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Indole-3-Carboxylic Acid

HCID 69867
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Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
771-50-6
Standard SMILES
O=C(O)c1c[nH]c2ccccc12
InChIKey
KMAKOBLIOCQGJP-UHFFFAOYSA-N
Molecular formula
C9H7NO2
Average molar mass
161.16 g/mol
Monoisotopic mass
161.04767847

Overview

Indole-3-carboxylic acid is an indole-3-carboxylic acid carrying a carboxy group at position 3. It has a role as a bacterial metabolite and a human metabolite. It is a conjugate acid of an indole-3-carboxylate.

Names & identifiers

Preferred name
Indole-3-Carboxylic Acid
IUPAC
1H-indole-3-carboxylic acid
English name
Indole-3-carboxylic acid
Molecular formula
C9H7NO2
Molecular weight
161.16

Names & synonyms

Indole-3-carboxylic acid1H-Indole-3-carboxylic acid771-50-63-CarboxyindoleCHEBI:2480959711R38B0DTXSID50227886RefChem:923413DTXCID00150377212-231-63-Indoleformic acid3-Indolecarboxylic acid
Show more names
ICOe-3-carboxyL3-Indoleformic3-indoleic acid3-IndolecarboxylicIndol-3-carbonsureIndole-3-carboxylic
3-IndolecarboxylateMFCD000056243-Indoleformate3-Indolylcarboxylic acid3-IndolylcarboxylateEINECS 212-231-6Indole - 3 Carboxylic acid.beta.-Indolylcarboxylic acid

Database identifiers

CAS
771-50-6
PubChem CID
69867
DTXSID
DTXSID50227886
ChEMBL
CHEMBL387527
ChEBI
CHEBI:24809
UNII
59711R38B0
EC Number
212-231-6
Nikkaji
J113.034J

Properties

Computed structural propertiesFilling in

XLogP
2
Topological polar surface area
53.1 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
2
Rotatable bonds
1
Heavy atoms
12
Formal charge
0
Complexity
193

Experimental & physicochemical properties

LogP · 2 items

1.99

1.99

Melting Point206.5 °C
Physical DescriptionSolid
Collision Cross Section124.5 Ų [M-H]- [CCS Type: DT; Method: single field calibrated with Agilent tune mix (Agilent)]

Physicochemical properties

Melting point
232 · 232-234 °C (dec.)(lit.)
Boiling point
287.44 °C · 287.44°C (rough estimate)
Density
1.248 · 1.2480 (rough estimate)
refractive index
1.505 · 1.5050 (estimate)
storage temp.
2 · 2-8°C
solubility
95 % · Soluble in 95% Ethanol: 50 mg/ml, also soluble in methanol.
pka
3.9 · 3.90±0.10(Predicted)
form

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 4 items

Warning

H302 (40%): Harmful if swallowed [Warning Acute toxicity, oral]

P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 10 reports by companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Hazard information

Hazard Classes and CategoriesAcute Tox. 4 (40%)

Safety data

PPE
Eyeshields, Gloves, type N95 (US)
wgk
3
rtecs
NK7882892
hs_code
29339900
risk_code
36/37/38-21/22
Signal word
Warning
Symbol(GHS)
GHS07
hazard_code
Xn,Xi
safety_code
22-24/25-36/37/39-26
hazard_class
IRRITANT
Storage Class
11 - Combustible Solids
Hazard statements
H315-H319-H335
Precautionary statements
P261-P280a-P304+P340-P305+P351+P338-P405-P501a

Chemistry & industry

Pharmacology

Metabolism/Metabolites3-Indole carboxylic acid has known human metabolites that include 3-Indole carboxylic acid glucuronide.
Applications · 2 items

DescriptionIndole-3-carboxylic acid is a plant metabolite derived from tryptophan that has been found in Arabidopsis and has diverse biological activities.1,2,3,4 It induces resistance in Arabidopsis against the plant necrotrophic fungus P. cucumerina when applied as a soil-drenching solution at a concentration of 150 µM prior to infection.2 Indole-3-carboxylic acid is cytotoxic to A549 human lung and MCF-7 human breast cancer cells (EC50s = 4.6 and 12.9 µg/ml, respectively) and inhibits HIV replication in infected H9 lymphocytes (IC50 = 16.4 µg/ml).3 Indole-3-carboxylic acid has also been used as a precursor in the synthesis of substituted thiadiazoles with anticancer activity.4WARNING This product is not for human or veterinary use.

General DescriptionThe structures of the derivatives of indole-3-carboxylic acid were studied using gas chromatography with high resolution mass spectrometry (GC-HRMS), ultra-high performance liquid chromatography in combination with high resolution tandem mass spectrometry (UHPLC-HRMS), nuclear magnetic resonance spectroscopy (NMR) and Fourier transform infrared spectroscopy (FT-IR).

Preparation methods · 1 item

Preparationindole-3-carboxylic acid can be synthesized by the hydrolysis reaction of 3-trichloroacetyl indole: add 235g 3-trichloroacetyl indole into 1000ml methanol, slowly drop an appropriate amount of 50% KOH solution, heat up and reflux for 18 hours, cool to room temperature, The methanol was recovered by concentration, and the residual liquid was left; 1500 ml of water was added to the residual liquid, hydrochloric acid was added dropwise to adjust pH=3~4, and then filtered, and the solid obtained by filtration was dried to obtain 144g of indole-3-carboxylic acid crude product; The crude product was slurried with 100g of ethyl acetate for 25 minutes,filtered and dried to obtain indole-3-carboxylic acid (137g, yield 91.8%).

Related reactions

147 records
New reaction record
HRID 5367 reaction equation
HRID 5367As reactantuspto-grants-1993_09
HRID 5380 reaction equation
HRID 5380As reactantuspto-grants-1993_09
HRID 5383 reaction equation
HRID 5383As reactantuspto-grants-1993_09
HRID 5386 reaction equation
HRID 5386As reactantuspto-grants-1993_09
HRID 20202 reaction equation
HRID 20202As reactantuspto-grants-2010_06
HRID 23413 reaction equation
HRID 23413As reactantuspto-grants-2005_02
HRID 55929 reaction equation
HRID 55929As reactantuspto-grants-2016_09
HRID 61962 reaction equation
HRID 61962As reactantuspto-grants-2016_09
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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Powder
color
Light beige
BRN
129435 · 129435
InChI
InChI=1S/C9H7NO2/c11-9(12)7-5-10-8-4-2-1-3-6(7)8/h1-5,10H,(H,11,12)
InChIKey
KMAKOBLIOCQGJP-UHFFFAOYSA-N
SMILES
N1C2=C(C=CC=C2)C(C(O)=O)=C1
CAS DataBase Reference
771 · 771-50-6(CAS DataBase Reference)
EWG's Food Scores
1 · 1
FDA UNII
59711 R38B0 · 59711R38B0
UNSPSC Code
41116107 · 41116107
NACRES
24 · NA.24
Symbol(GHS)
7 · GHS07
Signal word
Warning
Hazard statements
315 · H315-H319-H335
Precautionary statements
261 · P261-P280a-P304+P340-P305+P351+P338-P405-P501a
PPE
95 · Eyeshields, Gloves, type N95 (US)
Hazard Codes
Xn,Xi
Risk Statements
36 · 36/37/38-21/22
Safety Statements
22 · 22-24/25-36/37/39-26
WGK Germany
3 · 3
RTECS
7882892 · NK7882892
HazardClass
IRRITANT
HS Code
29339900 · 29339900
Storage Class
11 · 11 - Combustible Solids

Upstream & downstream products

Upstream raw materials

4-(Benzyloxy)pyridine N-oxideMethyl indole-3-carboxylate3-Bromoindole1-Benzylindole-3-carboxylic acid3-(Trifluoroacetyl)indole3-Trichloroacetylindole

Downstream products

1-Methyl-1H-indole-3-carboxylic acidIndole-2-carboxylic acid3-Aminoindole HCl1-(Pivaloyloxymethyl)-1H-indole-3-carboxylic acid1H-Indole-3-carboxaMide, N-(2-chlorophenyl)-N-Methoxy-N-methyl-1H-indole-3-carboxamide1-pentyl-1H-indole-3-carboxylic acid

Additional notes

DefinitionChEBI: Indole-3-carboxylic acid is an indole-3-carboxylic acid carrying a carboxy group at position 3. It has a role as a human metabolite and a bacterial metabolite. It is a conjugate acid of an indole-3-carboxylate.