CAS Number86069-86-5
Synonymsfmoc-l-pipecolic acid; MFCD00235898; 2,2-Piperidinedicarboxylic acid, 2-(9H-fluoren-9-ylmethyl) ester; (2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecarboxylic acid; (2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]piperidine-2-carboxylic acid; 2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecarboxylic acid; Fmoc-β-Homo-Pro-OH; (S)-1-FMOC-PIPERIDINE-2-CARBOXYLIC ACID; Fmoc-HomoPro-OH; N-Fmoc-L-pipecolic acid; (S)-1,2-Piperidinedicarboxylic acid 1-(9H-fluoren-9-ylmethyl) ester; Fmoc-HoPro-OH
Molecular FormulaC21H21NO4
Molecular Weight351.40
Purity97%
Density1.293±0.06 g/cm3
Boiling Point553.7±50.0 °C at 760 mmHg
Melting Point153-158 °C
Appearancepowder
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 86069-86-5 |
| Catalog No. | 2A-9000144 |
| Chinese Name | N-Fmoc-L-哌啶酸 |
| Synonyms | fmoc-l-pipecolic acid; MFCD00235898; 2,2-Piperidinedicarboxylic acid, 2-(9H-fluoren-9-ylmethyl) ester; (2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecarboxylic acid; (2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]piperidine-2-carboxylic acid; 2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecarboxylic acid; Fmoc-β-Homo-Pro-OH; (S)-1-FMOC-PIPERIDINE-2-CARBOXYLIC ACID; Fmoc-HomoPro-OH; N-Fmoc-L-pipecolic acid; (S)-1,2-Piperidinedicarboxylic acid 1-(9H-fluoren-9-ylmethyl) ester; Fmoc-HoPro-OH |
| Molecular Formula | C21H21NO4 |
| Molecular Weight | 351.40 |
| Purity | 97 |
| Density | 1.293±0.06 g/cm3 |
| Boiling Point | 553.7±50.0 °C at 760 mmHg |
| Melting Point | 153-158 °C |
| Appearance | powder |
| Water Solubility | Insuluble (8.8E-3 g/L) (25 ºC) |
| Storage Condition | Refrigerated and sealed at 2-8°C, in nitrogen |
| Application | Fmoc HoPro OH is a proline derivative [1]. |
| HTC | 2933399090 |
| UN(IATA) | UN 3077 9/PG 3 |
| PubChem ID | 329762639 |
| MDL Number | MFCD00235898 |
| SMILES | OC(=O)[C@@H]1CCCCN1C(=O)OCC2c3ccccc3-c4ccccc24 |
| InChI | 1S/C21H21NO4/c23-20(24)19-11-5-6-12-22(19)21(25)26-13-18-16-9-3-1-7-14(16)15-8-2-4-10-17(15)18/h1-4,7-10,18-19H,5-6,11-13H2,(H,23,24)/t19-/m0/s1 |
| InChI Key | CKLAZLINARHOTG-IBGZPJMESA-N |
| Beilstein/REAXYS | 4718405 |
| NACRES Code | NA.26 |
| UNSPSC | 12352106 |
| Hazard Symbols | Transport |
| Risk Codes | 50/53 |
| Safety Description | 60-61 |
| MSDS | msds/144_1_86069_86_5.pdf |
| Bioactivity | Fmoc-HoPro-OH is a proline derivative[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. References [1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. Chemical & Physical Properties Density 1.293±0.06 g/cm3 Boiling Point 553.7±50.0 °C at 760 mmHg Melting Point 161-162.5 ºC Molecular Formula C21H21NO4 Molecular Weight 351.396 Flash Point 288.7±30.1 °C Exact Mass 351.147064 PSA 66.84000 LogP 3.92 Vapour Pressure 0.0±1.6 mmHg at 25°C Index of Refraction 1.608 InChIKey CKLAZLINARHOTG-IBGZPJMESA-N SMILES O=C(O)C1CCCCN1C(=O)OCC1c2ccccc2-c2ccccc21 Storage condition 2-8°C Water Solubility Insuluble (8.8E-3 g/L) (25 ºC) |
| Use of | Fmoc-HoPro-OH is a proline derivative[1]. Properties Name Fmoc-(S)-(-)-piperidine-2-carboxylic acid Synonym More Synonyms N-Fmoc-L-pipecolic acid Biological Activity Description Fmoc-HoPro-OH is a proline derivative[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. References [1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. Chemical & Physical Properties Molecular Formula C21H21NO4 Exact Mass 351.147064 PSA 66.84000 Index of Refraction 1.608 InChIKey CKLAZLINARHOTG-IBGZPJMESA-N |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 20.0% |
| Transport Info | Shipping Name: UN |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Danger Regulations: 3077 International Maritime Transport Danger Regulations: 3077 International Air Transport Danger Regulations: 3077 14.2 United Nations shipping name European land transport hazard regulations: ENVIRONMENTALLY HAZARDOUS SUBSTANCE, SOLID, N.O.S. ((S)-N-Fmoc- piperidine-2-carboxylic acid) IMDG Code: ENVIRONMENTALLY HAZARDOUS SUBSTANCE, SOLID, N.O.S. ((S)-N-Fmoc- piperidine-2-carboxylic acid) International air transport hazard regulations: Environmentally hazardous substance, solid, n.o.s. ((S)-N-Fmoc-piperidine-2-carboxylic acid) 14.3 Transport hazard categories European land transport Dangerous Regulations: 9 International sea transport Dangerous Regulations: 9 International air transport Dangerous Regulations: 9 14.4 Package group European Land Transport Danger Regulations: III International Maritime Transport Danger Regulations: III International Air Transport Danger Regulations: III 14.5 Environmental hazards European Land Transport Dangerous Regulations: Yes International Maritime Transport Dangerous Regulations International Air Transport Dangerous Regulations: Yes Marine Pollutants (Yes/No): Yes 14.6 Special reminder to users further information Dangerous goods are individually packaged, with liquids exceeding 5 liters or solids exceeding 5 kilograms. The outer packaging of each independent package and the combined independent inner package must have EHS on it. Identification (according to European ADR Regulation 2.2.9.1.10, IMDG Regulation 2.10.3), |
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