6-Hydroxyindole structure
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Common Name | 6-Hydroxyindole | ||
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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 |
Signal Word | Danger |
Use of 6-Hydroxyindole6-Hydroxyindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | 1H-indol-6-ol |
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Synonym | More Synonyms |
Description | 6-Hydroxyindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog |
Density | 1.3±0.1 g/cm3 |
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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 |
Storage condition | Keep Cold |
Symbol |
GHS05, GHS07, GHS09 |
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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 |
Precursor 8 | |
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DownStream 4 | |
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... |
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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... |
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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... |
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 |