Polystyrene Resin

Product Information

Molecular Formula
C24H27NO5
Molecular Weight
409.18892296
Description
Polystyrene Resin is a versatile polymer widely utilized in biochemical applications due to its robust and adaptable properties. Known for its stability and resistance to chemical reactions, it serves as an essential component in various laboratory processes, including chromatography and solid-phase synthesis. The resin's structure allows for easy functionalization, making it a preferred choice for immobilizing biomolecules and facilitating complex biochemical reactions. Its compatibility with diverse solvents and reagents enhances its utility in research and industrial settings, providing a reliable medium for innovative biochemical developments.
Synonyms
Fmoc-Glu(OtBu)-H; tert-butyl (4S)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxopentanoate; (4S)-4-[[9H-fluoren-9-ylmethoxy(oxo)methyl]amino]-5-oxopentanoic acid tert-butyl ester; Fmoc-Glu(OtBu)-Wang resin; Fmoc-L-Glu(tBu)-Wang Resin (80-160 ?m, 1% DVB); Fmoc-L-Glu(tBu)-Wang Resin (200-400 mesh, 1% DVB); Fmoc-L-Glu(tBu)-Wang TentaGel S (90 ?m, 0.2-0.25 mmol/g); Fmoc-Glu(OtBu)-Wang resin, extent of labeling: 0.4-1.0 mmol/g loading; Fmoc-L-Glu(tBu)-4-methoxybenzhydryl resin (100-200 mesh, > 0.4 mmol/g); Fmoc-L-Glu(tBu)-4-methylbenzhydryl resin (100-200 mesh, > 0.3 mmol/g); Fmoc-L-Glu(tBu)-RinkAmide MBHA Resin (100-200 mesh, > 0.3 mmol/g); (S)-2-[(9H-Fluorene-9-ylmethoxycarbonyl)amino]-5-oxo-5-tert-butoxypentanal; 7-HYDROXY-5-METHYL-[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE-2-CARBOXYLICACID
IUPAC Name
tert-butyl (4S)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxopentanoate
Canonical SMILES
CC(C)(C)OC(=O)CCC(C=O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
InChI
InChI=1S/C24H27NO5/c1-24(2,3)30-22(27)13-12-16(14-26)25-23(28)29-15-21-19-10-6-4-8-17(19)18-9-5-7-11-20(18)21/h4-11,14,16,21H,12-13,15H2,1-3H3,(H,25,28)/t16-/m0/s1
InChI Key
BCIPGSZQUDLGSY-INIZCTEOSA-N
Boiling Point
654°C at 760 mmHg
Purity
20-60 mesh,1% DVB

Safety Information

Hazards
H302-H315-H319-H335
Precautionary Statement
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
GHS Pictogram
GHS07
Signal Word
Warning

Computed Properties

XLogP3
3.8
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
5
Rotatable Bond Count
10
Exact Mass
409.18892296
Monoisotopic Mass
409.18892296
Topological Polar Surface Area
81.7
Heavy Atom Count
30
Formal Charge
0
Complexity
591
Isotope Atom Count
0
Defined Atom Stereocenter Count
1
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
WO-2022256066-A1 Selective penicillamine substitution enables development of a potent analgesic peptide that acts through a non-opioid based mechanism 2021-06-03
EP-4023295-A1 Vegf-regulating peptides 2020-12-29
WO-2022144401-A1 Vegf-regulating peptides 2020-12-29
WO-2021023646-A1 Melanocyte-regulating peptides 2019-08-02
TW-202120117-A Melanocyte-regulating peptides 2019-08-02
CN-114245800-A melanocyte regulatory peptide 2019-08-02
EP-4007563-A1 Melanocyte-regulating peptides 2019-08-02
JP-2022542512-A Melanocyte regulatory peptide 2019-08-02
CA-3143676-A1 Constrained peptides 2019-06-19
CN-114206916-A restricted peptide 2019-06-19

Literatures

PMID Publication Date Title Journal
12608756 2003-02-01 Speciation of antimony using chromosorb 102 resin as a retention medium Analytical sciences : the international journal of the Japan Society for Analytical Chemistry
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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