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N-(2-hydroxyethyl)docosanamide is a saturated N-acylethanolamide, a type of endocannabinoid that plays a role in various physiological processes. It is structurally similar to docosanoyl ethanolamide, but with an additional hydroxyethyl group. The non-cannabinoid receptor-mediated pharmacology of N-(2-hydroxyethyl)docosanamide is still being studied, and it may have potential applications in various fields.

94109-05-4

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94109-05-4 Usage

Uses

Used in Pharmaceutical Industry:
N-(2-hydroxyethyl)docosanamide is used as a potential therapeutic agent for various conditions due to its endocannabinoid-like properties. It may have potential applications in the treatment of memory disorders, weight loss and appetite regulation, neurodegeneration, tumor surveillance, analgesia, and inflammation.
Used in Research:
N-(2-hydroxyethyl)docosanamide is used as a research compound to study the non-cannabinoid receptor-mediated pharmacology of saturated N-acylethanolamides. This can help in understanding their role in the functioning of ion channels and other physiological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 94109-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,0 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94109-05:
(7*9)+(6*4)+(5*1)+(4*0)+(3*9)+(2*0)+(1*5)=124
124 % 10 = 4
So 94109-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C24H49NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-24(27)25-22-23-26/h26H,2-23H2,1H3,(H,25,27)

94109-05-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-hydroxyethyl)docosanamide

1.2 Other means of identification

Product number -
Other names Behenoyl monoethanolamide

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:94109-05-4 SDS

94109-05-4Upstream product

94109-05-4Downstream Products

94109-05-4Relevant academic research and scientific papers

Synthesis and anticonvulsant activity of N-(2-hydroxyethyl)amide derivatives

Guan, Li-Ping,Zhao, Dong-Hai,Xiu, Jing-Hui,Sui, Xin,Piao, Hu-Ri,Quan, Zhe-Shan

, p. 34 - 40 (2009)

A series novel of N-(2-hydroxyethyl)amide derivatives was synthesized and screened for their anticonvulsant activities by the maximal electroshock (MES) test, and their neurotoxicity was evaluated by the rotarod test (Tox). The maximal electroshock test showed that N-(2-hydroxyethyl)decanamide 1g, N-(2-hydroxyethyl)palmitamide 1l, and N-(2-hydroxyeth-yl)stearamide 1n were found to show a better anticonvulsant activity and also had lower toxicity than the marked anti-epileptic drug valproate. In the anti-MES potency test, these compounds exhibited median effective doses (ED50) of 22.0, 23.3, 20.5 mg/kg, respectively, and median toxicity doses (TD50) of 599.8, >1000, >1000 mg/kg, respectively, resulting in a protective index (PI) of 27.5, >42.9, >48.8, respectively. This is a much better protective index than that of the marked anti-epileptic drug valproate (PI = 1.6). To further investigate the effects of the anticonvulsant activity in several different models, compounds 1g, 1l, and 1n were tested having evoked convulsions with chemical substances, including pentylenetetrazloe, isoniazide, 3-mercaptopropionic acid, bicuculline, thiosemicarbazide, and strychnine.

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