ChemicalBook > CAS DataBase List > Desloratadine

Desloratadine

Product Name
Desloratadine
CAS No.
100643-71-8
Chemical Name
Desloratadine
Synonyms
DESLORATIDINE;Clarinex;Desloratadine Citrate Disodium;descarboethoxyloratadine;Loratadine Related Compound A (15 mg) (8-chloro-6,11-dihydro-11(4-piperidylidene)-5H-benzo[5,6]cyclohepta[1,2-b] pyridine);DesL;Allex;AzoMyr;Opulis;Aerius
CBNumber
CB3462564
Molecular Formula
C19H19ClN2
Formula Weight
310.82
MOL File
100643-71-8.mol
More
Less

Desloratadine Property

Melting point:
150-151°C
Boiling point:
467.9±45.0 °C(Predicted)
Density 
1?+-.0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
DMSO: >10mg/mL
pka
10.27±0.20(Predicted)
form 
powder
color 
White to Light orange to Yellow
Merck 
14,2922
BCS Class
1
InChIKey
JAUOIFJMECXRGI-UHFFFAOYSA-N
CAS DataBase Reference
100643-71-8(CAS DataBase Reference)
More
Less

Safety

WGK Germany 
3
RTECS 
DE8011000
HS Code 
2933399090
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H302Harmful if swallowed

H318Causes serious eye damage

H361Suspected of damaging fertility or the unborn child

H411Toxic to aquatic life with long lasting effects

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

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

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

P281Use personal protective equipment as required.

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

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P308+P313IF exposed or concerned: Get medical advice/attention.

P310Immediately call a POISON CENTER or doctor/physician.

P330Rinse mouth.

P405Store locked up.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
1370280
Product name
Loratadine Related Compound A
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
15mg
Price
$1380
Updated
2024/03/01
Sigma-Aldrich
Product number
1173042
Product name
Desloratadine
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
200mg
Price
$436
Updated
2024/03/01
TCI Chemical
Product number
D3787
Product name
Desloratadine
Purity
>98.0%(HPLC)(T)
Packaging
100mg
Price
$34
Updated
2024/03/01
TCI Chemical
Product number
D3787
Product name
Desloratadine
Purity
>98.0%(HPLC)(T)
Packaging
1g
Price
$200
Updated
2024/03/01
Cayman Chemical
Product number
16931
Product name
Desloratadine
Purity
≥98%
Packaging
50mg
Price
$49
Updated
2024/03/01
More
Less

Desloratadine Chemical Properties,Usage,Production

Description

Desloratadine is a second generation of tricyclic antihistamine. It is a H1-receptor antagonist which has anti-inflammatory activity. Its affinity to the H1 receptor is higher than most other H1-receptor antagonists. Desloratadine works by blocking a certain natural substance (histamine) which is produced during an allergic reaction. Desloratidine has a long-lasting effect and does not cause drowsiness because it does not readily enter the central nervous system.
Desloratadine is used to treat nasal and non-nasal symptoms (watery eyes, runny nose, itching eyes/nose, sneezing, and itching) of seasonal allergic rhinitis. It is also used to relieve chronic itching caused by hives.

Chemical Properties

Beige Solid

Originator

Sepracor (US)

Uses

Desloratadine has been used to test its effect on embryoid body development in in vitro gastrulation model of P19C5 stem cells. It has also been used as an antihistamine mimic in rats and to treat lung cancer (A549) and glioblastoma (U87) cells in various cellular studies.

Uses

Nonsedating-type histamine H1-receptor antagonist. An active metabolite of Loratadine. Also inhibits generation and release of inflammatory mediators from basophils and mast cells.

Uses

antiinflammatory

Uses

For the relief of symptoms of seasonal allergic rhinitis, perennial (non-seasonal) allergic rhinitis. Desloratidine is also used for the sympomatic treatment of pruritus and urticaria (hives) associated with chronic idiopathic urticaria.

Definition

ChEBI: Loratadine in which the ethoxycarbonyl group attached to the piperidine ring is replaced by hydrogen. The major metabolite of loratidine, desloratadine is an antihistamine which is used for the symptomatic relief of allergic conditions including rhinitis nd chronic urticaria. It does not readily enter the central nervous system, so does not cause drowsiness.

Indications

Desloratadine (Clarinex) is an active metabolite of loratadine. A 5 mg daily dose has been shown to be effective. There is no evidence that it offers any advantage over loratadine. Fexofenadine (like its parent compound terfenadine) may rarely promote cardiac arrhythmias (24). No significant difference in efficacy has been noted in the nonsedating H1 blockers. Combinations of nonsedating antihistamines in the morning and sedating antihistamines in the evening may be more cost effective than increasing doses of the nonsedating agent.

Manufacturing Process

To a solution of 10.9 g (0.1 mole) of ethylchloroformate in 300 ml of anhydrous benzene is added dropwise, with stirring at room temperature, a solution of 16.2 g (0.05 M) of 11-(N-methyl-4-piperidylidene)-8-chloro-6,11- dihydro-5H-benzo-[5,6]-cyclohepta-[1,2-b]-pyridine in 200 ml of benzene. The solution is stirred and is heated under reflux overnight (16-20 hours). The mixture is cooled and is poured into ice water and the organic layer is separated, washed with water, dried, and then concentrated to dryness. The residue is triturated with petroleum ether and a white solid of 8-chloro-6,11- dihydro-11-(1-ethoxycarbonyl-4-piperidylidene)-5H-benzo[5,6 ]cyclohepta[1,2-b]pyridine having a melting point of 128-130°C is recrystallized from isopropyl ether after decolorization with decolorizing carbon.
To 12 g of sodium hydroxide in 30 ml ethyl alcohol (70%) add 6 g of 8-chloro6,11-dihydro-11-(1-ethoxycarbonyl-4-piperidylidene)-5Hbenzo[5,6]cyclohepta[1,2-b]pyridine and reflux with stirring for 24 hours. After about the first 6-8 hours an additional 30 ml of 70% ethyl alcohol may be added. Remove about 50% of the solvent by distillation in vacuo. Add a small amount of ice water and acidify with glacial acetic acid. Extract with chloroform (6-8 times), since the product precipitates from the acetic acid solution as a thick emulsion which cannot be filtered. Concentrate the chloroform extracts to a small volume and precipitate the product with hexane to give crude 8-chloro-6,11-dihydro-11-(4-piperidylidene)-5Hbenzo[5,6]cyclohepta[1,2-b]pyridine acetic acid salt, m.p. 197-200°C. Recrystallize from benzene-hexane to obtain the product, m.p. 199-200°C. Yield 4.0-4.5 g.

brand name

Clarinex (Schering-Plough).

Therapeutic Function

Antiallergic

General Description

Desloratadine, 8-chloro-6,11-dihydro-11-(4-piperdinylidene)-5H-benzo[5,6]cyclohepta[1,2-b]pyridine(Clarinex) is a white to off-white powder that is slightlysoluble in water, but very soluble in ethanol and propyleneglycol. It is the proposed active metabolite loratadine and hasa very similar receptor binding and safety profile. It is indicated for the symptomatic relief of pruritus andreduction in the number and size of hives in chronic idiopathicurticaria patients 6 months of age and older and for therelief of the nasal and nonnasal symptoms of perennial allergicrhinitis (in patients 6 months of age and older) and seasonalallergic rhinitis (in patients 2 years of age and older).
Desloratadine is extensively metabolized to 3-hydroxydesloratadine,also an active metabolite, which is subsequentlyglucuronidated . The cytochrome enzymesresponsible for the formation of 3-hydroxydesloratadinehave not been reported. Coadministration ofdesloratadine with CYP3A4 inhibitors results in marginalincreases in plasma concentrations of desloratadine and3-hydroxydesloratadine, but no significant changes in safetyor efficacy. The mean elimination half-life of desloratadineis about 6 hours, and the drug and its metabolites areeliminated in the urine and feces.

Biochem/physiol Actions

Desloratadine is a selective and nonsedating histamine H1 receptor antagonist, an active metabolite of loratadine (Claritin), used to relieve hay fever and allergy symptoms with less drowsiness than other antihistamines; does not significantly inhibits cardiac K+ channels at clinically achievable blood levels. Free from antimuscarinic/anticholinergic effects.

Clinical Use

Desloratadine was launched as an improved version of Schering-Plough's Claritin? (Loratadine), for the treatment of nasal and non-nasal symptoms of seasonal allergic rhinitis (SAR). Desloratadine can be prepared by a 7-step synthesis starting with a Ritter reaction on 2-cyano-3-picoline and involving successively alkylation with 3- chlorobenzyl chloride, dehydration, Grignard reaction with the piperidine magnesium chloride, intramolecular cyclization in strong acidic medium, and finally demethylation of the piperidine. Desloratadine (the descarboethoxyloratadine) is a biologically active metabolite of the second-generation antihistamine Ioratadine. Desloratadine is a nonsedating competitive histamine H1 receptor antagonist with increased potency and improved safety as compared to Ioratadine. When compared with other H1 antagonists as an inhibitor of histamine-induced calcium flux in CHO cells, desloratadine was found to be more potent than most H1 antagonists (such as the widely used terfenadine, fexofenadine, cetirizine, Ioratadine and astemizole) in this assay. Desloratadine is also a potent antagonist of muscarinic M1 and M3 receptors (not M2) indicating anticholinergic activity. These effects may be the explanation for the unexpected decongestant effects of desloratadine reported in clinical trials. Desloratadine appears to be devoid of significant effects on potassium channels and does not appear to suffer from adverse interaction with cytochrome P450 inhibitors. Clinical studies have shown that it does not induce sedation or cardiac arrhythmias and does not potentiate the effects of alcohol. Apparent total body clearance is in the range of 114-201 l/h and the mean elimination half life is 19-34.6 h in human. Desloratadine is available as 5-mg tablets, which is the once-daily recommended dose for adults and children above 12 years. It may be taken without regard to food. The treatment not only improved symptoms of SAR but also improved patient ratings of nasal congestion. The FDA also has issued an "approvable" letter for this agent for the treatment of chronic idiopathic urticaria (ClU).

References

[1] https://www.drugbank.ca
[2] Raif S. Geha, Eli O. Meltzer (2001) Desloratadine: A new, nonsedating, oral antihistamine, The Journal of Allergy and Clinical Immunology,107, 751-762

Desloratadine Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Desloratadine Suppliers

Americas 1 Argentina 2 Austria 1 Bangladesh 1 Brazil 2 Canada 6 China 410 Colombia 1 Europe 3 France 4 Germany 9 Greece 1 India 165 Indonesia 1 Israel 2 Italy 1 Japan 1 Jordan 1 Malaysia 1 Mexico 1 Nepal 1 Slovenia 1 South Korea 2 Spain 2 Switzerland 3 United Arab Emirates 2 United Kingdom 19 United States 56 Uruguay 1 Global 701
Jai Radhe Sales
Tel
+(91)-(79)-26431096/65255722
Fax
+(91)-(79)-26569884
Email
info@jairadhesales.com
Country
India
ProdList
397
Advantage
60
TCI Chemicals (India) Pvt. Ltd.
Tel
--
Fax
--
Email
sales-in@tcichemicals.com
Country
India
ProdList
6768
Advantage
58
Manus Aktteva
Tel
--
Fax
--
Email
info@manusaktteva.in
Country
India
ProdList
581
Advantage
34
SL Drugs and Pharmaceuticals Pvt. Ltd.
Tel
--
Fax
--
Email
enquiry@sldrugs.com
Country
India
ProdList
2683
Advantage
50
VASUDHA PHARMA CHEM LIMITED
Tel
--
Fax
--
Email
vasudha@vasudhapharma.com
Country
India
ProdList
76
Advantage
58
Chemicea Pharmaceuticals Pvt Ltd
Tel
--
Fax
--
Email
sales@chemicea.com
Country
India
ProdList
825
Advantage
58
Unnati Pharmaceuticals Pvt. Ltd.
Tel
--
Fax
--
Email
unnatipharma@gmail.com
Country
India
ProdList
86
Advantage
58
Dharmanandan Export Pvt., Ltd.
Tel
--
Fax
--
Email
info@dnexport.com
Country
India
ProdList
161
Advantage
58
Abhilasha Pharma Pvt., Ltd.
Tel
--
Fax
--
Email
info@abhilashapharma.com
Country
India
ProdList
12
Advantage
58
Anamayee Pharmachem Pvt. Ltd
Tel
--
Fax
--
Country
India
ProdList
4
Advantage
58
Innorex Pharmaceuticals Private Limited
Tel
--
Fax
--
Email
info@innorexpharma.com
Country
India
ProdList
173
Advantage
58
Indogulf Group
Tel
--
Fax
--
Email
info@indogulfgroup.com
Country
India
ProdList
249
Advantage
58
Anant Pharmaceuticals Pvt. ltd
Tel
--
Fax
--
Email
info@anantlabs.com
Country
India
ProdList
736
Advantage
58
SL Drugs & Pharmaceuticals
Tel
--
Fax
--
Country
India
ProdList
72
Advantage
58
Anant Pharmaceuticals Pvt., Ltd.
Tel
--
Fax
--
Email
sales@anantlabs.com
Country
India
ProdList
160
Advantage
58
Aara Exim Private Limited
Tel
--
Fax
--
Country
India
ProdList
5
Advantage
58
Suvan LifeSciences (formerly Sansh Biotech Pvt., Ltd.)
Tel
--
Fax
--
Email
rahul@suvanlifesciences.com
Country
India
ProdList
38
Advantage
58
Synthink Research Chemicals
Tel
--
Fax
--
Country
India
ProdList
398
Advantage
58
Anzen Exports
Tel
--
Fax
--
Email
info@anzen.co.in
Country
India
ProdList
164
Advantage
58
Abhilasha Pharma Private Limited
Tel
--
Fax
--
Country
India
ProdList
2
Advantage
58
Aril Pharmaceuticals (Aril Biosciences Pvt. Ltd.)
Tel
--
Fax
--
Email
marketing@arilpharmaceuticals.com
Country
India
ProdList
67
Advantage
58
Vercali Pharma
Tel
--
Fax
--
Email
info@vercalipharma.com
Country
India
ProdList
13
Advantage
58
Ralington Pharma.
Tel
--
Fax
--
Email
info@ralingtonpharma.com
Country
India
ProdList
311
Advantage
58
Dolphin Chem
Tel
--
Fax
--
Country
India
ProdList
4
Advantage
58
Clearsynth Labs
Tel
--
Fax
--
Email
fo@clearsynth.com
Country
India
ProdList
3887
Advantage
58
Opulent Pharma
Tel
--
Fax
--
Country
India
ProdList
810
Advantage
58
Sris Pharmaceuticals
Tel
--
Fax
--
Email
marketing@srispharma.co.in
Country
India
ProdList
130
Advantage
58
Oceanic Pharmachem Pvt. Ltd.
Tel
--
Fax
--
Email
info@oceanicpharmachem.com
Country
India
ProdList
2005
Advantage
58
ENALTEC LABS PRIVATE LTD
Tel
--
Fax
--
Email
info@enaltec.com
Country
India
ProdList
27
Advantage
58
International Drug & Chemical Co.
Tel
--
Fax
--
Email
sales@idcco.com
Country
India
ProdList
65
Advantage
58
Gliesse Pharmaceuticals Pvt., Ltd.
Tel
--
Fax
--
Email
info@gliessepharma.com
Country
India
ProdList
165
Advantage
58
Pharmaffiliates Analytics & Synthetics (P) Ltd.
Tel
--
Fax
--
Email
g@pharmaffiliates.com
Country
India
ProdList
631
Advantage
58
Auracare Pharma Private Limited
Tel
--
Fax
--
Email
vinay@auracarepharma.com
Country
India
ProdList
55
Advantage
58
Pharma Affiliates
Tel
--
Fax
--
Email
@pharmaffiliates.com
Country
India
ProdList
6754
Advantage
58
Amsal Chem Private Limited
Tel
--
Fax
--
Country
India
ProdList
6
Advantage
58
Sun Pharmaceutical Industries Ltd.
Tel
--
Fax
--
Email
SunPharma.IndiaBusiness@sunpharma.com
Country
India
ProdList
99
Advantage
58
Amsal Chem Private Limited.
Tel
--
Fax
--
Email
sales@amsal.com
Country
India
ProdList
14
Advantage
58
Euro-India Chems Pvt., Ltd.
Tel
--
Fax
--
Email
euroindiachems@gmail.com
Country
India
ProdList
31
Advantage
58
Zeal Medipharma (Export) Private Limited.
Tel
--
Fax
--
Email
export3@zealmedipharmaexport.com
Country
India
ProdList
84
Advantage
58
Shree Raj Chem
Tel
--
Fax
--
Country
India
ProdList
91
Advantage
58
Novas International
Tel
--
Fax
--
Email
info@novasinternational.com
Country
India
ProdList
210
Advantage
58
Ken Pharma
Tel
--
Fax
--
Email
john@kenpharma.com
Country
India
ProdList
84
Advantage
58
Chromex Dyes
Tel
--
Fax
--
Country
India
ProdList
27
Advantage
58
Medilink Pharmachem
Tel
--
Fax
--
Email
info@medilinkpharma.com
Country
India
ProdList
58
Advantage
58
Cipla Ltd.
Tel
--
Fax
--
Email
exports@cipla.com
Country
India
ProdList
72
Advantage
58
Orient Pharma
Tel
--
Fax
--
Email
info@orientpharma.in
Country
India
ProdList
204
Advantage
58
J. B. Khokhani & Co.
Tel
--
Fax
--
Email
es@jbkhokhani.com
Country
India
ProdList
34
Advantage
58
Rawia International HealthCare Pvt. Ltd.
Tel
--
Fax
--
Email
info@rawia.in
Country
India
ProdList
170
Advantage
58
Athos Chemicals
Tel
--
Fax
--
Email
export@athoschemicals.com
Country
India
ProdList
315
Advantage
58
Gemini Exports
Tel
--
Fax
--
Email
uiry@geminiexpor
Country
India
ProdList
140
Advantage
58
More
Less

View Lastest Price from Desloratadine manufacturers

Moxin Chemicals
Product
Rupatadine EP Impurity B 100643-71-8
Price
US $0.00-0.00/mg
Min. Order
10mg
Purity
95%+
Supply Ability
10000
Release date
2025-01-22
Hebei Mujin Biotechnology Co.,Ltd
Product
Desloratadine 100643-71-8
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2024-10-11
Wuhan Haorong Biotechnology Co.,Ltd
Product
Desloratadine 100643-71-8
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
5000
Release date
2023-07-27

100643-71-8, DesloratadineRelated Search:

Loratadine 2,2,6,6-Tetramethyl-4-piperidinol Triacetonediamine DROPERIDOL Haloperidol Benzo[b]thien-2-ylboronic acid Cetirizine dihydrochloride Desloratadine IMpurity B Desloratadine Epoxide 8-Chloro-6,11-dihydro-11-(4-piperidinylidene)-5H-benzo[5,6]cyclohepta[1,2-b]pyridine-d 1-Oxide Desloratadine IMpurity 3 8-Chloro-11-fluoro-6,11-dihydro-11-(4-piperidinyl)-5H-benzo[5,6]cyclohepta[1,2-b]pyridine 8-Dechloro-9-chloro Desloratadine Desloratadine Citric Amide Desloratadine-d7 (Major) 8-Deschloro-8-bromo-N-methyl Desloratadine IMp. A (EP): Ethyl 4-[(11RS)-8-Chloro-11-hydroxy-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl]piperidine-1-carboxylate Desloratadine N-Carboxylic Acid Methyl Ester

  • AzoMyr
  • Neoclarityn
  • NSC 675447
  • Opulis
  • Desloratadine(Clarinex)
  • 5H-Benzo[5,6]cyclohepta[1,2-b]pyridine, 8-chloro-6,11-dihydro- 11-(4-piperidinylidene)-
  • Desloratadine for system suitability
  • Loratadine Related Compound A (15 mg) (8-chloro-6,11-dihydro-11(4-piperidylidene)-5H-benzo[5,6]cyclohepta[1,2-b] pyridine)
  • Clarinex (TN)
  • Clarinex RediTabs
  • Denosin
  • Desalex
  • Descarboethoxyoratidine
  • Desloratadine (USAN)
  • Desloratadine [USAN]
  • Loratadine EP IMpurity D
  • 8-chloro-11-piperidin-4-ylidene-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine
  • 8-Chloro-6,11-dihydro-11-(4-piperidylidene)-5H-benzo[5,6]cyclohepta[1,2-b] pyridine
  • Loratadine Impurity D (Desloratadine)(EP )
  • Loratadine EP Impurity D (Desloratadine) (Rupatadine EP Impurity B)
  • Rupatadine EP Impurity B (Loratadine EP Impurity D) (Desloratadine)
  • Loratadine Impurity 4(Loratadine EP Impurity D)
  • Loratadine EP Impurity D (Desloratadine)
  • 8-chloro-6,11-dihydro-11-(4-piperdinylidene)-5h-benzo[5,6]cyclohepta[1,2-b]pyridine
  • 8-CHLORO-6,11-DIHYDRO-11-(4-PIPERIDINYLIDENE)-5H-BENZO[5,6]CYCLOHEPTA[1,2-B]PYRIDINE
  • AKOS 92131
  • DESLORATIDINE
  • SCH-34117
  • Aerius
  • Dis-loratadine
  • Sch-34117, 8-Chloro-6,11-dihydro-11-(4-piperidinylidene)-5H- benzo[5,6]cyclohepta[1,2-b]pyridine, Clairinex, Aerius
  • descarboethoxyloratadine
  • Sch-34117, 8-Chloro-6,11-dihydro-11-(4-piperidinylidene)-5H- benzo[5,6]cyclohepta[1,2-β]pyridine, Clairinex, Aerius
  • Clarinex(R), 8-Chloro-6,11-dihydro-11-(4-piperidinylidene)-5H- benzo[5,6]cyclohepta[1,2,b]pyridine
  • Clarinex
  • Desloratadine Citrate Disodium
  • Loratadine Related CoMpound A
  • Loratadine Related Compound A (15 mg) (8-Chloro-6,11-dihydro-11(4-piperidinylidene)-5H-benzo[5,6]cyclohepta[1,2-b] pyridine)
  • 13-chloro-2-(piperidin-4-ylidene)-4-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3,5,7,11,13-hexaene
  • Allex
  • Rupatadine EP Impurity D
  • Loratadine Impurity D/ Rupatadine Impurity B
  • Rupatadine EP Impurity B
  • Loratadine impurity-D(EP)
  • DESLORATADINE IMPURITY-D, 8-CHLORO-6,11-DIHYDRO-11-(4-PIPERDINYLIDENE)- 5H-BENZO[5,6]CYCLOHEPTA[1,2-B]PYRIDINE.
  • Desloratadine&gt
  • Desloratadine for system suitability CRS
  • Desloratadine CRS
  • DesL
  • oratadine
  • esloratadine
  • Desloratadine USP/EP/BP
  • Desloratadine Citrate Disodium USP/EP/BP
  • Deslloratadine
  • Loratidine EP Impurity D/ Loratidine Related Compound A (Desloratadine)
  • desloratadine intermediate
  • 8-chloro-11-piperidin-4-ylidene-5,6-dihydrobenzo[1,2]cyclohepta[2,4-b]pyridine
  • Desloratadine (Sch34117)