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162698

Sigma-Aldrich

DL-Tryptophan

≥99% (HPLC)

All Photos(3)
Synonym(s):
(±)-α-Amino-3-indolepropionic acid, (±)-2-Amino-3-(3-indolyl)propionic acid, DL-3β-Indolylalanine
Empirical Formula (Hill Notation):
C11H12N2O2
CAS Number:
54-12-6
Molecular Weight:
204.23
Beilstein:
86199
EC Number:
200-194-9
MDL number:
MFCD00064339
PubChem Substance ID:
24850000
NACRES:
NA.22

Quality Level

200

Assay

≥99% (HPLC)

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

mp

289-290 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

NC(Cc1c[nH]c2ccccc12)C(O)=O

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)

InChI key

QIVBCDIJIAJPQS-UHFFFAOYSA-N

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This Item
T3300469971470031
DL-Tryptophan ≥99% (HPLC)

Sigma-Aldrich

162698

DL-Tryptophan

DL-Tryptophan ≥99% (HPLC)

Sigma-Aldrich

T3300

DL-Tryptophan

L-Tryptophanol 97%

Sigma-Aldrich

469971

L-Tryptophanol

D-Tryptophanol 97%

Sigma-Aldrich

470031

D-Tryptophanol

form

powder

form

powder

form

-

form

-

mp

289-290 °C (dec.) (lit.)

mp

289-290 °C (dec.) (lit.)

mp

73-77 °C (lit.)

mp

86-89 °C (lit.)

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

100

reaction suitability

reaction type: solution phase peptide synthesis

reaction suitability

-

reaction suitability

reaction type: solution phase peptide synthesis

reaction suitability

reaction type: solution phase peptide synthesis

application(s)

peptide synthesis

application(s)

-

application(s)

peptide synthesis

application(s)

peptide synthesis

General description

DL-Tryptophan also known as 2-amino-3-(1H-indol-3-yl)-propionic acid, is commonly used in peptide synthesis.

Application

DL-Tryptophan is used as a starting material for the preparation of N-acyl monoisotripeptides via solution-phase peptide synthesis.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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S Liaqat, et.al.
Synthesis, 46, 67-72 (2014)
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As a continuation of our research efforts toward the development of tryptophan-based radiotracers for tumor imaging with positron emission tomography (PET), three new fluoroethoxy tryptophan analogues were synthesized and evaluated in vivo. These new tracers (namely, 4-(2-[(18)F]fluoroethoxy)-dl-tryptophan ([(18)F]4-FEHTP), 6-(2-[(18)F]fluoroethoxy)-dl-tryptophan ([(18)F]6-FEHTP)
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