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100186-17-2

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100186-17-2 Usage

Type

Chemical compound

Derivative of

Resorcinol

Industries

Pharmaceutical, cosmetic, plastics, and rubber

Uses

a. Phenolic antioxidant
b. Skin-lightening agent
c. Stabilizer
d. UV absorber

Potential properties

a. Anti-inflammatory
b. Anti-cancer

Appearance

White crystalline

Solubility

Soluble in alcohol, acetone, and ether

Check Digit Verification of cas no

The CAS Registry Mumber 100186-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,8 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 100186-17:
(8*1)+(7*0)+(6*0)+(5*1)+(4*8)+(3*6)+(2*1)+(1*7)=72
72 % 10 = 2
So 100186-17-2 is a valid CAS Registry Number.

100186-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-Methyl-2-hexanyl)-1,2-benzenediol

1.2 Other means of identification

Product number -
Other names -

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:100186-17-2 SDS

100186-17-2Relevant articles and documents

Effect of Crown Ether Lipophilicity on the Facilitated Transport of Guanidinium Thiocyanate through an Immobilized Liquid Membrane

Stolwijk, Theodorus B.,Sudhoelter, Ernst J. R.,Reinhoudt, David N.

, p. 6321 - 6329 (2007/10/02)

The flux of guanidinium thiocyanate through a supported liquid membrane has been measured for substituted benzo crown ethers and dibenzo crown ethers.This flux depends on the water solubility of the carrier.The more lipophilic crown ethers (7-14 and 16) show a higher flux and form more stable supported liquid membranes.The effect of the lipophilic substituents on the partition coefficient of the benzo crown ethers has been calculated and verified by partition experiments.The observed fluxes have been interpreted by a developed general model for the transport of salts through supported liquid membranes containing crown ethers.This thermodynamic model takes into account the interface equilibria, viz. the partition of crown ether and salt, as well as complexation equilibria in the membrane and aqueous phase.The model has been applied for the calculation of the complexation constants in the membrane phase.The lipophilic benzo crown ethers with 27 ring atoms show lower complexation constants than the corresponding benzo crown ether with 30 ring atoms.The complexation constants of the dibenzo crown ethers and guanidinium thiocyanate are smaller than those of the corresponding complexes of the substituted benzo crown ethers.During the diffusion process of the complex through the membrane phase complexation and decomplexation take place continuously as was concluded from the small value of the inverse Damkoehler number.

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