Home Amines 926-39-6
926-39-6,MFCD00008179
Catalog No.:AA003GGI

926-39-6 | 2-Aminoethyl hydrogen sulfate

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5g
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10g
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$12.00   $8.00
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25g
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003GGI
Chemical Name:
2-Aminoethyl hydrogen sulfate
CAS Number:
926-39-6
Molecular Formula:
C2H7NO4S
Molecular Weight:
141.1463
MDL Number:
MFCD00008179
SMILES:
NCCOS(=O)(=O)O
Properties
Properties
 
Form:
Solid  
MP:
277 °C (dec.)(lit.)  
Refractive Index:
1.5130 (estimate)  
Storage:
Room Temperature;Light sensitive;Inert atmosphere;  

Computed Properties
 
Complexity:
133  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
3  
XLogP3:
-4.1  

Upstream Synthesis Route

[1]DRP/DRBPOrg.Chem.,

[2]DRP/DRBPOrg.Chem.,

[1]Patent:CN107739349,2018,A,.Locationinpatent:Paragraph0054

[2]AgriculturalandBiologicalChemistry,1991,vol.55,#10,p.2537-2546

[3]JournaloftheAmericanChemicalSociety,1947,vol.69,p.1540

[4]Patent:US2264759,1939,,

[5]ChemischeBerichte,1918,vol.51,p.1662

[6]JournaloftheAmericanChemicalSociety,1935,vol.57,p.2328

[7]JournaloftheAmericanChemicalSociety,1938,vol.60,p.2312

[8]JournalofOrganicChemistry,1965,vol.30,p.491-495

[9]HelveticaChimicaActa,1964,vol.47,p.2106-2112

[10]AgriculturalandBiologicalChemistry,1988,vol.52,#11,p.2911-2918

[11]HeterocyclicCommunications,2010,vol.16,#4-6,p.275-278

[12]JournalofHeterocyclicChemistry,2012,vol.49,#6,p.1370-1375

[13]MagneticResonanceinChemistry,2013,vol.51,#7,p.431-434

[14]DRP/DRBPOrg.Chem.,

[1]Patent:US4597911,1986,A,

[1]Patent:US4864045,1989,A,

[1]JournalofHeterocyclicChemistry,1972,vol.9,p.891-894

Downstream Synthesis Route

[1]Patent:DE744996,1940,    DRP/DRBPOrg.Chem.,

3140-73-6    926-39-6   
sulfuricacidmono-2-(4,6-dimethoxy-1,3,5triazin-2-ylamino)-ethylester;sodium-salt 

[1]JournaloftheAmericanChemicalSociety,1955,vol.77,p.5922,5926

[1]Patent:US2689867,1948,

[1]Patent:WO2008/63721,2008,A2.Locationinpatent:Page/Pagecolumn83-85

[2]JournaloftheAmericanChemicalSociety,1955,vol.77,p.5915,5917

[3]JournaloftheAmericanChemicalSociety,1955,vol.77,p.5915,5917

[4]MagneticResonanceinChemistry,2013,vol.51,p.431-434

[5]Patent:DE832152,1948,    DRP/DRBPOrg.Chem.,

[6]Patent:DE832152,1948,    DRP/DRBPOrg.Chem.,

Literature

Title: A modified rapid enzymatic microtiter plate assay for the quantification of intracellular γ-aminobutyric acid and succinate semialdehyde in bacterial cells.

Journal: Journal of microbiological methods 20110101

Title: New urea-based surfactants derived from alpha,omega-amino acids.

Journal: The journal of physical chemistry. B 20090129

Title: Identification of sulfation sites of metabolites and prediction of the compounds' biological effects.

Journal: Analytical and bioanalytical chemistry 20061001

Title: GABA-mediated effects of some taurine derivatives injected i.c.v. on rabbit rectal temperature and gross motor behavior.

Journal: Amino acids 20060501

Title: Interactions of taurine and structurally related analogues with the GABAergic system and taurine binding sites of rabbit brain.

Journal: British journal of pharmacology 20030301

Title: Participation of GABAergic mechanisms in the hypotensive and bradycardic effects of clonidine: experimental study in conscious normotensive and hypertensive rats.

Journal: Neuropharmacology 19871001

Title: Effects of inhibitors of GABA-transaminase on hole-board exploration and on temperature. Relation with effects on quasi-morphine abstinence behaviour induced by sodium dipropylacetate.

Journal: Biochemical pharmacology 19851101

Title: Blockade of methamphetamine-induced depression of tyrosine hydroxylase by GABA transaminase inhibitors.

Journal: European journal of pharmacology 19800829

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