4-Hydroxyindole structure
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Common Name | 4-Hydroxyindole | ||
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CAS Number | 2380-94-1 | Molecular Weight | 133.147 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 343.2±15.0 °C at 760 mmHg | |
Molecular Formula | C8H7NO | Melting Point | 97-99 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 161.4±20.4 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of 4-Hydroxyindole4-Hydroxyindole is a member of the class of hydroxyindoles that is 1H-indole substituted by a hydroxy group at position 4. 4-Hydroxyindole is an important raw material or intermediate in the synthesis of pharmaceutical products and industrial polymers[1]. |
Name | 4-hydroxyindole |
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Synonym | More Synonyms |
Description | 4-Hydroxyindole is a member of the class of hydroxyindoles that is 1H-indole substituted by a hydroxy group at position 4. 4-Hydroxyindole is an important raw material or intermediate in the synthesis of pharmaceutical products and industrial polymers[1]. |
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Related Catalog | |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 343.2±15.0 °C at 760 mmHg |
Melting Point | 97-99 °C(lit.) |
Molecular Formula | C8H7NO |
Molecular Weight | 133.147 |
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 | 0-6°C |
Water Solubility | slightly soluble |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi:Irritant |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36-S37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2933990090 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2933990090 |
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Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Characterization of in vitro metabolites of JWH-018, JWH-073 and their 4-methyl derivatives, markers of the abuse of these synthetic cannabinoids
J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 957 , 68-76, (2014) • Optimization of a suitable extraction protocol for alkylindoles and their metabolites from biological fluids. • Detection of alkylindoles and their metabolites by means of the GC/MS method adopted b... |
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Validation and application of an UPLC-MS/MS method for the quantification of synthetic cannabinoids in urine samples and analysis of seized materials from the Portuguese market.
Forensic Sci. Int. 243 , 117-25, (2014) An UPLC-MS/MS method using ESI+ionization and MRM was developed and fully validated according to international guidelines for the qualitative and quantitative analysis of nine synthetic cannabinoids a... |
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Glucuronidation of psilocin and 4-hydroxyindole by the human UDP-glucuronosyltransferases.
Drug Metab. Dispos. 38(3) , 386-95, (2010) We have examined the glucuronidation of psilocin, a hallucinogenic indole alkaloid, by the 19 recombinant human UDP-glucuronosyltransferases (UGTs) of subfamilies 1A, 2A, and 2B. The glucuronidation o... |
1H-Indol-4-ol |
4-Hydroxylndole |
1H-Indol-7-ol |
EINECS 219-177-2 |
indol-4-ol |
7-Hydroxyindol |
7-HYDROXYLINDOLE |
4-hydroxy-indole |
INDOL-7-OL |
7-HYDROXY-1H-INDOLE |
7-monohydroxyindole |
7-hydroxyindole |
1H-INDOLE-4-OL |
4-Hydroxxyindole |
7-Indolol |
MFCD00005667 |
4-Hydroxyindole |
4-hydroxy-1H-indole |
4-INDOLOL |