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Merck

I5508

Sigma-Aldrich

DL-Indole-3-lactic acid

99%

Sinónimos:

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

Fórmula empírica (notación de Hill):
C11H11NO3
Número de CAS:
Peso molecular:
205.21
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

mp

145-146 °C (lit.)

SMILES string

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

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)

InChI key

XGILAAMKEQUXLS-UHFFFAOYSA-N

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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)

Application

Reactant for preparation of:
  • Antibacterial agents
  • Dietary sweetener

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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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
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)
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X Liu et al.
The Journal of biological chemistry, 269(1), 668-675 (1994-01-07)
The hormone, auxin, plays an important role in the differentiation and growth of plant cells. A number of auxin-responsive genes have been characterized but until now minimal auxin-responsive cis-elements within these promoter regions have not been identified. Here we show

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