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Merck
CN

I5508

DL-Indole-3-lactic acid

99%

Synonym(s):

β-(3-Indolyl)lactic acid, 2-Hydroxy-3-(3-indolyl)propanoic acid, 3-(3-Indolyl)-2-hydroxypropanoic acid, 3-Indolyllactic acid, Indolelactic acid

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About This Item

Empirical Formula (Hill Notation):
C11H11NO3
CAS Number:
Molecular Weight:
205.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-627-9
MDL number:
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Product Name

DL-Indole-3-lactic acid, 99%

InChI key

XGILAAMKEQUXLS-UHFFFAOYSA-N

InChI

1S/C11H11NO3/c13-10(11(14)15)5-7-6-12-9-4-2-1-3-8(7)9/h1-4,6,10,12-13H,5H2,(H,14,15)

SMILES string

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

assay

99%

mp

145-146 °C (lit.)

Quality Level

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Application

Reactant for preparation of:
  • Antibacterial agents
  • Dietary sweetener

General description

DL-Indole-3-lactic acid can serve as a building block in the synthesis of various molecules, like Indole-3-acetic acid (IAA)

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Determination of urinary 5-hydroxyindole-3-acetic acid using solid-phase extraction and reversed-phase high-performance liquid chromatography with electrochemical detection.
P P Chou et al.
Journal of chromatography, 341(1), 167-171 (1985-05-31)
Francisco A Moreno et al.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 20(1), 18-24 (2009-11-10)
The purpose of this study was to examine the differential effects of acute tryptophan (TRP) depletion vs. sham condition on plasma, cerebrospinal fluid (CSF) biochemical parameters, and mood in the following three subject groups: (1) nine antidepressant-free individuals with remitted
Soumen K Manna et al.
Journal of proteome research, 9(8), 4176-4188 (2010-06-15)
Alcohol-induced liver disease (ALD) is a leading cause of nonaccident-related deaths in the United States. Although liver damage caused by ALD is reversible when discovered at the earlier stages, current risk assessment tools are relatively nonspecific. Identification of an early
S Krásenský et al.
Electrophoresis, 16(6), 968-973 (1995-06-01)
A new approach is described for highly sensitive chiral analyses by capillary zone electrophoresis, based on using an on-line combination of two capillaries filled with either chiral selective or achiral background electrolytes (BGE). Thus, the BGEs are selected in such
Bioconversion of biologically active indole derivatives with indole-3-acetic acid-degrading enzymes from Caballeronia glathei DSM50014
M Sadauskas, et al.
Biomolecules, 10, 663-663 (2020)

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