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4595-26-0

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4595-26-0 Usage

Chemical Class

Organic compounds; specifically, benzene and substituted derivatives.

Primary Use

Skincare and cosmetic products.

Function

Antioxidant: Protects skin from damage caused by free radicals and UV radiation.
Skin-conditioning agent: Helps maintain skin hydration and overall health.

Source

Naturally occurring form of vitamin E, commonly derived from vegetable oils.

Additional Uses

Food additive: Prolongs the shelf life of products.

Versatility

Valuable chemical in skincare, cosmetic, and food industries.

Check Digit Verification of cas no

The CAS Registry Mumber 4595-26-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,9 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4595-26:
(6*4)+(5*5)+(4*9)+(3*5)+(2*2)+(1*6)=110
110 % 10 = 0
So 4595-26-0 is a valid CAS Registry Number.

4595-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hexadecylbenzene-1,4-diol

1.2 Other means of identification

Product number -
Other names Hexadecylhydroquinone

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:4595-26-0 SDS

4595-26-0Downstream Products

4595-26-0Relevant articles and documents

HYDROQUINONE LONG-CHAIN DERIVATIVE AND/OR PHENOXY LONG-CHAIN DERIVATIVE, AND PHARMACEUTICAL PREPARATION COMPRISING THE SAME

-

Page/Page column 20, (2008/06/13)

The present invention provides compounds represented by formula (1) shown below: (wherein R1, R2, R3, R4, and R5 are each individually selected from among a hydrogen atom, methyl group, acetyl group, hydroxyl group, and alkoxy group; and X represents an alkylene group or alkenylene group); and compounds represented by formula (2) shown below: (wherein R6, R7, R8, R9, and R10 are each individually selected from among a hydrogen atom, alkyl group, acetyl group, hydroxyl group, and alkoxy group; A represents an oxygen atom or NH, and m is 0 or 1; and Y represents an alkylene group or alkenylene group, and Z represents a hydrogen atom or hydroxyl group).The compounds of the present invention are useful for preventing or treating brain dysfunctions, motor dysfunctions, or urinary dysfunctions caused by the degeneration and/or loss of the central nervous system or peripheral nervous system cells.The present invention provides compounds represented by formula (1) shown below: (wherein R 1 , R 2 , R 3 , R 4 , and R 5 are each individually selected from among a hydrogen atom, methyl group, acetyl group, hydroxyl group, and alkoxy group; and X represents an alkylene group or alkenylene group); and compounds represented by formula (2) shown below: (wherein R 6 , R 7 , R 8 , R 9 , and R 10 are each individually selected from among a hydrogen atom, alkyl group, acetyl group, hydroxyl group, and alkoxy group; A represents an oxygen atom or NH, and m is 0 or 1; and Y represents an alkylene group or alkenylene group, and Z represents a hydrogen atom or hydroxyl group). The compounds of the present invention are useful for preventing or treating brain dysfunctions, motor dysfunctions, or urinary dysfunctions caused by the degeneration and/or loss of the central nervous system or peripheral nervous system cells.

Novel cytotoxic, alkylated hydroquinones from Lannea welwitschii

Groweiss, Amiram,Cardellina II, John H.,Pannell, Lewis K.,Uyakul, Duangchan,Kashman, Yoel,Boyd, Michael R.

, p. 116 - 121 (2007/10/03)

Two novel natural products, lanneaquinol (1) and 2'(R)- hydroxylanneaquinol (2), were isolated from the organic extract of the plant Lannea welwitschii (Hiern) Engl. Their structures were solved by spectroanalytical methods and confirmed by comparison to

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