CAS Number538-09-0
Synonymsβ-Phenylethyl alcohol; b-Phenylethanol; β-Phenylethanol; 3a-Nortropanol; 2-Hydroxyethylbenzene; (3-endo)-8-Azabicyclo[3.2.1]octan-3-ol hydrochloride (1:1); Phenylethyl alcohol (USP); endo-8-azabicyclo(3.2.1)octan-3-ol hydrochloride; β-phenylethyl alcoho; 8-Aza-bicyclo[3.2.1]octan-3-ol HCl; b-pea; Nortropin; (2-Hydroxyethyl)benzene; 8-Azabicyclo[3.2.1]octan-3-ol; Tropigenin; nortropenol; phenylethanol; β-Phenethyl alcohol; b-Phenylethyl alcohol; (3-endo)-8-Azabicyclo[3.2.1]octan-3-olato(2-) hydrochloride (1:1); endo-8-Azabicyclo[3.2.1]octan-3-ol; nortropan-3endo-ol; N-Demethyltropine; PEA; N-normethyltropine; Benzeneethanol; Phenyl Ethanol; Q2R; 3-hydroxy-nortropan; NOR-TROPANOL
Molecular FormulaC7H13O1N1
Molecular Weight127.19
Purity99%
Density1.0±0.1 g/cm3
Boiling Point218.2±8.0 °C at 760 mmHg
Melting Point108-110ºC
Appearancelight yellowish brown solid
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 538-09-0 |
| Catalog No. | 2A-9011717 |
| Chinese Name | 去甲托品醇 |
| Synonyms | β-Phenylethyl alcohol; b-Phenylethanol; β-Phenylethanol; 3a-Nortropanol; 2-Hydroxyethylbenzene; (3-endo)-8-Azabicyclo[3.2.1]octan-3-ol hydrochloride (1:1); Phenylethyl alcohol (USP); endo-8-azabicyclo(3.2.1)octan-3-ol hydrochloride; β-phenylethyl alcoho; 8-Aza-bicyclo[3.2.1]octan-3-ol HCl; b-pea; Nortropin; (2-Hydroxyethyl)benzene; 8-Azabicyclo[3.2.1]octan-3-ol; Tropigenin; nortropenol; phenylethanol; β-Phenethyl alcohol; b-Phenylethyl alcohol; (3-endo)-8-Azabicyclo[3.2.1]octan-3-olato(2-) hydrochloride (1:1); endo-8-Azabicyclo[3.2.1]octan-3-ol; nortropan-3endo-ol; N-Demethyltropine; PEA; N-normethyltropine; Benzeneethanol; Phenyl Ethanol; Q2R; 3-hydroxy-nortropan; NOR-TROPANOL |
| Molecular Formula | C7H13O1N1 |
| Molecular Weight | 127.19 |
| Purity | 99 |
| Density | 1.0±0.1 g/cm3 |
| Boiling Point | 218.2±8.0 °C at 760 mmHg |
| Melting Point | 108-110ºC |
| Appearance | light yellowish brown solid |
| Storage Condition | Room temperature, sealed, dry |
| Application | Nortropine (Nortropenol) can be isolated from Convolvulus subhirsutus alkaloids and is an intermediate in the decomposition and reaction of tropine base to produce succinic acid. |
| HTC | 2933990090 |
| MDL Number | MFCD00047140 |
| SMILES | OC1CC2CCC(C1)N2 |
| InChI | InChI=1S/C7H13NO/c9-7-3-5-1-2-6(4-7)8-5/h5-9H,1-4H2 |
| InChI Key | YYMCYJLIYNNOMK-MEKDEQNOSA-N |
| MSDS | msds/11717_1_538_09_0.pdf |
| Bioactivity | Nortropine (Nortropenol), isolated from the total alkaloids of Convolvulus subhirsutus, is an intermediate in tropine breakdown and reactions leading to succinate[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Bartholomew BA, et al. Atropine Metabolism by Pseudomonas sp. Strain AT3: Evidence for Nortropine as an Intermediate in Tropine Breakdown and Reactions Leading to Succinate. Appl Environ Microbiol. 1996 Sep;62(9):3245-50. [2]. A. M. Gapparov, et al. Alkaloids of Convolvulus subhirsutus from Uzbekistan. Chemistry of Natural Compounds. 2007. 43(3):291-292. Chemical & Physical Properties Density 1.0±0.1 g/cm3 Boiling Point 218.2±8.0 °C at 760 mmHg Melting Point 108-110ºC Molecular Formula C7H13NO Molecular Weight 122.164 Flash Point 102.2±0.0 °C Exact Mass 122.073166 PSA 40.46000 LogP 1.36 Vapour Pressure 0.1±0.5 mmHg at 25°C Index of Refraction 1.536 InChIKey YYMCYJLIYNNOMK-MEKDEQNOSA-N SMILES OC1CC2CCC(C1)N2 |
| Use of | Nortropine (Nortropenol), isolated from the total alkaloids of Convolvulus subhirsutus, is an intermediate in tropine breakdown and reactions leading to succinate[1]. Properties Name Nortropine Synonym More Synonyms 8-Aza-bicyclo[3.2.1]octan-3-ol HCl Biological Activity Description Nortropine (Nortropenol), isolated from the total alkaloids of Convolvulus subhirsutus, is an intermediate in tropine breakdown and reactions leading to succinate[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Bartholomew BA, et al. Atropine Metabolism by Pseudomonas sp. Strain AT3: Evidence for Nortropine as an Intermediate in Tropine Breakdown and Reactions Leading to Succinate. Appl Environ Microbiol. 1996 Sep;62(9):3245-50. [2]. A. M. Gapparov, et al. Alkaloids of Convolvulus subhirsutus from Uzbekistan. Chemistry of Natural Compounds. 2007. 43(3):291-292. Chemical & Physical Properties Molecular Formula C7H13NO Exact Mass 122.073166 PSA 40.46000 Index of Refraction 1.536 InChIKey YYMCYJLIYNNOMK-MEKDEQNOSA-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 United Nations classification: inconsistent with United Nations classification standards UN number: not specified Nortropinol Modification Number: 5 |
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