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Merck
CN

134228

5-甲基色胺 盐酸盐

98%

别名:

3-(2-氨基乙基)-5-甲基吲哚 盐酸盐

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经验公式（希尔记法）:
C11H14N2 · HCl
化学文摘社编号:
1010-95-3
分子量:
210.70
EC 号:
213-777-8
MDL编号:
MFCD00012683
UNSPSC代码:
12352100
PubChem化学物质编号:
24848138
NACRES:
NA.22

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方案

98%

表单

powder

mp

289-292 °C (dec.) (lit.)

溶解性

H2O: soluble 50 mg/mL, clear, yellow

官能团

amine

SMILES字符串

Cl.Cc1ccc2[nH]cc(CCN)c2c1

InChI

1S/C11H14N2.ClH/c1-8-2-3-11-10(6-8)9(4-5-12)7-13-11;/h2-3,6-7,13H,4-5,12H2,1H3;1H

InChI key

RBHDFGBPJGEYCK-UHFFFAOYSA-N

相关类别

应用

5-Methyltryptamine hydrochloride was used to study the mechanism of metabolism of 9-methyl 1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine in rats. It was used as internal standard in the determination of urinary metabolites of 5-methoxy-N,N-diisopropyltryptamine in humans. It was used as reactant in:
  • synthesis of kinesin spindle protein (KSP) inhibitors
  • intramolecular furan Diels-Alder reactions
  • Pictet-Spengler-like reactions
  • reactant in synthesis of kinesin spindle protein (KSP) inhibitors
  • reactant in intramolecular furan Diels-Alder reactions
  • reactant in Pictet-Spengler-like reactions

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
STBD5596V
S21034
06703JE
08721BW
06830LD

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"Pictet-Spengler-like" Synthesis of Tetrahydro-beta-carbolines under Hydrolytic Conditions. Direct Use of Azalactones as Phenylacetaldehyde Equivalents.
James E. Audia et al.
The Journal of organic chemistry, 61(22), 7937-7939 (1996-11-01)
Ruan, X., et al.
Huaxue Xuebao, 66, 1731-1731 (2008)
O A Candia et al.
Biochimica et biophysica acta, 602(2), 389-400 (1980-11-04)
The effects of serotonin and five other indoles were tested on the electrical parameters and ionic transport in the isolated toad lens. Serotonin, tryptophan and 5-hydroxy-L-tryptophan did not affect the electrical parameters of the lens at concentrations as high as
Characterization of eight biogenic indoleamines as substrates for type A and type B monoamine oxidase.
O Suzuki et al.
Biochemical pharmacology, 30(11), 1353-1358 (1981-06-01)
J Sallés et al.
Psychopharmacology, 154(2), 115-125 (2001-04-21)
One of the major pathways for neurotransmitter signaling involves phosphoinositide-specific and G-protein-dependent phospholipase C-beta (PLC-beta), which stimulates the formation of inositol 1,4,5-trisphosphate and diacylglycerol. Serotonergic and muscarinic-cholinergic signals in the brain are largely mediated through the hydrolysis of phosphoinositides by
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