Introduction：Basic information about CAS 3128-06-1|Glurate, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Glurate |
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| CAS Number | 3128-06-1 | Molecular Weight | 130.14200 |
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| Density | 1.09 g/mL at 25 °C(lit.) | Boiling Point | 274-275 °C(lit.) |
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| Molecular Formula | C6H10O3 | Melting Point | 13-14 °C(lit.) |
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| MSDS | ChineseUSA | Flash Point | >230 °F |
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Names
| Name | 5-oxohexanoic acid |
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| Synonym | More Synonyms |
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Glurate BiologicalActivity
| Description | Glurate (4-Acetylbutyric acid; 5-Oxohexanoic acid) can be used to construct antiviral agents (acyclic nucleoside esters) (extracted from patent WO1997030052A1)[1]. |
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| Related Catalog | Research Areas >>InfectionSignaling Pathways >>Others >>Others |
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| References | [1]. Per Engelhardt, et al. Synthesis of acyclic nucleosides. Patent WO1997030052A1. |
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Chemical & Physical Properties
| Density | 1.09 g/mL at 25 °C(lit.) |
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| Boiling Point | 274-275 °C(lit.) |
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| Melting Point | 13-14 °C(lit.) |
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| Molecular Formula | C6H10O3 |
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| Molecular Weight | 130.14200 |
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| Flash Point | >230 °F |
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| Exact Mass | 130.06300 |
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| PSA | 54.37000 |
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| LogP | 0.83030 |
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| Index of Refraction | n20/D 1.4451(lit.) |
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Safety Information
| Personal Protective Equipment | Eyeshields;Gloves |
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| Risk Phrases | R36/38 |
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| Safety Phrases | S26-S36 |
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| RIDADR | NONH for all modes of transport |
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| WGK Germany | 3 |
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| HS Code | 2918300090 |
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Customs
| HS Code | 2918300090 |
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| Summary | 2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0% |
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Articles5
More Articles
| Identification of 5-hydroxyhexanoic acid, 4-hydroxyheptanoic acid and 4-hydroxyoctanoic acid as new constituents of bacterial polyhydroxyalkanoic acids. Valentin HE, et al. Appl. Microbiol. Biotechnol. 46(3) , 261-267, (1996)
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| Proline-like β-turn mimics accessed via Ugi reaction involving monoprotected hydrazines. Krasavin M, et al. Tetrahedron Lett. 51(10) , 1367-70, (2010)
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| A versatile and concise route to functionally substituted ?-butyrolactones and spiro-XXX-butyrolactones (lactone annelation) Mandal AK and Jawalkar DG Tetrahedron Lett. 27.1 , 99-100, (1986)
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Synonyms
| EINECS 221-511-7 |
| 5-Ketocaproic acid |
| 5-Oxohexanoic Acid |
| 4-Acetylbutyric Acid |
| 4-Acetylbutyricacid |
| 5-Ketohexanoic acid |
| Hexanoic acid,5-oxo |
| 5-oxocaproic acid |
| 4-acetyl-butanoic acid |
| MFCD00004412 |
| 5-oxo-hexanoic acid |
