D-Tryptophanol
D-Tryptophanol (CAS: 52485-52-6, Formula: C11H14N2O, MW: 190.24 g/mol) is a chiral amino alcohol derived from the essential amino acid L-tryptophan. It serves as a valuable chiral building block and intermediate in organic synthesis. Characterised by its optical activity ([α]20/D +18.5°, c = 1 in methanol), D-Tryptophanol is primarily employed in the synthesis of complex molecules, including pharmaceuticals and biologically active compounds.

Chiral Building Block
D-Tryptophanol is utilised as a stereochemically defined synthon for constructing chiral molecules. Its specific configuration makes it suitable for asymmetric synthesis, particularly in the development of pharmaceuticals where stereochemistry is critical for efficacy.
Pharmaceutical Intermediate
This compound functions as an intermediate in the synthesis pathways of various pharmaceutical agents. Its structural features can be incorporated into drug candidates targeting diverse therapeutic areas.
Chemical Biology Research
In chemical biology, D-Tryptophanol can be employed in the development of probes or modified biomolecules. Its availability facilitates studies into biological processes involving tryptophan derivatives.
Peptide Chemistry
As a derivative of tryptophan, D-Tryptophanol may find applications in modifying peptides. This can be useful for altering peptide stability, receptor binding, or biological activity.
| Molecular weight | 190.24 |
|---|---|
| Empirical formula | C11H14N2O |
| Assay | 97% |
| Optical activity | [α]20/D +18.5°, c = 1 in methanol |
| Melting point | 86-89 °C(lit.) |
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is D-Tryptophanol used for?
+
D-Tryptophanol is primarily used as a chiral building block and intermediate in organic synthesis, particularly for pharmaceuticals and in chemical biology research.
What is the CAS number and chemical formula for D-Tryptophanol?
+
The CAS number for D-Tryptophanol is 52485-52-6, and its chemical formula is C11H14N2O.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies D-Tryptophanol with an assay of 97%. We do not represent this product as USP, BP, EP or any other pharmacopoeia grade unless explicitly stated in the product specifications.
What are the safety and handling considerations for D-Tryptophanol?
+
D-Tryptophanol is classified under WGK 3 in Germany, indicating a high hazard to water. Handle with appropriate personal protective equipment in a well-ventilated area to avoid exposure. Refer to the Safety Data Sheet for comprehensive handling information.
How is D-Tryptophanol packed and shipped?
+
D-Tryptophanol is carefully packed to ensure stability during transit. Tech Serve Solutions exports this chemical globally, adhering to all relevant shipping regulations.
How can I request a quote or sample for D-Tryptophanol?
+
To request a quote or a sample of D-Tryptophanol, please contact our sales department through the website or by calling us directly.
▶ Related products

1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis

1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis