Identification | More | [Name]
4-PENTYNOIC ACID | [CAS]
6089-09-4 | [Synonyms]
4-PENTYNOIC ACID PROPARGYLACETIC ACID TIMTEC-BB SBB009121 Pent-4-yn-1-oic acid pent-4-yn-1-oicacid 4-Pentynoicacid,98% Pentane-4-ynoic acid | [EINECS(EC#)]
228-028-0 | [Molecular Formula]
C5H6O2 | [MDL Number]
MFCD00004407 | [Molecular Weight]
98.1 | [MOL File]
6089-09-4.mol |
Chemical Properties | Back Directory | [Appearance]
white to beige crystalline powder or flakes | [Melting point ]
54-57 °C(lit.)
| [Boiling point ]
110 °C30 mm Hg(lit.)
| [density ]
1.1133 (rough estimate) | [refractive index ]
1.3930 (estimate) | [Fp ]
75 °C
| [storage temp. ]
2-8°C
| [form ]
Crystalline Powder or Flakes | [pka]
4.30±0.10(Predicted) | [color ]
White to beige | [Water Solubility ]
Soluble in low polarity organic solvents. Soluble in water. | [Sensitive ]
Light & Air Sensitive & Hygroscopic | [BRN ]
1742047 | [InChIKey]
MLBYLEUJXUBIJJ-UHFFFAOYSA-N | [LogP]
0.402 (est) | [CAS DataBase Reference]
6089-09-4(CAS DataBase Reference) | [Storage Precautions]
Air sensitive;Store under nitrogen;Light sensitive |
Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R34:Causes burns. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
UN 3261 8/PG 2
| [WGK Germany ]
3
| [RTECS ]
SC4751000
| [F ]
8-10-23 | [Hazard Note ]
Corrosive | [HazardClass ]
8 | [PackingGroup ]
III | [HS Code ]
29161900 |
Hazard Information | Back Directory | [Chemical Properties]
white to beige crystalline powder or flakes | [Uses]
4-Pentynoic Acid is a hypoglycemic agent shown to increase liver tyrosine aminotransferase and plasma corticosterone while decreasing blood sugar in rats. | [General Description]
4-Pentynoic acid undergoes copper-catalyzed intramolecular cyclizations to form enol lactones. It also reacts with 1-bromo-1-alkynes in the presence of a Pd catalyst to yield biologically active ynenol lactones. |
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