6-Hydroxyindole

Modify Date: 2025-08-25 15:46:58

6-Hydroxyindole Structure
6-Hydroxyindole structure
Common Name 6-Hydroxyindole
CAS Number 2380-86-1 Molecular Weight 133.15
Density 1.3±0.1 g/cm3 Boiling Point 343.2±15.0 °C at 760 mmHg
Molecular Formula C8H7NO Melting Point 124-130 °C
MSDS Chinese USA Flash Point 161.4±20.4 °C
Symbol GHS05 GHS07 GHS09
GHS05, GHS07, GHS09
Signal Word Danger

 Use of 6-Hydroxyindole


6-Hydroxyindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name 1H-indol-6-ol
Synonym More Synonyms

 6-Hydroxyindole Biological Activity

Description 6-Hydroxyindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 343.2±15.0 °C at 760 mmHg
Melting Point 124-130 °C
Molecular Formula C8H7NO
Molecular Weight 133.15
Flash Point 161.4±20.4 °C
Exact Mass 133.052765
PSA 36.02000
LogP 1.41
Vapour Pressure 0.0±0.8 mmHg at 25°C
Index of Refraction 1.739
InChIKey XAWPKHNOFIWWNZ-UHFFFAOYSA-N
SMILES Oc1ccc2cc[nH]c2c1
Storage condition Keep Cold

 Safety Information

Symbol GHS05 GHS07 GHS09
GHS05, GHS07, GHS09
Signal Word Danger
Hazard Statements H302-H317-H318-H411
Precautionary Statements P273-P280-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Faceshields;Gloves
Hazard Codes Xi:Irritant
Risk Phrases R22;R41;R43;R51/53
Safety Phrases S37/39-S26-S61-S24-S2
RIDADR UN 3077
Hazard Class 9.0

 Synthetic Route

 Articles4

More Articles
Determination of selected synthetic cannabinoids and their metabolites by micellar electrokinetic chromatography--mass spectrometry employing perfluoroheptanoic acid-based micellar phase.

Talanta 150 , 568-76, (2016)

Perfluoroheptanoic acid was employed as a volatile micellar phase in background electrolyte for micellar electrokinetic chromatography-tandem mass spectrometry separation and determination of 15 selec...

Inhibitory effect of hydroxyindoles and their analogues on human melanoma tyrosinase.

Z. Naturforsch., C, J. Biosci. 65 , 49-54, (2010)

A recent study showed that N-acylserotonin derivatives have strong inhibitory activity against tyrosinase. To clarify the role of the 5-hydroxy group in the indole ring, 2-, 4-, 5-, 6-, and 7-hydroxyi...

Albumin stimulates the activity of the human UDP-glucuronosyltransferases 1A7, 1A8, 1A10, 2A1 and 2B15, but the effects are enzyme and substrate dependent.

PLoS ONE 8(1) , e54767, (2013)

Human UDP-glucuronosyltransferases (UGTs) are important enzymes in metabolic elimination of endo- and xenobiotics. It was recently shown that addition of fatty acid free bovine serum albumin (BSA) sig...

 Synonyms

indolol
6-hydroxy-1h-indole
1H-Indol-6-ol
6-Hydroxyindole
EINECS 417-020-4
indol-6-ol
6-monohydroxyindole
6-hydroxy-indole
6-indolol
MFCD00152101
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