| Chemical & Physical Properties | |
|---|---|
| CAS Number | 4350-07-6 |
| Catalog No. | 2A-0099654 |
| Chinese Name | 5-羟基-D-色氨酸 |
| Synonyms | (2R)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid; D-5-HTP (D-2-Amino-3-(5-hydroxyindolyl)propionic acid; C11H12N2O3; HRP |
| Molecular Formula | C11H11O3N1 |
| Molecular Weight | 205.21 |
| Purity | 96+ |
| Melting Point | 27ºC |
| Application | D-5-hydroxytryptophan (D-5-HTP) is the D-isomer of 5-HTP and can be separated from DL-5-hydroxytryptophan through continuous separation [1]. |
| EINECS | 0 |
| HTC | 2933990090 |
| UN(IATA) | 0 |
| MDL Number | MFCD26960776 |
| SMILES | NC(Cc1c[nH]c2ccc(O)cc12)C(=O)O |
| InChI | InChI=1S/C11H12N2O3/c12-9(11(15)16)3-6-5-13-10-2-1-7(14)4-8(6)10/h1-2,4-5,9,13-14H,3,12H2,(H,15,16)/t9-/m1/s1 |
| InChI Key | LDCYZAJDBXYCGN-SECBINFHSA-N |
| Hazard Symbols | transportation |
| MSDS | msds/99654_1_4350_07_6.pdf |
| Bioactivity | D-5-Hydroxytryptophan (D-5-HTP) is the D-isomers of 5-HTP, and can be isolated from DL-5-hydroxytryptophan by successive separations[1]. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Neurological Disease References [1]. J Arendt, et al. Alternative pathways of 5-hydroxyindole metabolism. II. The role transamination in the metabolism of D-5-hydroxytryptophan in the rat. Biochem Pharmacol. 1967 Mar;16(3):419-22. Chemical & Physical Properties Melting Point 27ºC Molecular Formula C11H12N2O3 Molecular Weight 220.22500 Exact Mass 220.08500 PSA 99.34000 LogP 1.52820 InChIKey LDCYZAJDBXYCGN-SECBINFHSA-N SMILES NC(Cc1c[nH]c2ccc(O)cc12)C(=O)O |
| Use of | D-5-Hydroxytryptophan (D-5-HTP) is the D-isomers of 5-HTP, and can be isolated from DL-5-hydroxytryptophan by successive separations[1]. Properties Name 5-hydroxy-D-tryptophan Synonym More Synonyms Biological Activity Description D-5-Hydroxytryptophan (D-5-HTP) is the D-isomers of 5-HTP, and can be isolated from DL-5-hydroxytryptophan by successive separations[1]. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Neurological Disease References [1]. J Arendt, et al. Alternative pathways of 5-hydroxyindole metabolism. II. The role transamination in the metabolism of D-5-hydroxytryptophan in the rat. Biochem Pharmacol. 1967 Mar;16(3):419-22. Chemical & Physical Properties Molecular Formula C11H12N2O3 Exact Mass 220.08500 PSA 99.34000 LogP 1.52820 InChIKey LDCYZAJDBXYCGN-SECBINFHSA-N |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 20.0% |
| Transport Info | Product name: 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% |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods 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: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-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 reminder to users No data available |
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