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28522-49-8

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28522-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28522-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,2 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28522-49:
(7*2)+(6*8)+(5*5)+(4*2)+(3*2)+(2*4)+(1*9)=118
118 % 10 = 8
So 28522-49-8 is a valid CAS Registry Number.
InChI:InChI=1/C43H88O3/c1-4-7-10-13-16-19-22-23-24-25-27-30-33-36-39-45-42-43(46-40-37-34-31-28-21-18-15-12-9-6-3)41-44-38-35-32-29-26-20-17-14-11-8-5-2/h43H,4-42H2,1-3H3

28522-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,3-didodecoxypropoxy)hexadecane

1.2 Other means of identification

Product number -
Other names Hexadecane,1-(2,3-bis(dodecyloxy)propoxy)

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:28522-49-8 SDS

28522-49-8Upstream product

28522-49-8Downstream Products

28522-49-8Relevant articles and documents

Synthesis and metabolism of glycerol-3H triether, a nonabsorbable oil-phase marker for lipid absorption studies.

Morgan,Hofmann

, p. 223 - 230 (2007/10/12)

A saturated mixed-chain glycerol triether, 1-hexadecyl-2,3-didodecyl glycerol (1-hexadecoxy-2,3-didodecoxypropane), was synthesized with (3)H at positions 9 and 10 or (14)C at position 1 of the hexadecyl moiety. In acute feeding experiments in rats, less than 0.2% of the triether was absorbed, based on lymph and fecal recoveries. Radioactivity was present exclusively as triether in feces, indicating that it was not degraded by digestive or bacterial enzymes. Chronic feeding experiments in rats confirmed the nonabsorbability of the triether and further indicated that it was nontoxic, did not influence the absorption of dietary fat, and mixed intimately with the fat present in colonic contents and feces. The triether that was absorbed was deposited as triether in adipose tissue, liver, and spleen. When administered intraperitoneally to mice, the triether was stored in the tissues and was not metabolized. When the triether was partitioned between an oil phase of triolein or fatty acid and monoglyceride, and an aqueous micellar phase, the triether remained exclusively in the oil phase. The triether appears to be an ideal nonabsorbable oil-phase marker for use in lipid absorption studies.

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