Description References
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Ebastine

Description References
Product Name
Ebastine
CAS No.
90729-43-4
Chemical Name
Ebastine
Synonyms
EBASTIN;EBASTEL;LAS-90;Ebasine;Estivan;EVASTEL;KESTINE;ebastina;RP 64305;EBASTINE
CBNumber
CB8271800
Molecular Formula
C32H39NO2
Formula Weight
469.66
MOL File
90729-43-4.mol
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Ebastine Property

Melting point:
80-82°C
Boiling point:
596.3±50.0 °C(Predicted)
Density 
1.09±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
Slightly soluble in chloroform, methanol.
pka
8.19±0.10(Predicted)
form 
solid
color 
white
Merck 
14,3484
CAS DataBase Reference
90729-43-4(CAS DataBase Reference)
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Safety

WGK Germany 
3
RTECS 
EL8140000
HS Code 
2933.39.9200
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H303May be harmfulif swallowed

Precautionary statements

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P403Store in a well-ventilated place.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
E9531
Product name
Ebastine
Purity
≥98% (HPLC), solid
Packaging
10mg
Price
$257
Updated
2024/03/01
Sigma-Aldrich
Product number
E9531
Product name
Ebastine
Purity
≥98% (HPLC), solid
Packaging
50mg
Price
$853
Updated
2024/03/01
TCI Chemical
Product number
E0925
Product name
Ebastine
Purity
>98.0%(HPLC)(T)
Packaging
1g
Price
$144
Updated
2024/03/01
TCI Chemical
Product number
E0925
Product name
Ebastine
Purity
>98.0%(HPLC)(T)
Packaging
5g
Price
$494
Updated
2024/03/01
Alfa Aesar
Product number
J63088
Product name
Ebastine
Packaging
1g
Price
$146.65
Updated
2024/03/01
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Ebastine Chemical Properties,Usage,Production

Description

Ebastine belongs to an effective second generation histamine H1 receptor antagonist. One important property of it is that it doesn’t penetrate the blood brain barrier. Therefore, it is capable of blocking the H1 receptor in peripheral tissue without having some specific side effects such as sedation and drowsiness. Ebastine is mainly applied for the treatment of allergic rhinitis, pruritus as well as acting as an alternative drug in Decongestant. Upon entering into the human body, it can subject to the action of hepatic cytochrome P450 3A4 to be converted to an active carboxylic acid metabolite, carebastine. The later one is the major active form in vivo. Under certain range, it can inhibit T cell proliferation and the production of Th2-type pro-inflammatory cytokines through macrophages. Ebastine generally has a high safety property without causing cognitive/psychomotor impairment and sedation, like placebo. However, it can cause side effects such as inflammation of the air-cavities around nose, sore throat, indigestion, nausea, headache, and abdominal pain.

References

https://pubchem.ncbi.nlm.nih.gov/compound/3191#section=Top
http://www.tabletwise.com/medicine/ebastine/side-effects
http://www.druginfosys.com/drug.aspx?drugcode=897&type=1

Description

Ebastine is a new once-daily histamine Hl-receptor antagonist with no sedative effects or autonomic impairment at therapeutic doses. It is reported to be effective in the treatment of hay fever, perennial rhinitis, and uticaria. Ebastine's antihistamine activity is attributed to its carboxylic acid metabolite carebastine.

Chemical Properties

White to Off-White Powder

Originator

Almirall (Spain)

Uses

Ebastine is a second-generation H1 receptor antagonist that is indicated mainly for allergic rhinitis and chronic idiopathic urticaria. It is available in 10 and 20 mg tablets and as fast-dissolving tablets, as well as in pediatric syrup. It has a recommended flexible daily dose of 10 or 20 mg, depending on disease severity.

Uses

A nonsedating type histamine H1-receptor antagonist. Antihistaminic

Definition

ChEBI: Ebastine is an organic molecular entity.

Manufacturing Process

(a) A mixture of 4-hydroxypiperidine (40.4 g; 0.4 moles), p-tert-butyl-ω- chlorobutyrophenone (105 g, 0.44 moles), sodium bicarbonate (67.2 g; 0.8 moles) and a crystal of potassium iodide in methyl isobutyl ketone (1 liter) was boiled under reflux for 24 hours. After cooling, the reaction mixture waswashed with water, dried (Na2SO4) and the solvent removed in vacuum. The residue was salified with the stoichiometric amount of fumaric acid in a mixture of acetone and ethanol to give 1-[3-(4-tert-butylbenzoyl)propyl]-4- hydroxypiperidine fumarate (148 g), melting point 163-165°C. This compound was converted into the free base, and 1-[3-(4-tert-butylbenzoyl)propyl]-4- hydroxypiperidine was obtained and recrystallized from a mixture of diethyl ether and petroleum ether (boiling point 50-70°C). 102 g were obtained (yield 84%), melting point 63-65°C.
(b) A mixture of 1-[3-(tert-butylbenzoyl)propyl]-4-hydroxypiperidine (60.68 g; 0.2 moles) and sodium carbonate (42.4 g; 0.4 moles) in methyl isobutyl ketone (500 ml) was heated to the boiling point and a solution of diphenylmethyl bromide (49.42 g; 0.2 moles) in methyl isobutyl ketone (75 ml) was slowly added in 1.5 hours. The resulting mixture was boiled under reflux for another 12 hours, and then another solution of diphenylmethyl bromide (24.71 g; 0.1 moles) in methyl isobutyl ketone (50 ml) was added and the mixture boiled under reflux again for 12 hours. Another solution of diphenylmethyl bromide in the same quantity was added and after refluxing for 12 additional hours the reaction mixture was cooled, washed with water, dried (Na2SO4) and the solvent removed in vacuum.
The residual oil was treated with the stoichiometric amount of fumaric acid in ethanol and 4-diphenylmethoxy-1-[3-(4-tert-butylbenzoyl)propyl]piperidine fumarate crystallized. After recrystallisation from ethanol the pure compound was obtained (88 g; yield 75%), melting point 197-198°C.

brand name

Kestine (Rhone-Poulenc Rorer);Ebastel.

Therapeutic Function

Antihistaminic, Antiallergic, Calcium entry blocker

General Description

Ebastine is metabolised by cytochrome P450 3A (CYP3A4) to carebastine. It is used to treat allergic rhinitis and chronic idiopathic urticaria.

Biochem/physiol Actions

Ebastine is a non-sedating histamine H1 receptor antagonist, which inhibits allergen-induced bronchospasm in conscious guinea pigs. Unlike other compounds in this category, ebastine does not prolong the QT interval at up to five times the recommended therapeutic dose.

Ebastine Preparation Products And Raw materials

Raw materials

Preparation Products

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Ebastine Suppliers

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View Lastest Price from Ebastine manufacturers

Shanghai Affida new material science and technology center
Product
Ebastine 90729-43-4
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99
Supply Ability
20tons
Release date
2024-03-15
Shaanxi Dideu Medichem Co. Ltd
Product
Ebastine 90729-43-4
Price
US $1.00-1.00/KG
Min. Order
1g
Purity
99%
Supply Ability
50tons
Release date
2020-05-08
Hebei Yanxi Chemical Co., Ltd.
Product
Ebastine 90729-43-4
Price
US $0.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
20tons
Release date
2023-10-12

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