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14450-05-6

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14450-05-6 Usage

Description

2,2-bis[[(1-oxononyl)oxy]methyl]propane-1,3-diyl dinonan-1-oate is a complex ester compound characterized by a propane-1,3-diyl core with two 1-oxononyl groups esterified to nonan-1-oate groups. It is part of the ester class of compounds, which are formed through the reaction between an alcohol and an acid. This chemical is recognized for its emollient and surfactant properties, making it a valuable ingredient in a variety of products.

Uses

Used in Cosmetics and Personal Care Products:
2,2-bis[[(1-oxononyl)oxy]methyl]propane-1,3-diyl dinonan-1-oate is used as an emollient and surfactant for its ability to soften and smooth the skin, as well as to reduce surface tension, facilitating the even distribution of products on the skin.
Used in Household Cleaners:
In the household cleaning industry, 2,2-bis[[(1-oxononyl)oxy]methyl]propane-1,3-diyl dinonan-1-oate is used as a surfactant to help break down and remove dirt and grease, making it easier to clean various surfaces.
Used as a Stabilizer and Solubilizer:
2,2-bis[[(1-oxononyl)oxy]methyl]propane-1,3-diyl dinonan-1-oate is utilized as a stabilizer and solubilizer in formulations to improve the solubility of other ingredients and to maintain the stability of the final product.
Safety Precautions:
It is crucial to handle 2,2-bis[[(1-oxononyl)oxy]methyl]propane-1,3-diyl dinonan-1-oate with care due to its potential to cause skin and eye irritation. It should not be ingested or inhaled to prevent any adverse health effects.

Check Digit Verification of cas no

The CAS Registry Mumber 14450-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,5 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14450-05:
(7*1)+(6*4)+(5*4)+(4*5)+(3*0)+(2*0)+(1*5)=76
76 % 10 = 6
So 14450-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C41H76O8/c1-5-9-13-17-21-25-29-37(42)46-33-41(34-47-38(43)30-26-22-18-14-10-6-2,35-48-39(44)31-27-23-19-15-11-7-3)36-49-40(45)32-28-24-20-16-12-8-4/h5-36H2,1-4H3

14450-05-6SDS

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 [3-nonanoyloxy-2,2-bis(nonanoyloxymethyl)propyl] nonanoate

1.2 Other means of identification

Product number -
Other names tetra-O-nonanoyl-pentaerythritol

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:14450-05-6 SDS

14450-05-6Downstream Products

14450-05-6Relevant articles and documents

An efficient catalyst COK-15b for the catalytic synthesis of lubricating ester oils

Wang, Yanan,Ma, Rui,Jiang, Cheng,Lou, Wenjing,Wang, Xiaobo

, p. 28 - 32 (2019/01/24)

The new material MOF of (CTA)1/3[Cu46(C9H3O6)24(OH)12] (PW12O40)3·xH2O (COK-15b) was synthesized via a dual-templating approach and exhibited high activity and selectivity for the esterification of pentaerythrotol with fatty acids at stoichiometric ratio to the corresponding pentaerythrotol tetra-esters with up to 98% yields under solvent-free conditions. The COK-15b was characterized by TEM, SEM, TG, BET, TPD and Py-IR. Moreover, the stability of COK-15b was investigated, and it can be reused for 5 running cycles without significant deactivation.

MIXTURES OF PELARGONIC ACID ESTERS.

-

Page/Page column 17; 18, (2017/03/28)

Mixture of at least two esters selected from neopentylglycol dipelargonate, glycerol tripelargonate, pentaerythritol tetrapelargonate, and use thereof in cosmetic compositions for the care, the make-up, the protection from the sun and for the cleansing of the skin and skin appendages.

Polymer containing a polyisobutylene-derived backbone

-

, (2008/06/13)

Polymers, such as polysiobutylene or ethylene-propylene copolymers, are functionalized by reaction with an activated imine to yield novel polymers.

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