlorothiophene-2-carboxylic acid, which by treatment with NaHSO3 and Cu in aqueous alkaline solution at 143 ?C in a pressure vessel is converted into 3- sulfothiophene-2-carboxylic acid. Its esterification with refluxing methanol affords methyl- 3-sulfothiophene-2-carboxylate, which by reaction with refluxing SOCl2 yields methyl- 3-chlorosulfonylthiophene-2-carboxylate. The following condensation with sarcosine ethyl ester in hot CHCl3 gives 3-(N-ethoxycarbonylmethyl- N-methylsulfamoyl)thiophene-2-carboxylate, which is cyclized by treatment with sodium methoxide in refluxing methanol affording 3-ethoxycarbonyl-4-hydroxy-2-methyl-2Hthieno--1,2-thiazine 1,1-dioxide. Finally this compound is condensed with 2-aminopyridine in refluxing toluene

Drug interactions

Potentially hazardous interactions with other drugs
ACE inhibitors and angiotensin-II antagonists: antagonism of hypotensive effect; increased risk of nephrotoxicity and hyperkalaemia.
Analgesics: avoid concomitant use of 2 or more NSAIDs, including aspirin (increased side effects); avoid with ketorolac (increased risk of side effects and haemorrhage).
Antibacterials: possibly increased risk of convulsions with quinolones.
Anticoagulants: effects of coumarins and phenindione enhanced; possibly increased risk of bleeding with heparins, dabigatran and edoxaban - avoid long term use with edoxaban.
Antidepressants: increased risk of bleeding with SSRIs and venlaflaxine.
Antidiabetic agents: effects of sulphonylureas enhanced.
Antiepileptics: possibly increased phenytoin concentration.
Antivirals: increased risk of haematological toxicity with zidovudine; concentration possibly increased by ritonavir.
Ciclosporin: may potentiate nephrotoxicity.
Cytotoxics: reduced excretion of methotrexate; increased risk of bleeding with erlotinib.
Diuretics: increased risk of nephrotoxicity; antagonism of diuretic effect; hyperkalaemia with potassium-sparing diuretics.
Lithium: excretion decreased.
Pentoxifylline: increased risk of bleeding.
Tacrolimus: increased risk of nephrotoxicity.

Metabolism

Metabolised in the liver via cytochrome P450 2C9 to several pharmacologically inactive metabolites (mainly 5'-hydroxy-tenoxicam).
Metabolites are excreted mainly in the urine; there is some biliary excretion of glucuronide conjugates of the metabolites.

Tenoxicam Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Tenoxicam Suppliers

LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
AdooQ BioScience, LLC
Tel
+1 (866) 930-6790
Fax
+1 (866) 333-9607
Email
info@adooq.com
Country
United States
ProdList
2782
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32161
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Cayman Chemical Company
Tel
--
Fax
--
Email
cayman@caymanchem.com
Country
United States
ProdList
6213
Advantage
81
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
MedChemExpress
Tel
--
Fax
--
Email
sales@medchemexpress.com
Country
United States
ProdList
6398
Advantage
58
SynQuest Laboratories, Inc.
Tel
--
Fax
--
Email
info@synquestlabs.com
Country
United States
ProdList
6871
Advantage
62
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6962
Advantage
56
AlliChem, LLC
Tel
--
Fax
--
Email
sales@allichemllc.com
Country
United States
ProdList
6516
Advantage
60
ACIC Fine Chemicals Inc.
Tel
--
Fax
--
Email
sales@acic.com
Country
United States
ProdList
492
Advantage
48
Beta Pharma, Inc.
Tel
--
Fax
--
Email
sales@betapharma.com
Country
United States
ProdList
6226
Advantage
60
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
2A PharmaChem USA
Tel
--
Fax
--
Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
APAC Pharmaceutical, LLC
Tel
--
Fax
--
Email
sales@apacpharma.com
Country
United States
ProdList
6322
Advantage
38
ChemPacific Corporation
Tel
--
Fax
--
Email
sales@chempacific.com
Country
United States
ProdList
6891
Advantage
51
LKT Laboratories, Inc.
Tel
--
Fax
--
Email
info@lktlabs.com
Country
United States
ProdList
2164
Advantage
64
QVENTAS INC.
Tel
--
Fax
--
Email
mike@qventas.com
Country
United States
ProdList
383
Advantage
47
American Custom Chemicals Corporation
Tel
--
Fax
--
Email
sales@acccorporation.com
Country
United States
ProdList
6820
Advantage
51
BOSCHE SCIENTIFIC, LLC
Tel
--
Fax
--
Email
Sales@BoscheSci.com
Country
United States
ProdList
6477
Advantage
55
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
More
Less

View Lastest Price from Tenoxicam manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Tenoxicam 59804-37-4
Price
US $0.00/KG
Min. Order
1KG
Purity
98%min
Supply Ability
30tons/month
Release date
2023-02-25
BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
Product
Tenoxicam 59804-37-4
Price
US $0.00/g
Min. Order
1g
Purity
More Than 99%
Supply Ability
50kg/Month
Release date
2024-09-29
Wuhan Senwayer Century Chemical Co.,Ltd
Product
Tenoxicam 59804-37-4
Price
US $405.00/KG
Min. Order
1KG
Purity
99% min
Supply Ability
20 TONS
Release date
2022-10-14

59804-37-4, TenoxicamRelated Search:


  • 4-Hydroxy-2-methyl-N-pyridin-2-yl-2H-thieno[2,3-e][1,2]thiazine-3-carboxamide 1,1-dioxide (Tenoxicam)
  • MOBIFLEX
  • tilcotil
  • 3-Chlorosulfonyl-2-thiophene carboxylic acid methy
  • Do1men
  • 4-Hydroxy-2-methyl-N-2-pyridinyl-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamidel,1-dioxide
  • 2H-Thieno(2,3-e)-1,2-thiazine-3-carboxamide, 4-hydroxy-2-methyl-N-2-pyridinyl-, 1,1-dioxide
  • 4-Hydroxy-2-methyl-N-2-pyrimidinyl-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide 1,1-dioxide
  • 4-Hydroxy-2-methyl-3-[(2-pyridyl)carbamoyl]-2H-thieno[2,3-e][1,2]thiazine 1,1-dioxide
  • 4-Hydroxy-2-methyl-N-(2-pyridyl)-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide 1,1-bisoxide
  • 4-Hydroxy-2-methyl-N-(2-pyridyl)-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide 1,1-dioxide
  • Epicotil
  • OxaMen-L
  • Soral
  • TenoxicaM API
  • 4-hydroxy-2-Methyl-1,1-dioxo-N-(pyridin-2-yl)-2H-1$l^{6},5,2-thieno[2,3-e][1$l^{6},2]thiazine-3-carboxaMide
  • Tenoxicam Solution, 100ppm
  • 1,1-dioxide-4-hydroxy-2-methyl-N-2-pyridinyl-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide
  • TENOXICAM
  • 4-HYDROXY-2-METHYL-N-2-PYRIDINYL-2H-THIENO[2,3-E]-1,2-THIAZINE-3-CARBOXAMIDE 1,1-DIOXIDE
  • AKOS 93347
  • 3-e)-1,2-thiazine-3-carboxamide,4-hydroxy-2-methyl-n-2-pyridinyl-2h-thieno(
  • 4-hydroxy-2-methyl-n-2-pyridinyl-2h-thieno(2,3-e)-1,2-thiazine-3-carboxamide
  • ro12-0068
  • TENATOPRAZOLESODIUM
  • 4-Hydroxy-2-(methyl-d3)-N-(2-pyridyl)-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide 1,1-dioxide
  • Tenoxicam-(methyl-d3)
  • Tenoxicam (Mobiflex)
  • 4-Hydroxy-2-methyl-N-pyridin-2-yl-2H-thieno[2,3-e][1,2]thiazine-3-carboxamide-1,1-dioxide
  • TENOXICAM ASSAY STANDARD BP(CRM STANDARD)
  • TENOXICAM BP STANDARD(CRM STANDARD)
  • TENOXICAM EPT(CRM STANDARD)
  • TenoxicamBp98
  • Alganex
  • Dolmen
  • Liman
  • Rexalgan
  • Tilatil
  • 2H-Thieno(2,3-e)-1,2-thiyzin-3-carboxamid, 4-hydroxy-2-methyl-N-2-pyridinyl-, 1,1-dioxid
  • 69804-37-4
  • Tenoxicam CRS
  • Tenoxicamum
  • enoxicam
  • Tenoxicam USP/EP/BP
  • Lornoxicam Impurity 44
  • Mobiflex, Tenoxicam
  • 6-chloro-4-hydroxy-2-methyl-2H-thieno[2,3-e][1,2]thiazine-3- carboxamide 1,1-dioxide
  • Deschloro analog of lornoxicam/tenoxicam
  • C17235000 Tenoxicam
  • 59804-37-4
  • 156-2-32
  • 69804-37-4
  • 9804-37-4
  • C13H11N3O4S2
  • BioChemical
  • Biochemicals and Reagents
  • Enzyme Inhibitors
  • Enzyme Inhibitors by Type