CAS Number54-16-0
Synonyms5-Hydroxyindoleacetic acid; (5-Hydroxy-1H-indol-3-yl)acetic acid; 2-(5-Hydroxy-1H-indol-3-yl)acetic acid; (5-hydroxyindol-3-yl)acetic acid; 5-hydroxy-indole-3-acetic acid; EINECS 200-195-4; MFCD00005639; 5-Hydroxyindoleacetate; 5-Hydroxyindole-3-acetic Acid; 5-Hydroxyindolacetic Acid
Molecular FormulaC10H9NO3
Molecular Weight191.183
Purity98.00%
Density1.496±0.06 g/cm3
Boiling Point497.1±30.0 °C at 760 mmHg
Melting Point161-164ºC (dec.)(lit.)
AppearanceSolid;White to Amber to Dark purple powder to crystal
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 54-16-0 |
| Catalog No. | 2A-1166607 |
| Chinese Name | 5-羟基吲哚-3-乙酸 |
| Synonyms | 5-Hydroxyindoleacetic acid; (5-Hydroxy-1H-indol-3-yl)acetic acid; 2-(5-Hydroxy-1H-indol-3-yl)acetic acid; (5-hydroxyindol-3-yl)acetic acid; 5-hydroxy-indole-3-acetic acid; EINECS 200-195-4; MFCD00005639; 5-Hydroxyindoleacetate; 5-Hydroxyindole-3-acetic Acid; 5-Hydroxyindolacetic Acid |
| Molecular Formula | C10H9NO3 |
| Molecular Weight | 191.183 |
| Purity | 98.00 |
| Density | 1.496±0.06 g/cm3 |
| Boiling Point | 497.1±30.0 °C at 760 mmHg |
| Melting Point | 161-164ºC (dec.)(lit.) |
| Appearance | Solid;White to Amber to Dark purple powder to crystal |
| Water Solubility | Sparingly soluble (11 g/L) (25 ºC) |
| Storage Condition | This product should be sealed and stored in a dry |
| Application | 5-Hydroxyindole-3-acetic acid is the major metabolite of serotonin or metanephrine and is used as a biomarker for neuroendocrine tumors. |
| HTC | 2933990090 |
| PubChem ID | 7946 |
| SMILES | O=C(O)Cc1c[nH]c2ccc(O)cc12 |
| InChI | InChI=1S/C10H9NO3/c12-7-1-2-9-8(4-7)6(5-11-9)3-10(13)14/h1-2,4-5,11-12H,3H2,(H,13,14) |
| InChI Key | DUUGKQCEGZLZNO-UHFFFAOYSA-N |
| Hazard Symbols | transportation |
| Bioactivity | 5-Hydroxyindole-3-acetic acid is the main metabolite of serotonin or metanephrines, which can be used as a biomarker of neuroendocrine tumors. Related Catalog Research Areas >> Neurological Disease Natural Products >> Acids and Aldehydes Research Areas >> Cancer Target Human Endogenous Metabolite In Vitro 5-Hydroxyindole-3-acetic acid (5HIAA) is a metabolite issued from serotonin metabolism, and the latter is synthetized from the essential amino acid tryptophan. Serotonin is mainly metabolised by monoamine oxidase in the liver and the lungs[1]. References [1]. Corcuff JB, et al. Urinary sampling for 5HIAA and metanephrines determination: revisiting the recommendations. Endocr Connect. 2017 Aug;6(6):R87-R98. Chemical & Physical Properties Density 1.496±0.06 g/cm3 Boiling Point 497.1±30.0 °C at 760 mmHg Melting Point 161-164ºC (dec.)(lit.) Molecular Formula C10H9NO3 Molecular Weight 191.183 Flash Point 254.4±24.6 °C Exact Mass 191.058243 PSA 73.32000 LogP 0.26 Vapour Pressure 0.0±1.3 mmHg at 25°C Index of Refraction 1.740 InChIKey DUUGKQCEGZLZNO-UHFFFAOYSA-N SMILES O=C(O)Cc1c[nH]c2ccc(O)cc12 Water Solubility Sparingly soluble (11 g/L) (25 ºC) |
| Use of | 5-Hydroxyindole-3-acetic acid is the main metabolite of serotonin or metanephrines, which can be used as a biomarker of neuroendocrine tumors. Properties Articles43 Name (5-hydroxyindol-3-yl)acetic acid Synonym More Synonyms 5-Hydroxyindole-3-acetic acid Biological Activity Description 5-Hydroxyindole-3-acetic acid is the main metabolite of serotonin or metanephrines, which can be used as a biomarker of neuroendocrine tumors. Related Catalog Research Areas >> Neurological Disease Natural Products >> Acids and Aldehydes Research Areas >> Cancer Human Endogenous Metabolite In Vitro 5-Hydroxyindole-3-acetic acid (5HIAA) is a metabolite issued from serotonin metabolism, and the latter is synthetized from the essential amino acid tryptophan. Serotonin is mainly metabolised by monoamine oxidase in the liver and the lungs[1]. References [1]. Corcuff JB, et al. Urinary sampling for 5HIAA and metanephrines determination: revisiting the recommendations. Endocr Connect. 2017 Aug;6(6):R87-R98. Chemical & Physical Properties Molecular Formula C10H9NO3 Exact Mass 191.058243 PSA 73.32000 Index of Refraction 1.740 InChIKey DUUGKQCEGZLZNO-UHFFFAOYSA-N |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 20.0% |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: No dangerous goods IMDG Code: No dangerous goods International Air Transport Dangerous Regulations: No dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special precautions for users No data available The above information is believed to be correct, but is not all-inclusive and should be used as a guide only. The information in this document is based on our current knowledge and is Correct safety instructions apply to this product. This information does not represent a guarantee as to the properties of this product. The company is not responsible for any damage caused by any operation or contact with the above products. For more terms of use, see invoice or package The reverse side of the mounting strip. |
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