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1-O,3-O-Dipalmitoyl-2-O-stearoyl-L-glycerol, also known as 1,3-Dipalmitoyl-2-stearoyl glycerol, is a triacylglycerol that features palmitic acid at the sn-1 and sn-3 positions and stearic acid at the sn-2 position. This specific arrangement of fatty acids contributes to its unique properties and potential applications.

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  • 2177-97-1 Structure
  • Basic information

    1. Product Name: 1-O,3-O-Dipalmitoyl-2-O-stearoyl-L-glycerol
    2. Synonyms: 1,2,3-Propanetriyl=1,3-dipalmitate 2-stearate;1,3-Dipalmito-2-stearin;1,3-Dipalmitoyl-2-stearin;1-O,3-O-Dipalmitoyl-2-O-stearoyl-L-glycerol;2-O-Stearoyl-1-O,3-O-bispalmitoylglycerol;2-Stearo-1,3-dipalmitin
    3. CAS NO:2177-97-1
    4. Molecular Formula: C53H102O6
    5. Molecular Weight: 835.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2177-97-1.mol
  • Chemical Properties

    1. Melting Point: 59.5 °C
    2. Boiling Point: 777.9±27.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.913±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-O,3-O-Dipalmitoyl-2-O-stearoyl-L-glycerol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-O,3-O-Dipalmitoyl-2-O-stearoyl-L-glycerol(2177-97-1)
    11. EPA Substance Registry System: 1-O,3-O-Dipalmitoyl-2-O-stearoyl-L-glycerol(2177-97-1)
  • 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: 2177-97-1(Hazardous Substances Data)

2177-97-1 Usage

Uses

Used in Pharmaceutical Industry:
1-O,3-O-Dipalmitoyl-2-O-stearoyl-L-glycerol is used as a component in the formulation of lipid-based drug delivery systems for enhancing the solubility, stability, and bioavailability of lipophilic drugs. Its unique fatty acid composition provides advantages in terms of controlled release and targeted drug delivery.
Used in Nutritional Research:
In the field of nutritional science, 1-O,3-O-Dipalmitoyl-2-O-stearoyl-L-glycerol is utilized as a model compound to study the effects of dietary fat intake on energy metabolism and body weight regulation. The observation of its levels in rats with reduced food intake-induced energy depletion provides insights into the role of triacylglycerols in energy balance and metabolism.
Used in Cosmetics Industry:
1-O,3-O-Dipalmitoyl-2-O-stearoyl-L-glycerol is employed as an ingredient in the cosmetics industry, particularly in the formulation of creams and lotions. Its emollient properties help to moisturize and protect the skin, while its stability contributes to the shelf life of cosmetic products.
Used in Food Industry:
In the food industry, 1-O,3-O-Dipalmitoyl-2-O-stearoyl-L-glycerol is used as an additive to improve the texture, mouthfeel, and stability of various food products. Its unique fatty acid composition may also play a role in the development of reduced-calorie or healthier food options by influencing the digestibility and absorption of fats.

Check Digit Verification of cas no

The CAS Registry Mumber 2177-97-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,7 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2177-97:
(6*2)+(5*1)+(4*7)+(3*7)+(2*9)+(1*7)=91
91 % 10 = 1
So 2177-97-1 is a valid CAS Registry Number.

2177-97-1SDS

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 β'-1,3-dihexadecanoyl-2-octadecanoyl-glycerol

1.2 Other means of identification

Product number -
Other names -

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:2177-97-1 SDS

2177-97-1Downstream Products

2177-97-1Relevant articles and documents

Interesterification Kinetics of Triglycerides and Fatty Acids with Modified Lipase in n-Hexane

Basheer, Sobhi,Mogi, Ken-ichi,Nakajima, Mitsutoshi

, p. 511 - 518 (2007/10/02)

The kinetics of lipase-catalyzed interesterification of triglycerides and fatty acids in organic media was studied.First, the lipase Saiken 100, Rhizopus japonicus, was modified by surfactant to form an enzyme precipitate in aqueous solution, which was well dispersed in organic solvents.This modified lipase catalyzed the interesterification of tripalmitin and stearic acid.The enzyme has 1,3-positional specificity and does not distinguish between stearic and palmitic acids.The kinetic model developed to describe the interesterification reaction system is based on mass balance of two consecutive second-order reversible reactions.The reaction rate constant, k, was determined by solving the differential rate equations of the reaction system and by expressing the value of k as a function of concentrations of the substrates with time.The model gave satisfactory results.The best value of the specific reaction rate constant k* that fits all experimental data was 1.2*10-5 2/(mmol*mg biocatalyst*h)> under the reaction conditions in this study. Key words: Acidolysis, biocatalyst, fatty acids, interesterification kinetics, modified lipase, palmitic acid, reaction rate constant, stearic acid, triglycerides.

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