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CAS RN: 87848-99-5 | Product Number: A2764
Acrivastine
×
Purity: >98.0%(HPLC)
Synonyms:
Product Documents:
| Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time |
Shipping Information
|
|---|---|---|---|---|---|
| 20MG |
$47.00
|
22 | 0 | Contact Us | |
| 100MG |
$156.00
|
9 | 2 | Contact Us |
* Please contact our distributors or
TCI
to order our products. The above prices do not include freight cost, customs, and other charges to the destination.
* The storage conditions are subject to change without notice.
| Product Number | A2764 |
Purity / Analysis Method 
|
>98.0%(HPLC) |
| Molecular Formula / Molecular Weight | C__2__2H__2__4N__2O__2 = 348.45 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature
|
Refrigerated (0-10°C) |
| Condition to Avoid | Heat Sensitive |
| Packaging and Container
|
100MG-Glass Bottle with Plastic Insert (View image), 20MG-Glass Bottle with Plastic Insert (View image) |
| CAS RN | 87848-99-5 |
| Reaxys Registry Number | 6739893 |
| Merck Index (14) | 127 |
| MDL Number | MFCD00869830 |
Specifications
| Appearance | White to Almost white powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Elemental analysis(Nitrogen) | 7.50 to 8.50 % |
| NMR | confirm to structure |
Properties (reference)
| Melting Point | 215 °C(dec.) |
GHS
| Hazard Statements | H413 : May cause long lasting harmful effects to aquatic life. |
| Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P273 : Avoid release to the environment. |
Related Laws:
| RTECS# | UD3474000 |
Transport Information:
| H.S.code* | 2933.39-000 |
Application
Acrivastine: A Short Acting Histamine H1-Receptor Antagonist
Acrivastine is a short acting histamine H1-receptor antagonist. It has been reported that acrivastine have a short terminal elimination half-life [1.7-h] and an 8-h duration of action in humans. (The product is for research purpose only.)
References
- The acute effects of acrivastine (BW825C), a new antihistamine, compared with triprolidine on measures of central nervous system performance and subjective effects
- Clinical pharmacology of new histamine H1 receptor antagonists (a review)
- Delineation of receptor-ligand interactions at the human histamine H1 receptor by a combined approach of site-directed mutagenesis and computational techniques - or - how to bind the H1 receptor
- Simultaneous analysis of the H1-antihistamine acrivastine and the decongestant pseudoephedrine hydrochloride by high-performance liquid chromatography
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