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Tryptamine hydrochloride_Molecular_structure_CAS_343-94-2)
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Tryptamine hydrochloride

Catalog No. 246557 Name Sigma Aldrich
CAS Number 343-94-2 Website http://www.sigmaaldrich.com
M. F. C10H13ClN2 Telephone 1-800-521-8956
M. W. 196.67662 Fax
Purity 99% Email
Storage Chembase ID: 102816

SYNONYMS

Title
色胺 盐酸盐
IUPAC name
2-(1H-indol-3-yl)ethan-1-amine hydrochloride
IUPAC Traditional name
tryptamine hydrochloride
Synonyms
2-(3-Indolyl)ethylamine hydrochloride
β-吲哚基乙胺 盐酸盐
3-(2-Aminoethyl)indole hydrochloride
3-(2-氨乙基)吲哚 盐酸盐

DATABASE IDS

CAS Number 343-94-2
EC Number 206-446-4
MDL Number MFCD00012682
Beilstein Number 3568419
PubChem SID 24278134

PROPERTIES

Empirical Formula (Hill Notation) C10H12N2 · HCl
Purity 99%
Melting Point 253-255 °C(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
RTECS NL4375000
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Vasoactive; may have a neuromodulator function.
Other Notes
Biogenic amine formed from the decarboxylation of tryptophan by L-aromatic amino acid decarboxylase.
Packaging
25 g in poly bottle
5 g in glass bottle
Application
Reactant for preparation of:
• Tryptamine derivatives as inhibitors against hepatitis B virus1
• Carbamoyl epipodophyllotoxins as potential antitumor agents2
• Anthranilic acid derivatives as CCK receptor antagonists3
• Brassinin derivatives as indoleamine 2,3-dioxygenase inhibitors4
• Antispasmodic agents5
• β-carbolinium cations as new antimalarial agents6
Description (简体中文)
Biochem/physiol Actions
具有血管活性;可能具有神经调质功能。
Other Notes
由色氨酸经 L-芳香氨基酸脱羧酶作用进行脱羧而形成的生物胺。
包装
25 g in poly bottle
5 g in glass bottle
Application
Reactant for preparation of:
• Tryptamine derivatives as inhibitors against hepatitis B virus1
• Carbamoyl epipodophyllotoxins as potential antitumor agents2
• Anthranilic acid derivatives as CCK receptor antagonists3
• Brassinin derivatives as indoleamine 2,3-dioxygenase inhibitors4
• Antispasmodic agents5
• β-carbolinium cations as new antimalarial agents6

REFERENCES