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sec-hexyl laurate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 55194-05-3 Structure
  • Basic information

    1. Product Name: sec-hexyl laurate
    2. Synonyms: sec-hexyl laurate;Lauric acid 1-methylpentyl ester;Dodecanoic acid, 1-methylpentyl ester;Einecs 259-520-3
    3. CAS NO:55194-05-3
    4. Molecular Formula: C18H36O2
    5. Molecular Weight: 284.47724
    6. EINECS: 259-520-3
    7. Product Categories: N/A
    8. Mol File: 55194-05-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 326.5°C at 760 mmHg
    3. Flash Point: 153.2°C
    4. Appearance: /
    5. Density: 0.863g/cm3
    6. Vapor Pressure: 0.000215mmHg at 25°C
    7. Refractive Index: 1.441
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: sec-hexyl laurate(CAS DataBase Reference)
    11. NIST Chemistry Reference: sec-hexyl laurate(55194-05-3)
    12. EPA Substance Registry System: sec-hexyl laurate(55194-05-3)
  • 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: 55194-05-3(Hazardous Substances Data)

55194-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55194-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,9 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55194-05:
(7*5)+(6*5)+(5*1)+(4*9)+(3*4)+(2*0)+(1*5)=123
123 % 10 = 3
So 55194-05-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H36O2/c1-4-6-8-9-10-11-12-13-14-16-18(19)20-17(3)15-7-5-2/h17H,4-16H2,1-3H3

55194-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name hexan-2-yl dodecanoate

1.2 Other means of identification

Product number -
Other names Laurinsaeure-2-hexylester

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:55194-05-3 SDS

55194-05-3Downstream Products

55194-05-3Relevant articles and documents

Enzyme reactions in apolar solvents. The resolution of branched and unbranched 2-alkanols by porcine pancreatic lipase

Morgani, Brian,Oehlschlager, Allan C.,Stokes, Thomas M.

, p. 1611 - 1620 (2007/10/02)

Straight-chain and branched 2-alkanols were subjected to enzyme catalyzed transesterification in organic solvent using porcine pancreatic lipase, high enantioselectivity being generally observed. The method was applied to the synthesis of (R)-(-)-9-hydroxy-(E)-decenoic acid, a component of the queen bee mandibular gland pheromone.

Fat Hydrolysis and Esterification by a Lipase from Humicola lanuginosa

Omar, Ibrahim Che,Nishio, Naomichi,Nagai, Shiro

, p. 2153 - 2160 (2007/10/02)

The hydrolysis and esterification by a thermostable lipase from Humicola lanuginosa No. 3 were investigated.Both reactions occurred readily at temperatures between 45-50 deg C.Esterification by the enzyme with glycerol was observed to be specific towards fatty acids with carbon numbers of C12-C18.Lauric acid esters with different alcohols such as primary alcohols, terpene alcohols, etc., were also synthesized readily.Esterification by the enzyme was adversely affected by the water content (optimum, ca. 7percent), however, the hydrolysis rate increased rapidly with increasing water content (optimum, ca. 60percent).The enzyme showed increased activity in organic solvent-aqueous reaction systems.Nevertheless, hydrolysis in complete organic phase reactions was found not to be feasible.Hydrolysis at a higher temperature (50 or 55 deg C) in a solvent free phase was almost the same as that in organic solvent-aqueous phase reactions.The components of glycerides varied considerably during hydrolysis, whereby esterification resulted in a higher quantity of mono- and diglycerides (about 40percent), compared to in the case of hydrolysis, for which the value was about 10-20percent.

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