CAS Number204251-24-1
SynonymsFmoc-L-GlutamicacidmonohydrateO-t-butylester; FMOC-L-GLUTAMIC ACID (OTBU) MONOHYDRATE; FMOC-L-GLU(OTBU)-OH H2O; FMOC-L-GLUTAMIC ACID-O-T-BUTYL ESTER MONOHYDRATE; FMOC-L-GLU(TBU)-OH H2O; FMOC-L-Glutamic acid-O-tert-butyl ester monohydrate; FMOC-GLUTAMIC ACID(OTBU)-OH H2O; L-Glutamic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 5-(1,1-dimethylethyl) ester, hydrate (1:1); Fmoc-L-Glu(otbu)-OH hydrate; FMOC-GLU(OBUT) H2O; (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid hydrate; Fmoc-L-Glutamic acid-O-tert-butyl ester hydrate; MFCD00150485
Molecular FormulaC24H29NO7
Molecular Weight443.490
Purity98.00%
Boiling Point633.5ºC at 760mmHg
Melting Point89-93ºC
AppearanceWhite fine powder
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 204251-24-1 |
| Catalog No. | 2A-9055304 |
| Chinese Name | N-(9-芴基甲氧羰基)-L-谷氨酸-GAMMA-叔丁基 酯 |
| Synonyms | Fmoc-L-GlutamicacidmonohydrateO-t-butylester; FMOC-L-GLUTAMIC ACID (OTBU) MONOHYDRATE; FMOC-L-GLU(OTBU)-OH H2O; FMOC-L-GLUTAMIC ACID-O-T-BUTYL ESTER MONOHYDRATE; FMOC-L-GLU(TBU)-OH H2O; FMOC-L-Glutamic acid-O-tert-butyl ester monohydrate; FMOC-GLUTAMIC ACID(OTBU)-OH H2O; L-Glutamic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 5-(1,1-dimethylethyl) ester, hydrate (1:1); Fmoc-L-Glu(otbu)-OH hydrate; FMOC-GLU(OBUT) H2O; (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid hydrate; Fmoc-L-Glutamic acid-O-tert-butyl ester hydrate; MFCD00150485 |
| Molecular Formula | C24H29NO7 |
| Molecular Weight | 443.490 |
| Purity | 98.00 |
| Boiling Point | 633.5ºC at 760mmHg |
| Melting Point | 89-93ºC |
| Appearance | White fine powder |
| Storage Condition | Sealed in a cool, dry environment at -20 ºC |
| Application | (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentaenoic acid hydrate is a glutamic acid derivative [1]. |
| SMILES | CC(C)(C)OC(=O)CCC(NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O.O |
| InChI | InChI=1S/C24H27NO6/c1-24(2,3)31-21(26)13-12-20(22(27)28)25-23(29)30-14-19-17-10-6-4-8-15(17)16-9-5-7-11-18(16)19/h4-11,19-20H,12-14H2,1-3H3,(H,25,29)(H,27,28)/p-1/t20-/m0/s1 |
| InChI Key | NMBGBVUJSPZRDD-BDQAORGHSA-N |
| Hazard Symbols | transportation |
| MSDS | msds/55304_2_204251_24_1.pdf |
| Bioactivity | (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid hydrate is a glutamic acid 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 Boiling Point 633.5ºC at 760mmHg Melting Point 89-93ºC Molecular Formula C24H29NO7 Molecular Weight 443.490 Flash Point 336.9ºC Exact Mass 443.194397 PSA 111.16000 LogP 4.42680 Vapour Pressure 6.39E-17mmHg at 25°C InChIKey NMBGBVUJSPZRDD-BDQAORGHSA-N SMILES CC(C)(C)OC(=O)CCC(NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O.O Storage condition -20°C |
| Use of | (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid hydrate is a glutamic acid derivative[1]. Properties Name fmoc-glu(otbu)-oh h2o Synonym More Synonyms Biological Activity Description (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid hydrate is a glutamic acid 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 C24H29NO7 Exact Mass 443.194397 PSA 111.16000 LogP 4.42680 InChIKey NMBGBVUJSPZRDD-BDQAORGHSA-N |
| Transport Info | Shipping Name: UN |
| 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 United Nations shipping name 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 Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available |
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