79728-54-4 Usage
General Description
10-hydroxy-8-decenoic acid, also known as 10-HDA, is a unique fatty acid found in royal jelly, a substance produced by honeybees. It has been identified as one of the major bioactive components responsible for the many health benefits of royal jelly. 10-HDA has been shown to have anti-inflammatory, antioxidant, and anti-cancer properties, making it a popular ingredient in various health and skincare products. In addition to its potential therapeutic effects, 10-HDA also plays a crucial role in the growth and development of queen bees, highlighting its importance in the bee colony. Studies suggest that 10-HDA may have potential applications in medical and cosmetic research due to its versatile biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 79728-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,2 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79728-54:
(7*7)+(6*9)+(5*7)+(4*2)+(3*8)+(2*5)+(1*4)=184
184 % 10 = 4
So 79728-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O3/c11-9-7-5-3-1-2-4-6-8-10(12)13/h5,7,11H,1-4,6,8-9H2,(H,12,13)/b7-5+
79728-54-4Relevant articles and documents
(8E)-10-Hydroxydec-8-enoic Acid: its Isolation from Injured Fruit Bodies of Cantharellus tubaeformis and Synthetic Preparation
Pang, Zijie,Sterner, Olov,Anke, Heidrun
, p. 301 - 303 (2007/10/02)
The chemical contents of both intact and injured fruit bodies of the edible mushroom Cantharellus tubaeformis have been investigated and compared with those of C. cibarius (chanterelle).Ethyl acetate extracts of intact fruit bodies of the two species were found to contain the same major components, but extracts of injured fruit bodies differ with respect to two metabolites.No traces of cibaric acid, formed enzymatically in injured fruit bodies of C. cibarius, could be detected in the fruit bodies of C. tubaeformis, which instead forms (8E)-10-hydroxy-8-decenoic acid in response to injury.The structure of (8E)-10-hydroxy-8-decenoic acid was elucidated by spectroscopic methods, and confirmed by synthesis.
