122-19-0,MFCD00149986
Catalog No.:AA0035JJ

122-19-0 | Stearyldimethylbenzylammonium chloride

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98% +(isomers mixture)(contains<5%H2O)
in stock  
$10.00   $7.00
- +
25g
95%
in stock  
$40.00   $28.00
- +
100g
95%
in stock  
$154.00 $108.00
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0035JJ
Chemical Name:
Stearyldimethylbenzylammonium chloride
CAS Number:
122-19-0
Molecular Formula:
C27H50ClN
Molecular Weight:
424.1456
MDL Number:
MFCD00149986
SMILES:
CCCCCCCCCCCCCCCCCC[N+](Cc1ccccc1)(C)C.[Cl-]
NSC Number:
20199
UN Number:
2811
Properties
Properties
 
Form:
Solid  
MP:
54-56°C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
316  
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
29  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
19  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  

Downstream Synthesis Route

[1]Tanakaetal.[YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1943,vol.63,p.589][Chem.Abstr.,1951,p.5100]CurrentPatentAssignee:I.G.FARBENINDUSTRIEAG(historic)-CH184535,1934,A

[2]Chernyavskaya,M.A.;Stefanovich,V.V.;Sergeeva,I.A.;Belova,A.S.[PharmaceuticalChemistryJournal,1984,vol.18,#11,p.784-787][Khimiko-FarmatsevticheskiiZhurnal,1984,vol.18,#11,p.1344-1348]

[3]Campanac;Pineau;Payard;Baziard-Mouysset;Roques[AntimicrobialAgentsandChemotherapy,2002,vol.46,#5,p.1469-1474]

[4]CurrentPatentAssignee:JIANGNANUNIVERSITY-CN106431995,2017,ALocationinpatent:Paragraph0042;0043;0048;0049

[1]Chernyavskaya,M.A.;Stefanovich,V.V.;Sergeeva,I.A.;Belova,A.S.[PharmaceuticalChemistryJournal,1984,vol.18,#11,p.784-787][Khimiko-FarmatsevticheskiiZhurnal,1984,vol.18,#11,p.1344-1348]

[1]PharmaceuticalChemistryJournal,1984,vol.18,p.784-787    Khimiko-FarmatsevticheskiiZhurnal,1984,vol.18,p.1344-1348

C34H64O11 
  122-19-0   
C27H50N(1+)*C34H63O11(1-) 

[1]CurrentPatentAssignee:BIOSILRESINST-US6372934,2002,B1Locationinpatent:Pagecolumn7

Literature

Title: Adsorption of zearalenone by organomodified natural zeolitic tuff.

Journal: Journal of colloid and interface science 20070701

Title: Adsorption of mycotoxins by organozeolites.

Journal: Colloids and surfaces. B, Biointerfaces 20051125

Title: A K Palmer, et al. Absence of embryotoxic effects in rats with three quaternary ammonium compounds (cationic surfactants). Toxicology. Mar-Apr 1983;26(3-4):313-5.

Quotation Request
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Additional Info:
SDS
Tags:122-19-0 Molecular Formula|122-19-0 MDL|122-19-0 SMILES|122-19-0 Stearyldimethylbenzylammonium chloride
Catalog No.: AA0035JJ
122-19-0,MFCD00149986
122-19-0 | Stearyldimethylbenzylammonium chloride
Pack Size: 5g
Purity: 98% +(isomers mixture)(contains<5%H2O)
in stock
$10.00 $7.00
Pack Size: 25g
Purity: 95%
in stock
$40.00 $28.00
Pack Size: 100g
Purity: 95%
in stock
$154.00 $108.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0035JJ
Chemical Name: Stearyldimethylbenzylammonium chloride
CAS Number: 122-19-0
Molecular Formula: C27H50ClN
Molecular Weight: 424.1456
MDL Number: MFCD00149986
SMILES: CCCCCCCCCCCCCCCCCC[N+](Cc1ccccc1)(C)C.[Cl-]
NSC Number: 20199
UN Number: 2811
Properties
Form: Solid  
MP: 54-56°C  
Storage: Keep in dry area;Room Temperature;  
Complexity: 316  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 29  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 19  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
Downstream Synthesis Route
124-28-7    100-44-7    122-19-0 

[1]Tanakaetal.[YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1943,vol.63,p.589][Chem.Abstr.,1951,p.5100]CurrentPatentAssignee:I.G.FARBENINDUSTRIEAG(historic)-CH184535,1934,A

[2]Chernyavskaya,M.A.;Stefanovich,V.V.;Sergeeva,I.A.;Belova,A.S.[PharmaceuticalChemistryJournal,1984,vol.18,#11,p.784-787][Khimiko-FarmatsevticheskiiZhurnal,1984,vol.18,#11,p.1344-1348]

[3]Campanac;Pineau;Payard;Baziard-Mouysset;Roques[AntimicrobialAgentsandChemotherapy,2002,vol.46,#5,p.1469-1474]

[4]CurrentPatentAssignee:JIANGNANUNIVERSITY-CN106431995,2017,ALocationinpatent:Paragraph0042;0043;0048;0049

112-92-5    122-19-0 

[1]Chernyavskaya,M.A.;Stefanovich,V.V.;Sergeeva,I.A.;Belova,A.S.[PharmaceuticalChemistryJournal,1984,vol.18,#11,p.784-787][Khimiko-FarmatsevticheskiiZhurnal,1984,vol.18,#11,p.1344-1348]

3386-33-2    122-19-0 

[1]PharmaceuticalChemistryJournal,1984,vol.18,p.784-787    Khimiko-FarmatsevticheskiiZhurnal,1984,vol.18,p.1344-1348

C34H64O11 
  122-19-0   
C27H50N(1+)*C34H63O11(1-) 

[1]CurrentPatentAssignee:BIOSILRESINST-US6372934,2002,B1Locationinpatent:Pagecolumn7

Literature fold

Title: Adsorption of zearalenone by organomodified natural zeolitic tuff.

Journal: Journal of colloid and interface science20070701

Title: Adsorption of mycotoxins by organozeolites.

Journal: Colloids and surfaces. B, Biointerfaces20051125

Title: A K Palmer, et al. Absence of embryotoxic effects in rats with three quaternary ammonium compounds (cationic surfactants). Toxicology. Mar-Apr 1983;26(3-4):313-5.

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