Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Acrivastine

Base Information Edit
  • Chemical Name:Acrivastine
  • CAS No.:87848-99-5
  • Molecular Formula:C22H24N2O2
  • Molecular Weight:348.445
  • Hs Code.:
  • European Community (EC) Number:618-080-6
  • UNII:A20F9XAI7W
  • DSSTox Substance ID:DTXSID6022555
  • Nikkaji Number:J22.097C
  • Wikipedia:Acrivastine
  • Wikidata:Q342745
  • NCI Thesaurus Code:C47383
  • Pharos Ligand ID:Y4NMM72T56MQ
  • Metabolomics Workbench ID:152403
  • ChEMBL ID:CHEMBL1224
  • Mol file:87848-99-5.mol
Acrivastine

Synonyms:acrivastine;BW 825C;BW-825C;BW825C;Semprex

Suppliers and Price of Acrivastine
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Acrivastine
  • 250mg
  • $ 585.00
  • Sigma-Aldrich
  • Acrivastine ≥98% (HPLC)
  • 10mg
  • $ 69.90
  • Sigma-Aldrich
  • Acrivastine ≥98% (HPLC)
  • 50mg
  • $ 272.00
  • Medical Isotopes, Inc.
  • Acrivastine
  • 25 mg
  • $ 1500.00
  • DC Chemicals
  • Acrivastine >98%
  • 1 g
  • $ 800.00
  • CSNpharm
  • Acrivastine
  • 50mg
  • $ 194.00
  • ChemScene
  • Acrivastine 99.37%
  • 100mg
  • $ 324.00
  • ChemScene
  • Acrivastine 99.37%
  • 50mg
  • $ 228.00
  • ChemScene
  • Acrivastine 99.37%
  • 10mg
  • $ 66.00
  • Cayman Chemical
  • Acrivastine ≥98%
  • 25mg
  • $ 140.00
Total 92 raw suppliers
Chemical Property of Acrivastine Edit
Chemical Property:
  • Vapor Pressure:3.72E-13mmHg at 25°C 
  • Melting Point:55.5-59.5°C(lit.) 
  • Refractive Index:1.627 
  • Boiling Point:555.1 °C at 760 mmHg 
  • PKA:1.99±0.10(Predicted) 
  • Flash Point:289.5 °C 
  • PSA:53.43000 
  • Density:1.17 g/cm3 
  • LogP:3.95320 
  • Storage Temp.:2-8°C 
  • Solubility.:DMSO: >2mg/mL (warmed) 
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:6
  • Exact Mass:348.183778013
  • Heavy Atom Count:26
  • Complexity:514
Purity/Quality:

99% *data from raw suppliers

Acrivastine *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xn,Xi 
  • Hazard Codes:Xn,Xi 
MSDS Files:

SDS file from LookChem

Useful:
  • Drug Classes:Antihistamines
  • Canonical SMILES:CC1=CC=C(C=C1)C(=CCN2CCCC2)C3=CC=CC(=N3)C=CC(=O)O
  • Isomeric SMILES:CC1=CC=C(C=C1)/C(=C\CN2CCCC2)/C3=CC=CC(=N3)/C=C/C(=O)O
  • Description Acrivastine is an orally-active HI .receptor antagonist reportedly useful in the treatment of allergic rhinitis. The main advantages of acrivastine in comparison to older antihistamines are its low sedative potential and the absence of anticholinergic side-effects. Acrivastine is a histamine H1 receptor antagonist with a Ki value of 10 nM in COS-7 cells expressing the human receptor. In vivo, acrivastine (1 mg/kg) completely inhibits response to histamine in guinea pigs. Formulations containing acrivastine have been used for the treatment of seasonal allergies and hay fever.
  • Uses Antihistaminic. Acrivastine has been used as an antihistamine to investigate the relation between the increased residence time of antihistamine at the histamine H1 receptor (H1R) and the duration of effective target-inhibition by this antagonist.
  • Therapeutic Function Antihistaminic
  • Clinical Use Acrivastine, an acidic congener of triprolidine in which a carboxylic acid–substituted chain has been attached, also is a second-generation, nonsedating antihistamine. Penetration of the blood-brain barrier is limited, and it is less sedating than triprolidine. It is used principally in a combination with a decongestant.
Technology Process of Acrivastine

There total 9 articles about Acrivastine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With silica gel; potassium hydroxide; In acetone; at 35 - 45 ℃; for 2h; Reagent/catalyst; Solvent; Temperature; Inert atmosphere; Green chemistry;
Guidance literature:
Multi-step reaction with 5 steps
1: 12.2 g / BuLi / hexane; diethyl ether / 3 h / -50 °C
2: 24.3 g / p-toluenesulfonic acid / toluene / 6 h / Heating
3: 2.5 g / BuLi / diethyl ether; hexane / 4 h / -50 °C
4: 1.) NaH, 2.) conc. HCl / 1.) DME, 2 h, 2.) ethanol, H2O, steam bath, 10 min
5: 1.) BuLi, 2.) NaOH / 1.) hexane, toluene, 75 deg C, 2 h, 2.) ethanol, steam bath, 10 min
With hydrogenchloride; sodium hydroxide; n-butyllithium; sodium hydride; toluene-4-sulfonic acid; In diethyl ether; hexane; toluene;
DOI:10.1002/jps.2600731003
Guidance literature:
Multi-step reaction with 4 steps
1: 24.3 g / p-toluenesulfonic acid / toluene / 6 h / Heating
2: 2.5 g / BuLi / diethyl ether; hexane / 4 h / -50 °C
3: 1.) NaH, 2.) conc. HCl / 1.) DME, 2 h, 2.) ethanol, H2O, steam bath, 10 min
4: 1.) BuLi, 2.) NaOH / 1.) hexane, toluene, 75 deg C, 2 h, 2.) ethanol, steam bath, 10 min
With hydrogenchloride; sodium hydroxide; n-butyllithium; sodium hydride; toluene-4-sulfonic acid; In diethyl ether; hexane; toluene;
DOI:10.1002/jps.2600731003
Post RFQ for Price