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38835-17-5

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38835-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38835-17-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,3 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 38835-17:
(7*3)+(6*8)+(5*8)+(4*3)+(3*5)+(2*1)+(1*7)=145
145 % 10 = 5
So 38835-17-5 is a valid CAS Registry Number.

38835-17-5SDS

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 2,3-dihydroxypropyl 2-(6-methoxynaphthalen-2-yl)propanoate

1.2 Other means of identification

Product number -
Other names (D,L)-1-naproxenoylglycerol

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:38835-17-5 SDS

38835-17-5Downstream Products

38835-17-5Relevant articles and documents

Diacyl glyceryl ester prodrugs for slow release in the skin: Synthesis and in vitro degradation and absorption studies for naproxen derivatives

Thorsteinsson,Masson, Mar,Loftsson,Haraldsson,Stefansson

, p. 831 - 836 (2007/10/03)

Diacyl glyceryl ester derivatives of naproxen were synthesized and tested for transdermal and dermal administration. Diacyl derivatives of aliphatic acids of various chain length were compared. The pharmaceutical properties of these compounds, such as lipophilicity, hydrolysis in a buffer solution at various pH values and degradation in human serum and hairless mouse skin homogenate, were investigated. All the diacyl derivatives were relatively stable in a neutral buffer solution, but were rapidly degraded to release naproxen in human serum and hairless mouse skin homogenate. The diacyl compounds could not penetrate hairless mouse skin in vitro. However, significant absorption into the skin could be measured, and this increased with increasing lipophilicity. A more than 100-fold difference in absorption was observed. The prodrugs were slowly hydrolyzed to naproxen inside the skin. The release of naproxen to the receptor compartment of diffusion cells showed that this type of prodrug could be used for controlled drug delivery.

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