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CIS-9,10-METHYLENEHEXADECANOIC ACID, also known as Cis-9,10-methylenehexadecanoic acid, is a unique saturated fatty acid with the chemical formula C17H32O2. It features a distinctive methylene group between the ninth and tenth carbon atoms, which distinguishes it from other fatty acids. Naturally occurring in some animal and plant sources, CIS-9,10-METHYLENEHEXADECANOIC ACID is also synthesized for a variety of applications in industry and science. Research has highlighted its potential therapeutic properties, such as its capacity to influence lipid metabolism and inflammatory responses, and it is being explored for the development of pharmaceuticals and bio-based materials.

4675-60-9

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4675-60-9 Usage

Uses

Used in Pharmaceutical Development:
CIS-9,10-METHYLENEHEXADECANOIC ACID is used as a key component in the development of new pharmaceuticals for its potential to modulate lipid metabolism and inflammatory processes. Its unique structure may offer novel therapeutic avenues for treating various diseases and conditions.
Used in Bio-based Material Production:
In the industry of bio-based materials, CIS-9,10-METHYLENEHEXADECANOIC ACID is utilized as a building block for creating sustainable and eco-friendly materials. Its chemical properties make it a promising candidate for the development of innovative products that can replace petroleum-based counterparts.
Used in Scientific Research:
CIS-9,10-METHYLENEHEXADECANOIC ACID serves as an important subject of study in scientific research, where it is investigated for its potential applications in modulating biological processes. Understanding its interactions with biological systems can lead to advancements in medicine and other fields.
Used in Nutritional Supplements:
Given its role in lipid metabolism, CIS-9,10-METHYLENEHEXADECANOIC ACID may be used as an ingredient in nutritional supplements designed to support healthy lipid profiles and overall metabolic function.
Used in Cosmetics and Personal Care:
In the cosmetics and personal care industry, CIS-9,10-METHYLENEHEXADECANOIC ACID could be employed for its potential benefits to skin health, possibly improving the texture and appearance of the skin due to its influence on lipid metabolism.

Check Digit Verification of cas no

The CAS Registry Mumber 4675-60-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,7 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4675-60:
(6*4)+(5*6)+(4*7)+(3*5)+(2*6)+(1*0)=109
109 % 10 = 9
So 4675-60-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H32O2/c1-2-3-4-8-11-15-14-16(15)12-9-6-5-7-10-13-17(18)19/h15-16H,2-14H2,1H3,(H,18,19)

4675-60-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-[(1S,2R)-2-hexylcyclopropyl]octanoic acid

1.2 Other means of identification

Product number -
Other names Cyclopropaneoctanoic acid,2-hexyl-,cis

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4675-60-9 SDS

4675-60-9Downstream Products

4675-60-9Relevant academic research and scientific papers

Ascaroside Signaling in the Bacterivorous Nematode Caenorhabditis remanei Encodes the Growth Phase of Its Bacterial Food Source

Dolke, Franziska,Dong, Chuanfu,Bandi, Siva,Paetz, Christian,Glauser, Gaétan,Von Reu?, Stephan H.

, p. 5832 - 5837 (2019/08/26)

A novel class of species-specific modular ascarosides that integrate additional fatty acid building blocks was characterized in the nematode Caenorhabditis remanei using a combination of HPLC-ESI-(-)-MS/MS precursor ion scanning, microreactions, HR-MS/MS, MSn, and NMR techniques. The structure of the dominating component carrying a cyclopropyl fatty acid moiety was established by total synthesis. Biogenesis of this female-produced male attractant depends on cyclopropyl fatty acid synthase (cfa), which is expressed in bacteria upon entering their stationary phase.

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