N-Acetyltryptamine

Modify Date: 2025-08-20 11:14:24

N-Acetyltryptamine Structure
N-Acetyltryptamine structure
Common Name N-Acetyltryptamine
CAS Number 1016-47-3 Molecular Weight 202.25200
Density 1.164 g/cm3 Boiling Point 484.7ºC at 760 mmHg
Molecular Formula C12H14N2O Melting Point N/A
MSDS Chinese USA Flash Point 246.9ºC

 Use of N-Acetyltryptamine


N-Acetyltryptamine is a partial agonist for melatonin receptors in the retina[1]. N-Acetyltryptamine is also used for determination of serotonin N-acetyl transferase activity[2].

 Names

Name N-acetyltryptamine
Synonym More Synonyms

 N-Acetyltryptamine Biological Activity

Description N-Acetyltryptamine is a partial agonist for melatonin receptors in the retina[1]. N-Acetyltryptamine is also used for determination of serotonin N-acetyl transferase activity[2].
Related Catalog
References

[1]. Sugden D, et al. Melatonin receptor pharmacology: toward subtype specificity. Biol Cell. 1997 Nov;89(8):531-7.

[2]. De Angelis J, et al. Kinetic analysis of the catalytic mechanism of serotonin N-acetyltransferase (EC 2.3.1.87). J Biol Chem. 1998 Jan 30;273(5):3045-50.

 Chemical & Physical Properties

Density 1.164 g/cm3
Boiling Point 484.7ºC at 760 mmHg
Molecular Formula C12H14N2O
Molecular Weight 202.25200
Flash Point 246.9ºC
Exact Mass 202.11100
PSA 44.89000
LogP 2.23740
Vapour Pressure 1.51E-09mmHg at 25°C
Index of Refraction 1.619

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
HS Code 2933990090

 Synthetic Route

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles24

More Articles
Chloroplastic and cytoplasmic overexpression of sheep serotonin N-acetyltransferase in transgenic rice plants is associated with low melatonin production despite high enzyme activity.

J. Pineal Res. 58(4) , 461-9, (2015)

Serotonin N-acetyltransferase (SNAT), the penultimate enzyme in melatonin biosynthesis, catalyzes the conversion of serotonin into N-acetylserotonin. Plant SNAT is localized in chloroplasts. To test S...

Serine residues 110 and 114 are required for agonist binding but not antagonist binding to the melatonin MT(1) receptor.

Biochem. Biophys. Res. Commun. 282(5) , 1229-36, (2001)

Site-directed mutation of serine 110 (Ser(3.35)) and serine 114 (Ser(3.39)) in the human melatonin MT(1) receptor to alanine residues reduced ligand binding affinities of seven known melatonin recepto...

[The biosynthesis of low-molecular-weight nitrogen-containing secondary metabolite-alkaloids by the resident strains of Penicillium chrysogenum and Penicillium expansum isolated on the board of the Mir space station ].

Mikrobiologiia 71(6) , 773-7, (2002)

The analysis of the absorption spectra of the low-molecular-weight nitrogen-containing secondary metabolites--alkaloids--of 4 Penicillium chrysogenum strains and 6 Penicillium expansum strains isolate...

 Synonyms

N-[2-(1H-indol-3-yl)ethyl]acetamide
Tocris-0357
Chicago Sky Blue 6B
N-Acetyltryptamine
N-(2-(1H-Indol-3-yl)ethyl)acetamide
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here



Get all suppliers and price by the below link:

N-Acetyltryptamine suppliers

N-Acetyltryptamine price

Related Compounds: More...
N-Acetyltryptamine
154164-30-4
5-Amino-N-acetyltryptamine
393835-65-9
5-NITRO-N-ACETYLTRYPTAMINE
96735-08-9
2-Benzyl-N-acetyltryptamine
117946-91-5
5-Hydroxy-N-acetyltryptamine
1210-83-9
5-Acetoxy-N-acetyltryptamine
28026-16-6
5-hydroxyethoxy-N-acetyltryptamine
214416-49-6
2-Benzyl-5-methoxy-N-acetyltryptamine
122853-28-5
5-Methoxycarbonylamino-N-acetyltryptamine
190277-13-5
N-(3-fluorophenyl)-2-((1-(2-(4-methylpiperidin-1-yl)-2-oxoethyl)-1H-indol-3-yl)sulfonyl)acetamide
878059-43-9
N-(4-fluorophenyl)-2-((1-(2-(4-methylpiperidin-1-yl)-2-oxoethyl)-1H-indol-3-yl)sulfonyl)acetamide
878059-46-2
N-(3-chlorophenyl)-2-((1-(2-(4-methylpiperidin-1-yl)-2-oxoethyl)-1H-indol-3-yl)sulfonyl)acetamide
878059-49-5
N-(4-chlorophenyl)-2-((1-(2-(4-methylpiperidin-1-yl)-2-oxoethyl)-1H-indol-3-yl)sulfonyl)acetamide
878059-52-0
N-(2,4-difluorophenyl)-2-((1-(2-(4-methylpiperidin-1-yl)-2-oxoethyl)-1H-indol-3-yl)sulfonyl)acetamide
878059-60-0
N-(3-chloro-4-methylphenyl)-2-((1-(2-(4-methylpiperidin-1-yl)-2-oxoethyl)-1H-indol-3-yl)sulfonyl)acetamide
878059-64-4
N-(5-chloro-2-methoxyphenyl)-2-((1-(2-(4-methylpiperidin-1-yl)-2-oxoethyl)-1H-indol-3-yl)sulfonyl)acetamide
878059-68-8
N-(2-methoxyphenyl)-2-((1-(2-(4-methylpiperidin-1-yl)-2-oxoethyl)-1H-indol-3-yl)sulfonyl)acetamide
878059-72-4
N-(3-methoxyphenyl)-2-((1-(2-(4-methylpiperidin-1-yl)-2-oxoethyl)-1H-indol-3-yl)sulfonyl)acetamide
878059-76-8
N-(2-ethoxyphenyl)-2-((1-(2-(4-methylpiperidin-1-yl)-2-oxoethyl)-1H-indol-3-yl)sulfonyl)acetamide
878059-84-8