Sodium bromide
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Names |
IUPAC name
Sodium bromide
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Identifiers |
CAS Registry Number
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7647-15-6 Y
13466-08-5 (dihydrate) N |
ChEMBL |
ChEMBL1644694 N |
ChemSpider |
22712 Y |
InChI
-
InChI=1S/BrH.Na/h1H;/q;+1/p-1 Y
Key: JHJLBTNAGRQEKS-UHFFFAOYSA-M Y
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InChI=1/BrH.Na/h1H;/q;+1/p-1
Key: JHJLBTNAGRQEKS-REWHXWOFAR
|
Jmol-3D images |
Image |
PubChem |
253881 |
RTECS number |
VZ3150000 |
|
UNII |
LC1V549NOM Y |
Properties |
Chemical formula
|
BrNa |
Molar mass |
102.89 g·mol−1 |
Appearance |
White powder, hygroscopic |
Density |
3.21 g/cm3 (anhydrous)
2.18 g/cm3 (dihydrate) |
Melting point |
747 °C (1,377 °F; 1,020 K)
(anhydrous)
36 °C (97 °F; 309 K)
(dihydrate) decomposes[3] |
Boiling point |
1,390 °C (2,530 °F; 1,660 K) [3] |
Solubility in water
|
71.35 g/100 mL (−20 °C)
79.52 g/100 mL (0 °C)
94.32 g/100 mL (25 °C)[1]
104.9 g/100 mL (40 °C)
116.2 g/100 mL (100 °C)[2] |
Solubility |
Soluble in alcohol, liquid ammonia, pyridine, hydrazine, SO2, amine
Insoluble in acetone, acetonitrile[1] |
Solubility in methanol |
17.3 g/100 g (0 °C)
16.8 g/100 g (20 °C)
16.1 g/100 g (40 °C)
15.3 g/100 g (60 °C)[1] |
Solubility in ethanol |
2.45 g/100 g (0 °C)
2.32 g/100 g (20 °C)
2.29 g/100 g (30 °C)
2.35 g/100 g (70 °C)[1] |
Solubility in formic acid |
19.3 g/100 g (18 °C)
19.4 g/100 g (25 °C)[1] |
Solubility in glycerol |
38.7 g/100 g (20 °C)[1] |
Solubility in dimethylformamide |
3.2 g/100 g (10.3 °C)[1] |
Vapor pressure |
1 torr (806 °C)
5 torr (903 °C)[3] |
Thermal conductivity |
5.6 W/m·K (150 K)[4] |
Refractive index (nD)
|
1.6428 (24 °C)
nKrF = 1.8467 (24 °C)
nHe–Ne = 1.6389 (24 °C)[5] |
Viscosity |
1.42 cP (762 °C)
1.08 cP (857 °C)
0.96 cP (937 °C)[1] |
Structure |
Crystal structure
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Cubic |
Lattice constant
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a = 5.97 Å[4]
|
Thermochemistry |
Specific
heat capacity (C)
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51.4 J/mol·K[1] |
Std molar
entropy (So298)
|
86.82 J/mol·K[1] |
Std enthalpy of
formation (ΔfHo298)
|
−361.41 kJ/mol[1] |
Gibbs free energy (ΔfG˚)
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−349.3 kJ/mol[1] |
Hazards |
Safety data sheet |
External MSDS |
EU Index |
Not listed |
R-phrases |
R36 |
S-phrases |
(S2), S24/25, S46 |
NFPA 704 |
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Flash point |
800 °C (1,470 °F; 1,070 K) |
Lethal dose or concentration (LD, LC): |
LD50 (Median dose)
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3500 mg/kg (rats, oral) |
Related compounds |
Other anions
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Sodium fluoride
Sodium chloride
Sodium iodide |
Other cations
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Lithium bromide
Potassium bromide
Rubidium bromide
Caesium bromide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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N verify (what is: Y/N?) |
Infobox references |
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Sodium bromide is an inorganic compound with the formula NaBr. It is a high-melting white, crystalline solid that resembles sodium chloride. It is a widely used source of the bromide ion and has many applications.[7]
Contents
- 1 Synthesis, structure, reactions
- 2 Applications
- 2.1 Medicine
- 2.2 Preparation of other bromine compounds
- 2.3 Disinfectant
- 2.4 Petroleum industry
- 3 Safety
- 4 References
- 5 External links
Synthesis, structure, reactions
NaBr crystallizes in the same cubic motif as NaCl, NaF and NaI. The anhydrous salt crystallizes above 50.7 °C.[7] Dihydrate salts (NaBr·2H2O) begins to anhydrous at 50.7 °C in water solution.[2]
It is produced by treating sodium hydroxide with hydrogen bromide.
Sodium bromide can be used as a source of the chemical element bromine. This can be accomplished by treating an aqueous solution of NaBr with chlorine gas:
- 2 NaBr + Cl2 → Br2 + 2 NaCl
Applications
Sodium bromide is the most useful inorganic bromide in industry.[7] It is also used as a catalyst in TEMPO-mediated oxidation reactions.[8]
Medicine
See also: Potassium bromide § Medical and Veterinary
Also known as Sedoneural, sodium bromide has been used as a hypnotic, anticonvulsant, and sedative in medicine, widely used as an anticonvulsant and a sedative in the late 19th and early 20th centuries. Its action is due to the bromide ion, and for this reason potassium bromide is equally effective. In 1975, bromides were removed from drugs in the U.S. such as Bromo-Seltzer due to toxicity.[9]
Preparation of other bromine compounds
Sodium bromide is widely used for the preparation of other bromides in organic synthesis and other areas. It is a source of the bromide nucleophile to convert alkyl chlorides to more reactive alkyl bromides by the Finkelstein reaction:
- NaBr + RCl → RBr + NaCl (R = alkyl)
Once a large need in photography, but now shrinking, the photosensitive salt silver bromide is prepared using NaBr.
Disinfectant
Sodium bromide is used in conjunction with chlorine as a disinfectant for swimming pools.
Petroleum industry
Sodium bromide is used to prepare dense fluids used in oil wells.
Safety
NaBr has a very low toxicity with an oral LD50 estimated at 3.5 g/kg for rats.[6] However, this is a single-dose value. Bromide ion is a cumulative toxin with a relatively long half life (in excess of a week in humans): see potassium bromide.
References
- ^ a b c d e f g h i j k l http://chemister.ru/Database/properties-en.php?dbid=1&id=714
- ^ a b Seidell, Atherton; Linke, William F. (1919). Solubilities of Inorganic and Organic Compounds (2nd ed.). D. Van Nostrand Company.
- ^ a b c Pradyot, Patnaik (2003). Handbook of Inorganic Chemicals. The McGraw-Hill Companies, Inc. ISBN 0-07-049439-8.
- ^ a b "Sodium Bromide (NaBr)". http://www.korth.de. Korth Kristalle GmbH. Retrieved 2014-06-11.
- ^ Polyanskiy, Mikhail. "Refractive index of NaBr (Sodium bromide) - Li". http://www.refractiveindex.info. Retrieved 2014-06-11.
- ^ a b "Sodium bromide MSDS" (PDF). http://www.sciencelab.com. Sciencelab.com, Inc. 2013-05-21. Retrieved 2014-06-11.
- ^ a b c Michael J. Dagani, Henry J. Barda, Theodore J. Benya, David C. Sanders "Bromine Compounds" in Ullmann's Encyclopedia of Industrial Chemistry Wiley-VCH, Weinheim, 2000. doi:10.1002/14356007.a04_405
- ^ http://link.springer.com/article/10.1007/s10570-009-9381-2#page-1
- ^ "Bromide: Potassium & Sodium". http://www.canine-epilepsy.com. Canine-Epilepsy Resources. 2011-05-31. Retrieved 2014-06-11.
External links
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Wikimedia Commons has media related to Sodium bromide. |
- Information about NaBr.
- Bromide Poisoning in Angola
Sodium compounds
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- NaAlO2
- NaBH4
- NaBH3(CN)
- NaBO2
- NaBiO3
- NaBr
- NaBrO
- NaBrO3
- NaCH3COO
- NaC6H5CO2
- NaC6H4(OH)CO2
- NaCN
- NaCl
- NaClO
- NaClO2
- NaClO3
- NaClO4
- NaF
- NaFO
- Na2FeO4
- NaH
- NaHCO3
- NaH2PO4
- NaHSO3
- NaHSO4
- NaI
- NaIO3
- NaIO4
- Na5IO6
- NaMnO4
- NaN3
- NaNH2
- NaNO2
- NaNO3
- NaOCN
- NaO2
- NaO3
- NaOH
- NaPO2H2
- NaReO4
- NaSCN
- NaSH
- NaTcO4
- NaVO3
- Na2CO2
- Na2CO3
- Na4CO4
- Na2C2O4
- Na2CrO4
- Na2Cr2O7
- Na2GeO3
- Na2MnO4
- Na3MnO4
- Na2MoO4
- Na2MoS4
- Na2N2O2
- Na2O
- Na2O2
- Na2O(UO3)2
- Na2PO3F
- Na2S
- Na2SO3
- Na2SO4
- Na2S2O3
- Na2S2O4
- Na2S2O5
- Na2S2O6
- Na2S2O7
- Na2S2O8
- Na2Se
- Na2SeO3
- Na2SeO4
- Na2SiO3
- Na2Si2O5
- Na4SiO4
- Na2Te
- Na2TeO3
- Na2Po
- Na2Ti3O7
- Na2U2O7
- NaWO4
- Na2Zn(OH)4
- Na3N
- Na3P
- Na3PO4
- Na3VO4
- Na4Fe(CN)6
- Na4P3O7
- Na5P3O10
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Chemical formulas
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Hypnotics/sedatives (N05C)
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GABAA |
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GABAB
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- 1,4-Butanediol
- Aceburic acid
- GABOB
- GHB (sodium oxybate)
- GBL
- GVL
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H1 |
Antihistamines |
- Captodiame
- Cyproheptadine
- Diphenhydramine
- Doxylamine
- Hydroxyzine
- Methapyrilene
- Pheniramine
- Promethazine
- Propiomazine
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Antidepressants |
- Tricyclic antidepressants
- Amitriptyline
- Doxepin
- Trimipramine, etc.
- Tetracyclic antidepressants
- Mianserin
- Mirtazapine, etc.
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Antipsychotics |
- Typical antipsychotics
- Chlorpromazine
- Thioridazine, etc.
- Atypical antipsychotics
- Olanzapine
- Quetiapine
- Risperidone, etc.
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α2-Adrenergic |
- Clonidine
- Detomidine
- Dexmedetomidine
- Lofexidine
- Medetomidine
- Romifidine
- Tizanidine
- Xylazine
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5-HT2A |
Antidepressants |
- Trazodone
- Tricyclic antidepressants
- Amitriptyline
- Doxepin
- Trimipramine, etc.
- Tetracyclic antidepressants
- Mianserin
- Mirtazapine, etc.
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Antipsychotics |
- Typical antipsychotics
- Chlorpromazine
- Thioridazine, etc.
- Atypical antipsychotics
- Olanzapine
- Quetiapine
- Risperidone, etc.
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Others |
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Melatonin |
- Agomelatine
- Melatonin
- Ramelteon
- Tasimelteon
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Orexin |
- Almorexant
- Filorexant
- Suvorexant
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Others |
- Acecarbromal
- Apronal
- Bromisoval
- Cannabidiol
- Carbromal
- Diethylpropanediol
- Embutramide
- Evoxine
- Fenadiazole
- Gabapentin
- Kavalactones
- Mephenoxalone
- Metaglycodol
- Niaprazine
- Opioids
- Passion flower
- Phenaglycodol
- Scopolamine
- UMB68
- Valnoctamide
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Index of psychology and psychiatry
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Description |
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Disorders |
- Mental and behavioral
- Mood
- Developmental
- pervasive
- dyslexia and specific
- Substance-related
- Emotional and behavioral
- Symptoms and signs
- Evaluation and testing
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Treatment |
- Psychotherapy
- Drugs
- depression
- antipsychotics
- anxiety
- dementia
- hypnotics and sedatives
- psychostimulants, ADHD and nootropics
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Anticonvulsants (N03)
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GABAergics |
GABAAR PAMs |
- Barbiturates: Barbexaclone
- Metharbital
- Methylphenobarbital
- Pentobarbital
- Phenobarbital#
- Primidone; Carbamates: Felbamate; Benzodiazepines: Clobazam
- Clonazepam
- Clorazepate
- Diazepam#
- Lorazepam#
- Midazolam
- Nimetazepam
- Nitrazepam
- Temazepam; Others: Bromide (potassium bromide, sodium bromide)
- Paraldehyde
- Stiripentol
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GABA-T inhibitors |
- Fatty acids: Valproate
- Valpromide
- Valproate pivoxil; Others: Ethanolamine-O-sulfate
- Vigabatrin
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Others |
- GABAR agonists: Progabide; GAT-1 inhibitors: Tiagabine
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Channelergics |
Sodium blockers |
- Hydantoins: Ethotoin
- Fosphenytoin
- Mephenytoin
- Phenytoin#; Ureas: Phenacemide
- Pheneturide; Fatty acids: Valproic acid# (sodium valproate, valproate semisodium)
- Valpromide
- Valproate pivoxil; Carboxamides: Carbamazepine#
- Eslicarbazepine acetate
- Oxcarbazepine; Others: Lacosamide
- Lamotrigine
- Rufinamide
- Topiramate
- Zonisamide
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Calcium blockers |
- Oxazolidinediones: Ethadione
- Paramethadione
- Trimethadione; Succinimides: Ethosuximide#
- Mesuximide
- Phensuximide; Gabapentinoids: Gabapentin
- Pregabalin; Others: Lamotrigine
- Topiramate
- Zonisamide
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Potassium openers |
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Others |
CA inhibitors |
- Sulfonamides: Acetazolamide
- Ethoxzolamide
- Sultiame
- Topiramate
- Zonisamide
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Others |
- Beclamide
- Levetiracetam
- Perampanel
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
Index of psychology and psychiatry
|
|
Description |
|
|
Disorders |
- Mental and behavioral
- Mood
- Developmental
- pervasive
- dyslexia and specific
- Substance-related
- Emotional and behavioral
- Symptoms and signs
- Evaluation and testing
|
|
Treatment |
- Psychotherapy
- Drugs
- depression
- antipsychotics
- anxiety
- dementia
- hypnotics and sedatives
- psychostimulants, ADHD and nootropics
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GABAA receptor positive allosteric modulators
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Alcohols |
- Brometone
- Butanol
- Chloralodol
- Chlorobutanol (cloretone)
- Ethanol (drinking alcohol)
- Ethchlorvynol
- Isobutanol
- Isopropanol
- Menthol
- Methanol
- Methylpentynol
- Pentanol
- Petrichloral
- Propanol
- tert-Butanol (2M2P)
- tert-Pentanol (2M2B)
- Tribromoethanol
- Trichloroethanol
- Triclofos
- Trifluoroethanol
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Barbiturates |
- (-)-DMBB
- Allobarbital
- Alphenal
- Amobarbital
- Aprobarbital
- Barbexaclone
- Barbital
- Benzobarbital
- Benzylbutylbarbiturate
- Brallobarbital
- Brophebarbital
- Butabarbital/Secbutabarbital
- Butalbital
- Buthalital
- Butobarbital
- Butallylonal
- Carbubarb
- CP-1414S
- Crotylbarbital
- Cyclobarbital
- Cyclopentobarbital
- Difebarbamate
- Enallylpropymal
- Ethallobarbital
- Eterobarb
- Febarbamate
- Heptabarb
- Heptobarbital
- Hexethal
- Hexobarbital
- Metharbital
- Methitural
- Methohexital
- Methylphenobarbital
- Narcobarbital
- Nealbarbital
- Pentobarbital
- Phenallymal
- Phenobarbital
- Phetharbital
- Primidone
- Probarbital
- Propallylonal
- Propylbarbital
- Proxibarbital
- Reposal
- Secobarbital
- Sigmodal
- Spirobarbital
- Talbutal
- Tetrabamate
- Tetrabarbital
- Thialbarbital
- Thiamylal
- Thiobarbital
- Thiobutabarbital
- Thiopental
- Thiotetrabarbital
- Valofane
- Vinbarbital
- Vinylbital
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Benzodiazepines |
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Carbamates |
- Carisbamate
- Carisoprodol
- Clocental
- Cyclarbamate
- Difebarbamate
- Emylcamate
- Ethinamate
- Febarbamate
- Felbamate
- Hexapropymate
- Lorbamate
- Mebutamate
- Meprobamate
- Methocarbamol
- Nisobamate
- Pentabamate
- Phenprobamate
- Procymate
- Styramate
- Tetrabamate
- Tybamate
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Flavonoids |
- 6-Methylapigenin
- Ampelopsin (dihydromyricetin)
- Apigenin
- Baicalein
- Baicalin
- Catechin
- EGC
- EGCG
- Hispidulin
- Linarin
- Luteolin
- Rc-OMe
- Skullcap constituents (e.g., baicalin)
- Wogonin
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Imidazoles |
- Etomidate
- Metomidate
- Propoxate
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Kava constituents |
- 10-Methoxyyangonin
- 11-Methoxyyangonin
- 11-Hydroxyyangonin
- Desmethoxyyangonin
- 11-Methoxy-12-hydroxydehydrokavain
- 7,8-Dihydroyangonin
- Kavain
- 5-Hydroxykavain
- 5,6-Dihydroyangonin
- 7,8-Dihydrokavain
- 5,6,7,8-Tetrahydroyangonin
- 5,6-Dehydromethysticin
- Methysticin
- 7,8-Dihydromethysticin
- Yangonin
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Neuroactive steroids |
- Acebrochol
- Allopregnanolone
- Alfadolone
- Alfaxalone
- 3α-Androstanediol
- Androsterone
- Cholesterol
- DHDOC
- 5α-DHP
- Etiocholanolone
- Ganaxolone
- Hydroxydione
- Minaxolone
- Org 20599
- Org 21465
- Pregnanolone (eltanolone)
- Renanolone
- SAGE-217
- SAGE-689
- THDOC
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Nonbenzodiazepines |
- β-Carbolines: Abecarnil
- Gedocarnil
- Harmane
- SL-651,498
- ZK-93423; Cyclopyrrolones: Eszopiclone
- Pagoclone
- Pazinaclone
- Suproclone
- Suriclone
- Zopiclone; Imidazopyridines: Alpidem
- DS-1
- Necopidem
- Saripidem
- Zolpidem; Pyrazolopyrimidines: Divaplon
- Fasiplon
- Indiplon
- Lorediplon
- Ocinaplon
- Panadiplon
- Taniplon
- Zaleplon; Others: Adipiplon
- CGS-8216
- CGS-9896
- CGS-13767
- CGS-20625
- CL-218,872
- CP-615,003
- CTP-354
- ELB-139
- GBLD-345
- JM-1232
- L-838,417
- Lirequinil (Ro41-3696)
- NS-2664
- NS-2710
- NS-11394
- Pipequaline
- ROD-188
- RWJ-51204
- SB-205,384
- SX-3228
- TP-003
- TPA-023
- TP-13
- U-89843A
- U-90042
- Y-23684
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Phenols |
- Fospropofol
- Propofol
- Thymol
|
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Piperidinediones |
- Glutethimide
- Methyprylon
- Piperidione
- Pyrithyldione
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Pyrazolopyridines |
- Cartazolate
- Etazolate
- ICI-190,622
- Tracazolate
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Quinazolinones |
- Afloqualone
- Cloroqualone
- Diproqualone
- Etaqualone
- Mebroqualone
- Mecloqualone
- Methaqualone
- Methylmethaqualone
- Nitromethaqualone
- SL-164
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Volatiles/gases |
- Acetone
- Acetophenone
- Acetylglycinamide chloral hydrate
- Aliflurane
- Benzene
- Butane
- Butylene
- Centalun
- Chloral
- Chloral betaine
- Chloral hydrate
- Chloroform
- Cryofluorane
- Desflurane
- Dichloralphenazone
- Dichloromethane
- Diethyl ether
- Enflurane
- Ethyl chloride
- Ethylene
- Fluroxene
- Gasoline
- Halopropane
- Halothane
- Isoflurane
- Kerosine
- Methoxyflurane
- Methoxypropane
- Nitric oxide
- Nitrogen
- Nitrous oxide
- Norflurane
- Paraldehyde
- Propane
- Propylene
- Roflurane
- Sevoflurane
- Synthane
- Teflurane
- Toluene
- Trichloroethane (methyl chloroform)
- Trichloroethylene
- Vinyl ether
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Others/unsorted |
- 3-Hydroxybutanal
- α-EMTBL
- AA-29504
- Avermectins (e.g., ivermectin)
- Bromide compounds (e.g., lithium bromide, potassium bromide, sodium bromide)
- Carbamazepine
- Chloralose
- Chlormezanone
- Clomethiazole
- DEABL
- Dihydroergolines (e.g., dihydroergocryptine, dihydroergosine, dihydroergotamine, ergoloid (dihydroergotoxine))
- DS2
- Efavirenz
- Etazepine
- Etifoxine
- Fenamates (e.g., flufenamic acid, mefenamic acid, niflumic acid, tolfenamic acid)
- Fluoxetine
- Flupirtine
- Hopantenic acid
- Lanthanum
- Lignans (e.g., 4-O-methylhonokiol, honokiol, magnolol, obovatol)
- Loreclezole
- Menthyl isovalerate (validolum)
- Monastrol
- Niacin
- Nicotinamide (niacinamide)
- Org 25,435
- Phenytoin
- Propanidid
- Retigabine (ezogabine)
- Safranal
- SAGE-547
- Seproxetine
- Stiripentol
- Sulfonylalkanes (e.g., sulfonmethane (sulfonal), tetronal, trional)
- Terpenoids (e.g., borneol)
- Topiramate
- Valerian constituents (e.g., isovaleric acid, valerenic acid, valerenol)
- Unsorted benzodiazepine site PAMs: MRK-409 (MK-0343)
- TCS-1105
- TCS-1205
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See also: GABAergics
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