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63663-21-8

LAUROYL-L-GLUTAMIC-ALPHA,GAMMA-DIBUTYLAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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    Cas No: 63663-21-8

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  • 63663-21-8 Structure

  • Basic information

    1. Product Name: LAUROYL-L-GLUTAMIC-ALPHA,GAMMA-DIBUTYLAMIDE
    2. Synonyms: dibutyllauroylglutamide;N,N’-dibutyl-2-[(1-oxododecyl)amino]-,(S)-Pentanediamide;n’-dibutyl-2-[(1-oxododecyl)amino]-(s)-pentanediamid;Pentanediamide,N,N’-dibutyl-2-[(1-oxododecyl)amino]-,(2S)(9CI);Pentanediamide,N,N’-dibutyl-2-[(1-oxododecyl)amino]-,(S)-;LAUROYL-L-GLUTAMIC-ALPHA,GAMMA-DIBUTYLAMIDE;(S)-N,N'-dibutyl-2-[(1-oxododecyl)amino]glutaramide;Pentanediamide, N,N-dibutyl-2-(1-oxododecyl)amino-, (2S)-
    3. CAS NO:63663-21-8
    4. Molecular Formula: C25H48N2O4
    5. Molecular Weight: 440.66
    6. EINECS: 264-391-1
    7. Product Categories: N/A
    8. Mol File: 63663-21-8.mol

  • Chemical Properties

    1. Melting Point: 155～163℃
    2. Boiling Point: 678.5±50.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.957±0.06 g/cm3(Predicted)
    6. Vapor Pressure: 0Pa at 25℃
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 14.73±0.46(Predicted)
    11. Water Solubility: 12.57μg/L at 20℃
    12. CAS DataBase Reference: LAUROYL-L-GLUTAMIC-ALPHA,GAMMA-DIBUTYLAMIDE(CAS DataBase Reference)
    13. NIST Chemistry Reference: LAUROYL-L-GLUTAMIC-ALPHA,GAMMA-DIBUTYLAMIDE(63663-21-8)
    14. EPA Substance Registry System: LAUROYL-L-GLUTAMIC-ALPHA,GAMMA-DIBUTYLAMIDE(63663-21-8)

  • 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: 63663-21-8(Hazardous Substances Data)

63663-21-8 Usage

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 63663-21-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,6 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63663-21:
(7*6)+(6*3)+(5*6)+(4*6)+(3*3)+(2*2)+(1*1)=128
128 % 10 = 8
So 63663-21-8 is a valid CAS Registry Number.

63663-21-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-dibutyl-2-(dodecanoylamino)pentanediamide

1.2 Other means of identification

Product number -
Other names Pentanediamide,N,N'-dibutyl-2-[(1-oxododecyl)amino]

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:63663-21-8 SDS

63663-21-8Downstream Products

63663-21-8Relevant articles and documents

GELLING AGENT

-

Paragraph 0060; 0061; 0062; 0063, (2014/12/09)

Provided is a gelling agent containing N-acyl acidic amino acid dialkylamide having a DL form ratio (D form/L form (weight/weight)) of 5/95-20/80 or 80/20-95/5, and using the gelling agent, a gel composition, particularly a rod-like gel composition, superior in transparency and strength, and superior in compatibility and spreadability when applied to the skin, hair and the like is provided.

Process for production N-acyl amino acid amide

-

Example 2, (2008/06/13)

There is provided a process for producing an N-acyl amino acid amide, comprising a condensation reaction of an N-acyl amino acid with an amine and/or an ammonia, preferably a primary amine, a secondary amine and/or an ammonia under dehydration in the presence of a boron compound as the catalyst under coexistence of an alcohol as the auxiliary solvent, at a high yield for a short time. A medium for hylotropic dehydration such as hydrocarbon compounds may be used in the reaction.

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