product

61-54-1, tryptamine

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Product Tags

Names

Name tryptamine
Synonym More Synonyms

 tryptamine Biological Activity

Description Tryptamine is a monoamine alkaloid, similar to other trace amines, is believed to play a role as a neuromodulator or neurotransmitter.
Related Catalog
Target

Human Endogenous Metabolite

References

[1]. Jones RS, et al. Tryptamine: a neuromodulator or neurotransmitter in mammalian brain? Prog Neurobiol. 1982;19(1-2):117-39.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 378.8±0.0 °C at 760 mmHg
Melting Point 113-116 °C(lit.)
Molecular Formula C10H12N2
Molecular Weight 160.216
Flash Point 187.7±8.1 °C
Exact Mass 160.100052
PSA 41.81000
LogP 1.38
Vapour Pressure 0.0±0.8 mmHg at 25°C
Index of Refraction 1.669
Water Solubility negligible

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
NL4020000
CHEMICAL NAME :
Indole, 3-(2-aminoethyl)-
CAS REGISTRY NUMBER :
61-54-1
BEILSTEIN REFERENCE NO. :
0125513
LAST UPDATED :
199612
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C10-H12-N2
MOLECULAR WEIGHT :
160.24
WISWESSER LINE NOTATION :
T56 BMJ D2Z

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 – Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent – rat
DOSE/DURATION :
223 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPMSAE Journal of Pharmaceutical Sciences. (American Pharmaceutical Assoc., 2215 Constitution Ave., NW, Washington, DC 20037) V.50- 1961- Volume(issue)/page/year: 66,1692,1977
TYPE OF TEST :
LD50 – Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent – mouse
DOSE/DURATION :
100 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
EJMCA5 European Journal of Medicinal Chemistry–Chimie Therapeutique. (Editions Scientifiques Elsevier, 29 rue Buffon, F-75005, Paris, France) V.9- 1974- Volume(issue)/page/year: 9,453,1974
TYPE OF TEST :
LD50 – Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent – mouse
DOSE/DURATION :
500 mg/kg
TOXIC EFFECTS :
Behavioral – somnolence (general depressed activity)
REFERENCE :
DPHFAK Dissertationes Pharmaceuticae et Pharmacologicae. (Warsaw, Poland) V.18-24, 1966-72. For publisher information, see PJPPAA. Volume(issue)/page/year: 22,313,1970

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Risk Phrases 20/21/22-36/37/38-41-37/38-22
Safety Phrases S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS NL4020000
HS Code 29339990

 Synthetic Route

Previous 1/16 Next

N-acetyltryptamine structure

N-acetyltryptam…

1016-47-3

~80%

 

tryptamine structure

tryptamine

61-54-1

Literature: Shimizu, Yuhei; Morimoto, Hiroyuki; Zhang, Ming; Ohshima, Takashi Angewandte Chemie – International Edition, 2012 , vol. 51, # 34 p. 8564 – 8567
indole-3-glyoxylyl chloride structure

indole-3-glyoxy…

22980-09-2

~%

 

tryptamine structure

tryptamine

61-54-1

Literature: Journal of the Chinese Chemical Society, , vol. 54, # 5 p. 1363 – 1368
2-[2-(1H-indol-3-yl)ethyl]isoindole-1,3-dione structure

2-[2-(1H-indol-...

15741-71-6

~%

 

tryptamine structure

tryptamine

61-54-1

Literature: Bioorganic and Medicinal Chemistry Letters, , vol. 20, # 1 p. 157 - 160

 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%

 Articles54

More Articles

Use of Commercial Dry Yeast Products Rich in Mannoproteins for White and Rosé Sparkling Wine Elaboration.

J. Agric. Food Chem. 63 , 5670-81, (2015)

In sparkling wines, mannoproteins released during yeast autolysis largely affect their final quality. This process is very slow and may take several months. The aim of this work was to study the effec…

Enantioselective formal synthesis of ent-rhynchophylline and ent-isorhynchophylline.

Chem. Commun. (Camb.) 49(19) , 1954-6, (2013)

Starting from (S)-tryptophanol, a formal synthesis of ent-rhynchophylline and ent-isorhynchophylline, involving stereoselective cyclocondensation, spirocyclization, and alkylation reactions, and the f…

A separation of tyramine on a 2-(4-methoxyphenyl)ethylamine imprinted polymer: an answer from theoretical and experimental studies.

Talanta 129 , 155-64, (2014)

A 2-(4-methoxyphenyl)ethylamine imprinted polymer (MIP) was successfully applied for the selective separation of tyramine. A computational analysis was used to predict the affinity of the polymer matr…

 Synonyms

2-(1H-Indol-3-yl)ethylamine
Tryptamine
1H-Indole-3-ethanamine
2-indol-3-yl-ethylamine
Indole-ethylamine
L-TRYPTAMINE
EINECS 200-510-5
2-Indol-3-yl-aethylamin
Tryptamin
3-Indoleethanamine
2-(1H-Indol-3-yl)ethanamine
MFCD00005661
TRYPTAMINE(P)
125513
T56 BMJ D2Z
[2-(1H-indol-3-yl)-ethyl]amine
TRIPTAMINE
(1H-indol-3-yl)ethanamine
2-indol-3-ylethylamine

 

 

 

 

Names

Name tryptamine
Synonym More Synonyms

 tryptamine Biological Activity

Description Tryptamine is a monoamine alkaloid, similar to other trace amines, is believed to play a role as a neuromodulator or neurotransmitter.
Related Catalog
Target

Human Endogenous Metabolite

References

[1]. Jones RS, et al. Tryptamine: a neuromodulator or neurotransmitter in mammalian brain? Prog Neurobiol. 1982;19(1-2):117-39.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 378.8±0.0 °C at 760 mmHg
Melting Point 113-116 °C(lit.)
Molecular Formula C10H12N2
Molecular Weight 160.216
Flash Point 187.7±8.1 °C
Exact Mass 160.100052
PSA 41.81000
LogP 1.38
Vapour Pressure 0.0±0.8 mmHg at 25°C
Index of Refraction 1.669
Water Solubility negligible

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
NL4020000
CHEMICAL NAME :
Indole, 3-(2-aminoethyl)-
CAS REGISTRY NUMBER :
61-54-1
BEILSTEIN REFERENCE NO. :
0125513
LAST UPDATED :
199612
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C10-H12-N2
MOLECULAR WEIGHT :
160.24
WISWESSER LINE NOTATION :
T56 BMJ D2Z

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 – Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent – rat
DOSE/DURATION :
223 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPMSAE Journal of Pharmaceutical Sciences. (American Pharmaceutical Assoc., 2215 Constitution Ave., NW, Washington, DC 20037) V.50- 1961- Volume(issue)/page/year: 66,1692,1977
TYPE OF TEST :
LD50 – Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent – mouse
DOSE/DURATION :
100 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
EJMCA5 European Journal of Medicinal Chemistry–Chimie Therapeutique. (Editions Scientifiques Elsevier, 29 rue Buffon, F-75005, Paris, France) V.9- 1974- Volume(issue)/page/year: 9,453,1974
TYPE OF TEST :
LD50 – Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent – mouse
DOSE/DURATION :
500 mg/kg
TOXIC EFFECTS :
Behavioral – somnolence (general depressed activity)
REFERENCE :
DPHFAK Dissertationes Pharmaceuticae et Pharmacologicae. (Warsaw, Poland) V.18-24, 1966-72. For publisher information, see PJPPAA. Volume(issue)/page/year: 22,313,1970

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Risk Phrases 20/21/22-36/37/38-41-37/38-22
Safety Phrases S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS NL4020000
HS Code 29339990

 Synthetic Route

Previous 1/16 Next

N-acetyltryptamine structure

N-acetyltryptam…

1016-47-3

~80%

 

tryptamine structure

tryptamine

61-54-1

Literature: Shimizu, Yuhei; Morimoto, Hiroyuki; Zhang, Ming; Ohshima, Takashi Angewandte Chemie – International Edition, 2012 , vol. 51, # 34 p. 8564 – 8567
indole-3-glyoxylyl chloride structure

indole-3-glyoxy…

22980-09-2

~%

 

tryptamine structure

tryptamine

61-54-1

Literature: Journal of the Chinese Chemical Society, , vol. 54, # 5 p. 1363 – 1368
2-[2-(1H-indol-3-yl)ethyl]isoindole-1,3-dione structure

2-[2-(1H-indol-...

15741-71-6

~%

 

tryptamine structure

tryptamine

61-54-1

Literature: Bioorganic and Medicinal Chemistry Letters, , vol. 20, # 1 p. 157 - 160

 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%

 Articles54

More Articles

Use of Commercial Dry Yeast Products Rich in Mannoproteins for White and Rosé Sparkling Wine Elaboration.

J. Agric. Food Chem. 63 , 5670-81, (2015)

In sparkling wines, mannoproteins released during yeast autolysis largely affect their final quality. This process is very slow and may take several months. The aim of this work was to study the effec…

Enantioselective formal synthesis of ent-rhynchophylline and ent-isorhynchophylline.

Chem. Commun. (Camb.) 49(19) , 1954-6, (2013)

Starting from (S)-tryptophanol, a formal synthesis of ent-rhynchophylline and ent-isorhynchophylline, involving stereoselective cyclocondensation, spirocyclization, and alkylation reactions, and the f…

A separation of tyramine on a 2-(4-methoxyphenyl)ethylamine imprinted polymer: an answer from theoretical and experimental studies.

Talanta 129 , 155-64, (2014)

A 2-(4-methoxyphenyl)ethylamine imprinted polymer (MIP) was successfully applied for the selective separation of tyramine. A computational analysis was used to predict the affinity of the polymer matr…

 Synonyms

2-(1H-Indol-3-yl)ethylamine
Tryptamine
1H-Indole-3-ethanamine
2-indol-3-yl-ethylamine
Indole-ethylamine
L-TRYPTAMINE
EINECS 200-510-5
2-Indol-3-yl-aethylamin
Tryptamin
3-Indoleethanamine
2-(1H-Indol-3-yl)ethanamine
MFCD00005661
TRYPTAMINE(P)
125513
T56 BMJ D2Z
[2-(1H-indol-3-yl)-ethyl]amine
TRIPTAMINE
(1H-indol-3-yl)ethanamine
2-indol-3-ylethylamine

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