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Diisopropyl sebacate is an organic compound that belongs to the ester class. It is characterized by its ability to act as a solvent and emollient, making it a versatile ingredient in various formulations.

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  • 7491-02-3 Structure
  • Basic information

    1. Product Name: Diisopropyl sebacate
    2. Synonyms: Decanedioicacid,bis(1-methylethyl)ester;decanedioicaciddiisopropylester;SCHERCEMOL DIISOPROPYL SEBACATE;SCHERCEMOL DIS;DIISOPROPYL SEBACATE;Di isopropyl Sebacate (DIPS);dipropan-2-yl decanedioate
    3. CAS NO:7491-02-3
    4. Molecular Formula: C16H30O4
    5. Molecular Weight: 286.41
    6. EINECS: 231-306-4
    7. Product Categories: N/A
    8. Mol File: 7491-02-3.mol
    9. Article Data: 2
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 308.2°Cat760mmHg
    3. Flash Point: 134.9°C
    4. Appearance: /
    5. Density: 0.953g/cm3
    6. Vapor Pressure: 0.00069mmHg at 25°C
    7. Refractive Index: 1.443
    8. Storage Temp.: Refrigerator
    9. Solubility: Chloroform (Slightly), Ethyl Acetate (Very Slightly)
    10. Water Solubility: 2mg/L at 20℃
    11. CAS DataBase Reference: Diisopropyl sebacate(CAS DataBase Reference)
    12. NIST Chemistry Reference: Diisopropyl sebacate(7491-02-3)
    13. EPA Substance Registry System: Diisopropyl sebacate(7491-02-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 7491-02-3(Hazardous Substances Data)

7491-02-3 Usage

Uses

Used in Cosmetic Industry:
Diisopropyl sebacate is used as an emollient in cosmetic formulations for its ability to soften and smooth the skin, providing a pleasant texture and feel.
Used in Fragrance Industry:
Diisopropyl sebacate is used as a solvent, particularly for fragrances, due to its ability to dissolve and stabilize aromatic compounds, ensuring their even distribution and long-lasting scent.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 7491-02-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7491-02:
(6*7)+(5*4)+(4*9)+(3*1)+(2*0)+(1*2)=103
103 % 10 = 3
So 7491-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H30O4/c1-13(2)19-15(17)11-9-7-5-6-8-10-12-16(18)20-14(3)4/h13-14H,5-12H2,1-4H3

7491-02-3SDS

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 Diisopropyl sebacate

1.2 Other means of identification

Product number -
Other names SCHERCEMOL DIS

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:7491-02-3 SDS

7491-02-3Downstream Products

7491-02-3Relevant articles and documents

Ozonolytic transformations of 10-undecenoic acid in various solvents through the action of hydroxylamine and semicarbazide hydrochlorides

Ishmuratov,Legostaeva,Nasibullina,Garifullina,Botsman,Tolstikov

, p. 594 - 597 (2015/02/02)

Ozonolytic transformations of 10-undecenoic acid, which is available from castor oil, were studied. Syntheses of several α,ω-bifunctional sebacic acid derivatives were developed.

Cosmetic composition

-

, (2008/06/13)

A composition suitable for topical application to mammalian skin or hair for inducing, maintaining or increasing hair growth comprises: (i) a first chemical inhibitor chosen from proteoglycanase inhibitors, glycosaminoglycanase inhibitors, glycosaminoglycan chain cellular uptake inhibitors or mixtures thereof; and (ii) a cosmetically acceptable vehicle for the chemical inhibitor; provided that when the first chemical inhibitor is a weak inhibitor, such that a 1 mM aqueous solution of the inhibitor reduces proteoglycanase activity, glycosaminoglycanase activity or cellular uptake of glycosaminoglycan chains, by from 5 to 50%, in accordance with at least one of the assay tests as herein described, then there is also present in the composition a second chemical inhibitor and/or an activity enhancer. When minoxidil is the sole chemical inhibitor, then the activity enhancer is a penetration enhancer chosen from a limited number of materials, including certain esters and cationic polymers. The total amount of chemical inhibitor present in the composition is sufficient to increase hair growth in the rat, when said composition is applied topically thereto, by at least 10% more than that obtainable using a control composition from which the said inhibitors have been omitted.

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