24607-05-4

Basic information

• Product Name: Heptadecane-16-yne-1,2,4-triol
• Synonyms: 16-Heptadecyne-1,2,4-triol;Avocadyne;Heptadecane-16-yne-1,2,4-triol
• CAS NO: 24607-05-4
• Molecular Formula: C₁₇H₃₂O₃
• Molecular Weight: 0
• Mol File: 24607-05-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 443°C at 760 mmHg
• Flash Point: 198.6°C
• Appearance: /
• Density: 0.993g/cm³
• Vapor Pressure: 1.04E-09mmHg at 25°C
• Refractive Index: 1.492
• CAS DataBase Reference: Heptadecane-16-yne-1,2,4-triol(CAS DataBase Reference)
• NIST Chemistry Reference: Heptadecane-16-yne-1,2,4-triol(24607-05-4)
• EPA Substance Registry System: Heptadecane-16-yne-1,2,4-triol(24607-05-4)

Safety Data

• Hazardous Substances Data: 24607-05-4(Hazardous Substances Data)

Usage

Uses

Avocadyne is an anti fungal compound found in immature avocado peel and seeds.

InChI:InChI=1/C17H32O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-16(19)14-17(20)15-18/h1,16-20H,3-15H2

Upstream product

• 52056-69-6 2-[(11-bromoundecyl)oxy]tetrahydro-2H-pyran 
• 56772-54-4 13-<(tetrahydropyran-2'-yl)oxy>tridecan-1-yne 
• 1611-56-9 1-Bromo-11-hydroxyundecane 
• 4282-44-4 1-iodo-n-undecane 
• 129014-19-3 (2R,4RS) 1,2-acetonide-17-trimethylsilyl-16-heptadecyn-1,2,4-triol 
• 129014-21-7 trimethyl-(13-((tetrahydro-2H-pyran-2-yl)oxy)tridec-1-yn-1-yl)silane 
• 129014-23-9 (13-bromotridec-1-ynyl)trimethylsilane 
• 129014-22-8 13-trimethylsilyl-12-tridecyn-1-ol 
• 129014-20-6 (2R,4RS) 1,2-acetonide-16-heptadecyn-1,2,4-triol 
• 24607-06-5 avocadyne acetate 

Downstream Products

• 83797-45-9 1,2,4-trihydroxy-heptadeca-16-ene 
• 24607-08-7 avocadene 

Relevant articles and documents

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THE ABSOLUTE CONFIGURATION EFFECT ON THE ACTIVITY OF THE AVOCADO ROOTING PROMOTER

16-Heptadecyn-1,2,4-triol is the most active component of the avocado rooting promotor (ARP).All four diastereoisomers of this compound have been synthesized.Their root promoting activity was determined over the physiologically active concentration range.It was found that the (2R,4R)-stereoisomer exerts a rooting activity similar to that of the extracted and purified compound from avocado tissues.The (2R,4S), and (2S,4R)-stereoisomers had lower activity and the (2S,4S)-stereoisomer had the lowest activity.It is concluded that the natural form, (2R,4R), acts in the rooting process either in its original structure or after reaction which does not alter its chiral centres.