1H-1,2,4-Triazole-5-propanoicacid, a-amino-
1H-1,2,4-Triazole-5-propanoicacid, a-amino- structure
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Common Name | 1H-1,2,4-Triazole-5-propanoicacid, a-amino- | ||
|---|---|---|---|---|
| CAS Number | 10109-05-4 | Molecular Weight | 156.14300 | |
| Density | 1.527g/cm3 | Boiling Point | 454.1ºC at 760mmHg | |
| Molecular Formula | C5H8N4O2 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 228.4ºC | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of 1H-1,2,4-Triazole-5-propanoicacid, a-amino-β-(1,2,4-Triazol-3-yl)-DL-alanine is an alanine derivative[1]. |
| Name | triazolealanine |
|---|---|
| Synonym | More Synonyms |
| Description | β-(1,2,4-Triazol-3-yl)-DL-alanine is an alanine derivative[1]. |
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| Related Catalog | |
| 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 |
| Density | 1.527g/cm3 |
|---|---|
| Boiling Point | 454.1ºC at 760mmHg |
| Molecular Formula | C5H8N4O2 |
| Molecular Weight | 156.14300 |
| Flash Point | 228.4ºC |
| Exact Mass | 156.06500 |
| PSA | 104.89000 |
| Vapour Pressure | 4.9E-09mmHg at 25°C |
| Index of Refraction | 1.624 |
| Storage condition | −20°C |
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302 |
| Hazard Codes | Xi: Irritant; |
| Risk Phrases | 36/37/38 |
| Safety Phrases | 26-36 |
| RIDADR | NONH for all modes of transport |
| HS Code | 2933990090 |
| HS Code | 2933990090 |
|---|---|
| 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% |
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Incorporation of amino acid analogs during the biosynthesis of Escherichia coli aspartate transcarbamylase.
Biochim. Biophys. Acta 615(1) , 59-69, (1980) Amino acid-requiring mutants capable of producing derepressed levels of aspartate transcarbamylase (carbamoylphosphate:L-aspartate carbamoyltransferase, EC 2.1.3.2) were obtained and used for the inco... |
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Synthesis of a novel histidine analogue and its efficient incorporation into a protein in vivo.
Protein Eng. 16 , 699-706, (2003) Proteins containing unnatural amino acids have immense potential in biotechnology and medicine. We prepared several histidine analogues including a novel histidine analogue, beta-(1,2,3-triazol-4-yl)-... |
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Classifying mutagens as to their specificity in causing the six possible transitions and transversions: a simple analysis using the Salmonella mutagenicity assay.
Environ. Mutagen. 8 , 9, (1986) The standard Salmonella tester strains used to detect base substitution mutations carry the hisG428 ochre mutation (TA102 and TA104) and the hisG46 missense mutation (TA100). These mutations can be re... |
| 2-amino-3-(1H-[1,2,4]triazol-3-yl)-propionic acid |
| 2-amino-3-(1H-1,2,4-triazol-5-yl)propanoic acid |
| EINECS 233-301-2 |
| 3-(4h-1,2,4-triazol-3-yl)alanine |
| 1,2,4-Triazole-3-alanine |
| 2-Amino-3-(1H-[1,2,4]triazol-3-yl)-propionsaeure |
| Triazolealanine |
| 3-(1,2,4-triazol-3-yl)-D,L-alanine |