Identification | More | [Name]
Serotonin hydrochloride | [CAS]
153-98-0 | [Synonyms]
3-(2-AMINOETHYL)-5-HYDROXYINDOLE HYDROCHLORIDE 3-(2-AMINOETHYL)-5-INDOLOL HYDROCHLORIDE 5-HT 5-HYDROXY-3-(2-AMINOETHYL)INDOLE HYDROCHLORIDE 5-HYDROXYTRYPTAMINE HCL 5-HYDROXYTRYPTAMINE HYDROCHLORIDE SERATONIN HYDROCHLORIDE SEROTONIN HCL SEROTONIN HYDROCHLORIDE TIMTEC-BB SBB003418 5-HYDROXYTRYPTAMINE HYDROCHLORIDE 99% SEROTONIN HYDROCHLORIDE 99% 5-Hydroxytrptamine HCl SEROTONINEHYDROCHLORIDE SEROTONIN HYDROCHLORIDE(RG) 3-(2-Aminoethyl)-5-hydroxyindole hydrochloride, 5-HT, 5-Hydroxytryptamine hydrochloride Serotonin hydrochloride ,99% | [EINECS(EC#)]
244-464-4 | [Molecular Formula]
C10H13ClN2O | [MDL Number]
MFCD00012686 | [Molecular Weight]
212.68 | [MOL File]
153-98-0.mol |
Chemical Properties | Back Directory | [Appearance]
white to cream powder | [Melting point ]
149-154 °C(lit.) | [storage temp. ]
2-8°C
| [solubility ]
H2O: 17 mg/mL
| [form ]
powder
| [color ]
white to off-white
| [Stability:]
Stable, but light sensitive and hygroscopic. Incompatible with strong oxidizing agents. | [Water Solubility ]
soluble | [Sensitive ]
Light Sensitive & Hygroscopic | [Merck ]
14,8463 | [BRN ]
3570963 | [InChIKey]
MDIGAZPGKJFIAH-UHFFFAOYSA-N | [CAS DataBase Reference]
153-98-0(CAS DataBase Reference) | [Storage Precautions]
Light sensitive |
Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S22:Do not breathe dust . S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . | [RIDADR ]
UN2811 | [WGK Germany ]
3
| [RTECS ]
NM2571000 | [F ]
3-8-10 | [HazardClass ]
6.1 | [PackingGroup ]
III | [HS Code ]
29339900 |
Hazard Information | Back Directory | [Chemical Properties]
white to cream powder | [Uses]
A neurotransmitter. | [Uses]
Neurotransmitter;5-HT agonist | [Uses]
Serotonin hydrochloride is used as a neurotransmitter and function as an endogenous serotonin receptor agonist in various biochemical processes. It is an active component, which is used to regulate the mood, emesis, cognition and appetite in vivo. | [Uses]
Serotonin is a monoamine neurotransmitter that is biochemically derived from tryptophan and produced in serotonergic neurons in the central nervous system and in enterochromaffin cells in the gastrointestinal tract. Serotonin is important in the regulation of mood, sleep, vomiting, sexuality, and appetite. Low levels of serotonin are associated with several disorders, including depression, migraines, bipolar disorder, and anxiety. Its actions are terminated primarily via uptake of serotonin from the synapse. Serotonin reuptake can be inhibited with MDMA, cocaine, tricyclic antidepressants, and selective serotonin reuptake inhibitors.[Cayman Chemical] | [Uses]
Serotonin is a monoamine neurotransmitter. | [Definition]
ChEBI:Serotonin hydrochloride is a member of tryptamines. It is functionally related to a serotonin. | [Biological Activity]
Endogenous agonist at 5-HT receptors and endogenous substrate for 5-HT transporters. Neurotransmitter that has roles in regulation of mood, emesis, sexuality, sleep and appetite in vivo . | [Biochem/physiol Actions]
Neurotransmitter. | [storage]
Store at 2-8°C, protect from light | [Purification Methods]
5-HT is purified by recrystallisation from EtOH/Et2O or Et2O to give the hygroscopic salt. Store it in the dark as it is light sensitive. The free base has m 84-86o (from Et2O). The 5-benzyloxy derivative has m 84-86o (from Et2O). [Ek & Witkop J Am Chem Soc 76 5579 1954, Hamlin & Fischer J Am Chem Soc 73 5007 1951.] The picrate 1H2O has m 196-197.5o (dec with sintering at 160-165o) after crystallisation from Et2O. Serotonin is a natural neurotransmitter [Chuang Life Sci 41 1051 1987]. [Beilstein 22/12 V 16.] |
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