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L-Tryptophan

Catalog Number
ACM73223
Product Name
L-Tryptophan
Structure
L-Tryptophan
CAS
73-22-3
  • Product Overview
  • Documentation
  • Usage
Synonyms
L-Beta-3-indolylalanine
IUPAC Name
(2S)-2-Amino-3-(1H-indol-3-yl)propanoic acid
Molecular Weight
204.23
Molecular Formula
C11H12N2O2
InChI
InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)/t9-/m0/s1
InChI Key
QIVBCDIJIAJPQS-VIFPVBQESA-N
Boiling Point
342.72 °C
Melting Point
289-290 °C(lit.)
Purity
99%
Density
1.34 g/cm³
Solubility
Slightly soluble in acetic acid, ethanol, insoluble in ethyl ether
Appearance
White to yellow-white powder
Storage
2-8 °C
Assay
0.99
Color Form
Leaflets or plates from dilute alcohol;White to slightly yellowish-white ... crystals or crystalline powder;
Complexity
245
Covalently-Bonded Unit Count
1
Decomposition
When heated to decomposition it emits toxic fumes of /nitric oxide/.;
Defined Atom Stereocenter Count
1
EC Number
200-795-6
Exact Mass
204.089877630
H-Bond Acceptor
3
H-Bond Donor
3
Heavy Atom Count
15
Isomeric SMILES
C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)O)N
MDL Number
MFCD00064340
Monoisotopic Mass
204.089877630
NSC Number
757373
Odor
Odorless;
Other Experimental
Decomposes at 289 deg C (rapid heating);Needles from methanol, decomposes at 251 deg C /Tryptophan hydrochloride/;IR: 8612 (Sadtler Research Laboratories IR Grating Collection) /Tryptophan (DL)/;UV: 3453 (Sadtler Research Laboratories Spectral Collection) /Tryptophan (DL)/;1H NMR: 582 (Sadtler Research Laboratories Spectral Collection) /Tryptophan (DL)/;MASS: 1229 (National Bureau of Standards EPA-NIH Mass Spectra Data Base, NSRDS-NBS-63) /Tryptophan (DL)/;1H NMR: 582 (Sadtler Research Laboratories Spectral Collection) /Tryptophan (D)/;MASS: 1229 (National Bureau of Standards EPA-NIH Mass Spectra Data Base, NSRDS-NBS-63) /Tryptophan (D)/;
Physical State
Solid
Refractive Index
-32 ° (C=1, H₂O)
Rotatable Bond Count
3
Topological Polar Surface Area
79.1 Ų
UNII
8DUH1N11BX
Vapor Pressure
2.1X10-9 mm Hg at 25 deg C (est);
Application
Amino acids-type drug:

It can be used in amino acid infusion, being often combined with iron and vitamins. Its co-administration with VB6 can improve depression and prevention/treatment of skin disease; as a sleep sedative, it can be combined with L-dopa for the treatment of Parkinson's disease. It is carcinogenic to experimental animals; it may cause adverse reactions including nausea, anorexia and asthmas. Avoid combination with monoamine oxidase inhibitors.

Nutritional supplements:

Tryptophan contained in egg white protein, fish meat, corn meal and other amino acids are limited; content in cereals such as rice is also low. It can be combined with lysine, methionine and threonine for enhanced amino acids. It can be supplemented to corn product at the content of 0.02% tryptophan and 0.1% lysine, being capable of significantly improving the protein potency.tryptophan is one of the 21 amino acids comprising a protein. Tryptophan is a component of the skin's natural moisturizing factors.
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