4-Pentenoic acid
CAS No. 591-80-0
4-Pentenoic acid ( —— )
Catalog No. M21389 CAS No. 591-80-0
4-Pentenoic acid also known as allyl acetic acid or 4-pentenate belongs to the class of organic compounds known as straight chain fatty acids. These are fatty acids with a straight aliphatic chain. 4-Pentenoic acid is a very hydrophobic molecule practically insoluble (in water) and relatively neutral.
Purity : >98% (HPLC)
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Biological Information
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Product Name4-Pentenoic acid
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NoteResearch use only not for human use.
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Brief Description4-Pentenoic acid also known as allyl acetic acid or 4-pentenate belongs to the class of organic compounds known as straight chain fatty acids. These are fatty acids with a straight aliphatic chain. 4-Pentenoic acid is a very hydrophobic molecule practically insoluble (in water) and relatively neutral.
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Description4-Pentenoic acid also known as allyl acetic acid or 4-pentenate belongs to the class of organic compounds known as straight chain fatty acids. These are fatty acids with a straight aliphatic chain. 4-Pentenoic acid is a very hydrophobic molecule practically insoluble (in water) and relatively neutral.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number591-80-0
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Formula Weight100.12
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Molecular FormulaC5H8O2
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Purity>98% (HPLC)
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Solubility——
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SMILESOC(=O)CCC=C
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Ricinine
Ricinine is a major alkaloid in Ricinus communis plant with hepatoprotection in CCl4 -induced liver damage.
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3-Phenyl-2-propen-1-...
The compounds 3-phenyl-2-propen-1-ol , 2-methyl-3-butyn-2-ol, 3,7-dimethylnonane, and 2-hydroxybenzoic acid occurred only during estrus which may be considered as marker for detection of estrus which would ultimately help for artificial insemination in captive condition.
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N-Acetyl-L-phenylala...
N-Acetyl-L-phenylalanine is an essential amino acid produced for medical feed and nutritional applications. It appears in large amount in urine of patients with phenylketonuria which is a human genetic disorder due to the lack of phenylalanine hydroxylase the enzyme necessary to metabolize phenylalanine to tyrosine.