1. Home
  2. 1-Docosanol, hydrogen sulfate, sodium salt

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1-Docosanol, hydrogen sulfate, sodium salt

CCCCCCCCCCCCCCCCCCCCCCOS(=O)(=O)[O-].[Na+] Request for Quotation
Chemical Name: 1-Docosanol, hydrogen sulfate, sodium salt
CAS Number: 13177-50-9
Product Number: AG000ZPM(AGN-PC-0PJJCZ)
Synonyms:
MDL No:
Molecular Formula: C22H45NaO4S
Molecular Weight: 428.6451

Identification/Properties

Properties
MP:
198-201 °C
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
428.648g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
22
Exact Mass:
428.294g/mol
Monoisotopic Mass:
428.294g/mol
Topological Polar Surface Area:
74.8A^2
Heavy Atom Count:
28
Formal Charge:
0
Complexity:
383
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Sodium dodecyl sulfate, also known as SDS or sodium lauryl sulfate, is a widely used anionic surfactant in chemical synthesis. Its application in organic chemistry is primarily seen in various reactions where emulsification, solubilization, and micellar catalysis are required. SDS is frequently used in micellar catalysis to enhance reaction rates by providing a stable micellar environment that can increase the solubility of hydrophobic reactants. This surfactant can solubilize nonpolar compounds in aqueous solutions by forming micelles, which are structures that encapsulate hydrophobic molecules, allowing them to stay dispersed in the solution.In addition to its role in catalysis, SDS is also utilized in the purification and separation of biomolecules and proteins. It is commonly employed in techniques such as gel electrophoresis to denature proteins and facilitate their migration through the gel matrix.Furthermore, SDS is often utilized in the synthesis and modification of nanoparticles, where its surfactant properties help in stabilizing the nanoparticle suspension and controlling their size and shape during synthesis.Overall, Sodium dodecyl sulfate plays a crucial role in chemical synthesis by enabling the solubilization, stabilization, and catalysis of various compounds and reactions in aqueous environments.