Welcome to LookChem.com Sign In|Join Free
  • or
3-Hydroxypropyl hexanoate, also known as 3-hydroxypropyl caprylate, is a chemical compound with the molecular formula C11H20O4. It is an ester derived from the reaction of 3-hydroxypropionic acid (lactic acid) and hexanoic acid (caprylic acid). This organic compound is characterized by its ability to form a clear, colorless liquid with a mild, pleasant odor. It is widely used in the pharmaceutical and cosmetic industries as a skin conditioning agent, emollient, and solvent. Due to its compatibility with the skin's natural moisturizing factors, 3-hydroxypropyl hexanoate helps to maintain skin hydration and improve its overall appearance. Additionally, it is known for its ability to enhance the stability and solubility of other ingredients in formulations, making it a valuable component in various personal care products.

6963-48-0

Post Buying Request

6963-48-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6963-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6963-48-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6963-48:
(6*6)+(5*9)+(4*6)+(3*3)+(2*4)+(1*8)=130
130 % 10 = 0
So 6963-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O3/c1-2-3-4-6-9(11)12-8-5-7-10/h10H,2-8H2,1H3

6963-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxypropyl hexanoate

1.2 Other means of identification

Product number -
Other names Hexanoic acid,3-hydroxypropyl ester

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:6963-48-0 SDS

6963-48-0Downstream Products

6963-48-0Relevant academic research and scientific papers

Facile oxidative hydrolysis of acetals to esters using hypervalent iodine(III)/LiBr combination in water

Panchan, Waraporn,Chiampanichayakul, Supanimit,Snyder, Deanna L.,Yodbuntung, Siriporn,Pohmakotr, Manat,Reutrakul, Vichai,Jaipetch, Thaworn,Kuhakarn, Chutima

experimental part, p. 2732 - 2735 (2010/05/17)

The combination of (diacetoxy)iodobenzene (PhI(OAc)2, DIB) and lithium bromide (LiBr) efficiently oxidized cyclic and acyclic acetals to the corresponding hydroxyalkyl carboxylic esters and simple esters in good to excellent yields. The merits of this reaction are that it employs commercially available and non-explosive hypervalent iodine(III) reagent, water as the solvent, a short reaction time, and mild reaction conditions.

Oxone: A convenient reagent for the oxidation of acetals

Curini, Massimo,Epifano, Francesco,Marcotullio, Maria Carla,Rosati, Ornelio

, p. 777 - 779 (2007/10/03)

Symmetrical cyclic and acyclic acetals by oxidation with Oxone gave the corresponding esters in good yield. Treatment of tetrahydropyranyl derivatives of alcohols with the same reagent resulted in oxidative regeneration of the alcohols.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6963-48-0