CAS Number34582-32-6
SynonymsMFCD00038272; 1-tert-Butyl N-(tert-Butoxycarbonyl)-L-aspartate; |A-tert-Butyl-N-Boc-L-aspartate; FC1234; Boc-ASp-OtBu; N-(tert-Butoxycarbonyl)-L-aspartic Acid 1-tert-Butyl Ester; Boc-L-Aspartic acid 1-tert-butyl ester; Boc-L-Asp-OtBu; L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(1,1-dimethylethyl) ester; (3S)-4-[(2-Methyl-2-propanyl)oxy]-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid; ASP002; N-Boc-L-aspartic Acid 1-tert-Butyl Ester; 1-tert-Butyl N-Boc-L-aspartate; (3S)-4-tert-Butoxy-3-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name)
Molecular FormulaC13H23NO6
Molecular Weight289.32
Purity≥98 (TLC)%
Density1.1±0.1 g/cm3
Boiling Point429.0±40.0 °C at 760 mmHg
Melting Point101-103?C
Appearancepowder
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 34582-32-6 |
| Catalog No. | 2A-9007268 |
| Chinese Name | N-叔丁氧羰基-L-天冬氨酸 1-叔丁酯 |
| Synonyms | MFCD00038272; 1-tert-Butyl N-(tert-Butoxycarbonyl)-L-aspartate; |A-tert-Butyl-N-Boc-L-aspartate; FC1234; Boc-ASp-OtBu; N-(tert-Butoxycarbonyl)-L-aspartic Acid 1-tert-Butyl Ester; Boc-L-Aspartic acid 1-tert-butyl ester; Boc-L-Asp-OtBu; L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(1,1-dimethylethyl) ester; (3S)-4-[(2-Methyl-2-propanyl)oxy]-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid; ASP002; N-Boc-L-aspartic Acid 1-tert-Butyl Ester; 1-tert-Butyl N-Boc-L-aspartate; (3S)-4-tert-Butoxy-3-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name) |
| Molecular Formula | C13H23NO6 |
| Molecular Weight | 289.32 |
| Purity | ≥98 (TLC) |
| Density | 1.1±0.1 g/cm3 |
| Boiling Point | 429.0±40.0 °C at 760 mmHg |
| Melting Point | 101-103?C |
| Appearance | powder |
| Water Solubility | Soluble in: methanol |
| Storage Condition | Seal and store at -15ºC |
| Application | (S)-4-(tert-butoxy)-3-((tert-butoxycarbonyl)amino)-4-oxobutyric acid is an aspartic acid derivative [1]. |
| HTC | 2924.19.8000 |
| UN(IATA) | NA |
| MDL Number | MFCD00038272 |
| SMILES | N([C@@H](CC(=O)O)C(=O)OC(C)(C)C)C(=O)OC(C)(C)C |
| InChI | 1S/C13H23NO6/c1-12(2,3)19-10(17)8(7-9(15)16)14-11(18)20-13(4,5)6/h8H,7H2,1-6H3,(H,14,18)(H,15,16)/t8-/m0/s1 |
| InChI Key | RAUQRYTYJIYLTF-QMMMGPOBSA-N |
| NACRES Code | NA.22 |
| UNSPSC | 12352209 |
| Hazard Symbols | Transport |
| MSDS | msds/7268_1_34582_32_6.pdf |
| Bioactivity | (S)-4-(tert-Butoxy)-3-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid is an aspartic 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 Density 1.1±0.1 g/cm3 Boiling Point 429.0±40.0 °C at 760 mmHg Melting Point 101-103?C Molecular Formula C13H23NO6 Molecular Weight 289.325 Flash Point 213.3±27.3 °C Exact Mass 289.152527 PSA 101.93000 LogP 2.72 Vapour Pressure 0.0±2.2 mmHg at 25°C Index of Refraction 1.470 InChIKey RAUQRYTYJIYLTF-QMMMGPOBSA-N SMILES CC(C)(C)OC(=O)NC(CC(=O)O)C(=O)OC(C)(C)C Storage condition -15°C |
| Use of | (S)-4-(tert-Butoxy)-3-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid is an aspartic acid derivative[1]. Properties Name (3S)-4-[(2-methylpropan-2-yl)oxy]-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoic acid Synonym More Synonyms Boc-Asp-OtBu Biological Activity Description (S)-4-(tert-Butoxy)-3-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid is an aspartic 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 C13H23NO6 Exact Mass 289.152527 PSA 101.93000 Index of Refraction 1.470 InChIKey RAUQRYTYJIYLTF-QMMMGPOBSA-N SMILES CC(C)(C)OC(=O)NC(CC(=O)O)C(=O)OC(C)(C)C |
| 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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