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CAS RN: 68547-97-7 | Product Number: I0871
Isoguvacine Hydrochloride
Purity: >98.0%(HPLC)
Synonyms:
- 1,2,3,6-Tetrahydropyridine-4-carboxylic Acid Hydrochloride
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time | Shipping Information |
---|---|---|---|---|---|
25MG |
$108.00
|
17 | 4 | Contact Us |
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* The storage conditions are subject to change without notice.
Product Number | I0871 |
Purity / Analysis Method | >98.0%(HPLC) |
Molecular Formula / Molecular Weight | C__6H__9NO__2·HCl = 163.60 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Refrigerated (0-10°C) |
Condition to Avoid | Heat Sensitive |
Packaging and Container | 25MG-Glass Bottle with Plastic Insert (View image) |
CAS RN | 68547-97-7 |
Related CAS RN | 64603-90-3 |
Reaxys Registry Number | 5114285 |
PubChem Substance ID | 253660211 |
MDL Number | MFCD00055192 |
Specifications
Appearance | Light orange to Yellow to Green powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Properties (reference)
Melting Point | 280 °C(dec.) |
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
Precautionary Statements | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
Related Laws:
Transport Information:
H.S.code* | 2933.39-000 |
Application
Isoguvacine Hydrochloride: A γ-Aminobutyric Acid Subtype A (GABAA) Receptor Agonist
Isoguvacine hydrochloride is a γ-aminobutyric acid subtype A (GABAA) receptor agonist used in scientific research. As a reference, GABAA receptor is widely considered to be an important target for most clinically effective sedative-hypnotic compounds. (The product is for research purpose only.)
References
- A new class of GABA agonist
- Isoguvacine binding, uptake, and release: relation to the GABA system
- Spinal GABAA and GABAB receptor pharmacology in a rat model of neuropathic pain
- GABA(A) receptor ligands and their therapeutic potentials (a review)
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