MUSCIMOL
- CAS No.
- 2763-96-4
- Chemical Name:
- MUSCIMOL
- Synonyms
- AGARIN;MUSCIMOL;pantherin;NSC 333569;PANTHERINE;MUSCIMOL(P);Muscimol-RM;MUSCIMOL (RG);Muscimol (CRM);Pyroibotenic acid
- CBNumber:
- CB6231349
- Molecular Formula:
- C4H6N2O2
- Molecular Weight:
- 114.1
- MDL Number:
- MFCD00057894
- MOL File:
- 2763-96-4.mol
- MSDS File:
- SDS
- TDS File:
- TDS
| Melting point | 175-176°C |
|---|---|
| Boiling point | 213.59°C (rough estimate) |
| Density | 1.291 |
| refractive index | 1.4487 (estimate) |
| storage temp. | 2-8°C |
| solubility | ethanol: 1 mg/mL |
| form | powder |
| pka | 12.19±0.40(Predicted) |
| color | white to off-white |
| Water Solubility | Soluble in water (10 mg/ml), methanol, ethanol, 0.05 M HCl (20 mg/ml), DMSO (sparingly soluble), DMF (sparingly soluble), and PBS (pH 7.2) (10 mg/ml). |
| Merck | 13,6336 |
| BRN | 1618960 |
| Stability | Hygroscopic, Store in Freezer at -20°C |
| InChI | 1S/C4H6N2O2/c5-2-3-1-4(7)6-8-3/h1H,2,5H2,(H,6,7) |
| InChIKey | ZJQHPWUVQPJPQT-UHFFFAOYSA-N |
| SMILES | [N+H3]Cc1[o]nc(c1)[O-] |
| FDA UNII | D5M179TY2E |
| EPA Substance Registry System | 5-(Aminomethyl)-3-isoxazolol (2763-96-4) |
| UNSPSC Code | 12352200 |
| NACRES | NA.77 |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS06 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Danger | |||||||||
| Hazard statements | H300-H336 | |||||||||
| Precautionary statements | P261-P264-P270-P271-P301+P310-P304+P340+P312 | |||||||||
| target organs | Central nervous system | |||||||||
| Hazard Codes | T | |||||||||
| Risk Statements | 25 | |||||||||
| Safety Statements | 22-36/37/39-45 | |||||||||
| RIDADR | UN 1544 6.1/PG 2 | |||||||||
| WGK Germany | 3 | |||||||||
| RTECS | NY3345000 | |||||||||
| F | 3-10 | |||||||||
| TSCA | TSCA listed | |||||||||
| HazardClass | 6.1(a) | |||||||||
| PackingGroup | II | |||||||||
| HS Code | 29349990 | |||||||||
| Storage Class | 6.1A - Combustible, acute toxic Cat. 1 and 2 very toxic hazardous materials |
|||||||||
| Hazard Classifications | Acute Tox. 2 Oral STOT SE 3 |
|||||||||
| Hazardous Substances Data | 2763-96-4(Hazardous Substances Data) | |||||||||
| Toxicity | LD50 in mice (mg/kg): 3.8 s.c., 2.5 i.p.; in rats (mg/kg): 4.5 i.v., 45 orally (Theobald) | |||||||||
| NFPA 704 |
|
MUSCIMOL price More Price(32)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich | M1523 | Muscimol powder | 2763-96-4 | 5mg | $173 | 2026-04-30 | Buy |
| Sigma-Aldrich | M1523 | Muscimol powder | 2763-96-4 | 10mg | $266 | 2026-04-30 | Buy |
| Sigma-Aldrich | 5.06044 | Muscimol - CAS 2763-96-4 - Calbiochem Muscimol is a constituent and psychoactive ingredient of the mushroom Amanita muscaria, that acts as a potent agonist of GABAA receptors. | 2763-96-4 | 1MG | $104 | 2026-04-30 | Buy |
| Cayman Chemical | 13667 | Muscimol ≥98% | 2763-96-4 | 5mg | $83 | 2026-04-30 | Buy |
| Cayman Chemical | 13667 | Muscimol ≥98% | 2763-96-4 | 10mg | $132 | 2026-04-30 | Buy |
MUSCIMOL Chemical Properties,Uses,Production
Description
The amino acid γ-
Chemical Properties
Tan Solid
Uses
A potent but toxic structural analogue of g-aminobutyric acid (GABA), with a zwitterionic structure that can cross the blood-brain barrier
Uses
As a molecular probe to study GABA receptors.
Definition
ChEBI: A member of the class of isoxazoles that is 1,2-oxazol-3(2H)-one substituted by an aminomethyl group at position 5. It has been isolated from mushrooms of the genus Amanita.
Synthesis Reference(s)
The Journal of Organic Chemistry, 48, p. 4307, 1983 DOI: 10.1021/jo00171a030
Synthetic Communications, 12, p. 1089, 1982 DOI: 10.1080/00397918208065973
General Description
Crystals. Formerly used as a sedative and an anti-emetic.
Reactivity Profile
MUSCIMOL is a ketone and an amine. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides
Health Hazard
MUSCIMOL is a natural constituent of amanita mushrooms and is extremely toxic. It is a potent central nervous system depressant, and is believed to be responsible for most of the nervous system effects that result from eating this mushroom. The lowest toxic dose in humans has been reported at 109 mg/kg.
Health Hazard
Muscimol is a toxic alkaloid of poisonousmushroom species, producing neurologicaction. It is a potent depressant of thecentral nervous system. The adverse healtheffects from its ingestion include sleep,hallucination, distorted perceptions, andvomiting.
LD50 value, oral (mice): 17 mg/kgLD50 value, intraperitoneal (mice): 2.5 mg/kg.
Fire Hazard
When heated to decomposition, MUSCIMOL emits toxic fumes of nitrogen oxides.
Biological Activity
Potent GABA A receptor agonist and partial GABA C receptor agonist. Inhibits memory retention and attenuates airway constriction in vivo .
Potential Exposure
Formerly used as a sedative and as anantiemetic; and for experimental laboratory purposes.
First aid
If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Speed in removing material from skinis of extreme importance. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions,including resuscitation mask) if breathing has stopped andCPR if heart action has stopped. Transfer promptly to amedical facility. When this chemical has been swallowed,get medical attention. Give large quantities of water andinduce vomiting. Do not make an unconscious personvomit.
storage
Room temperature
Purification Methods
Recrystallise muscimol from MeOH/tetrahydrofuran or EtOH and sublime it at 110-140o (bath) at 10-4 mm to give a yellow spot with ninhydrin which slowly turns purple [NMR: Bowden et al. J Chem Soc (C) 172 1968]. It can also be purified by dissolving in the minimum volume of hot H2O and adding EtOH dropwise until cloudy, cool, and colourless crystals separate; IR: max 3445w, 3000-2560w br, 2156w, 1635s and 1475s cm-1. [NMR: Jager & Frey Justus Liebigs Ann Chem 817 1982.] Alternatively it has been purified by two successive chromatographic treatments on Dowex-1 x 8, with the first elution with 2M AcOH and a second with a linear gradient between 0—2M AcOH, evaporating the desired fractions and recrystallising the residue from MeOH. [McCarry & Savard Tetrahedron Lett 22 5153 1981, Nakamura Chem Pharm Bull Jpn 19 46 1971.]
References
[1] SUSAN M. J. DUNN Rick P T. Reconstruction of purified GABAA receptors: Ligand binding and chloride transporting properties[J]. Biochemistry Biochemistry, 1994, 33 3: 755-763. DOI: 10.1021/bi00169a017
[2] DONGXIAN ZHANG. Structure and function of GABA(C) receptors: a comparison of native versus recombinant receptors.[J]. Trends in pharmacological sciences, 2001, 29 1: 121-132. DOI: 10.1016/s0165-6147(00)01625-4
[3] JULIAN WHITE . Mushroom poisoning: A proposed new clinical classification[J]. Toxicon, 2019, 157: Pages 53-65. DOI: 10.1016/j.toxicon.2018.11.007
[4] J. SCHEEL-KRüGER J. A A V Christensen. Muscimol differentially facilitates stereotypy but antagonizes motility induced by dopaminergic drugs: A complex GABA-dopamine interaction[J]. Life sciences, 1978, 22 1: Pages 75-84. DOI: 10.1016/0024-3205(78)90414-9
[5] M. PARRAMóN M. P G. Pharmacological modulation of adrenal medullary GABAA receptor: consistent with its subunit composition[J]. British Journal of Pharmacology, 1995, 116 2: 1875-1881. DOI: 10.1111/j.1476-5381.1995.tb16676.x
[6] P KROGSGAARD-LARSEN K F B Frlund. GABA uptake inhibitors. Design, molecular pharmacology and therapeutic aspects.[J]. Current pharmaceutical design, 2000, 6 12: 1193-1209. DOI: 10.2174/1381612003399608
[7] MAJID JAFARI-SABET Iman J D. Muscimol state-dependent memory: Involvement of dorsal hippocampal μ-opioid receptors[J]. Behavioural Brain Research, 2009, 202 1: Pages 5-10. DOI: 10.1016/j.bbr.2009.03.010
[8] NEIL R GLEASON. The GABAA agonist muscimol attenuates induced airway constriction in guinea pigs in vivo.[J]. Journal of applied physiology, 2009, 106 4: 1257-1263. DOI: 10.1152/japplphysiol.91314.2008
MUSCIMOL Preparation Products And Raw materials
Raw materials
Preparation Products
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