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06720

Sigma-Aldrich

2-Aminoethyl hydrogen sulfate

≥98.0% (T)

Sinónimos:

Sulfuric acid mono 2-aminoethylester

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About This Item

Fórmula lineal:
NH2CH2CH2OSO3H
Número de CAS:
926-39-6
Peso molecular:
141.15
Beilstein/REAXYS Number:
1704079
EC Number:
213-135-7
MDL number:
MFCD00008179
UNSPSC Code:
12352100
PubChem Substance ID:
24845962
NACRES:
NA.22

assay

≥98.0% (T)

mp

277 °C (dec.) (lit.)

SMILES string

NCCOS(O)(=O)=O

InChI

1S/C2H7NO4S/c3-1-2-7-8(4,5)6/h1-3H2,(H,4,5,6)

InChI key

WSYUEVRAMDSJKL-UHFFFAOYSA-N

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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T Táira et al.
Psychopharmacology, 109(1-2), 191-197 (1992-01-01)
Long-term effects of chronic treatment with a GABA-T (GABA-transaminase) inhibitor, ethanolamine O-sulphate (EOS) (200 mg/kg/day for the postnatal days 3-21) on the binding parameters of GABAA receptors, hypothalamic monoamines and subsequent behavior were studied in Wistar rats. At the age
P Baud et al.
Brain research, 452(1-2), 203-211 (1988-06-14)
Locomotor activity in the rat was studied after infusion of GABAergic and enkephalinergic agonists into the nucleus basalis magnocellularis (NBM) of the forebrain. The experiments were designed to find out whether pharmacological blockade of cholinergic neurons in the NBM had
M Qume et al.
British journal of pharmacology, 122(3), 539-545 (1997-11-14)
1. The effects of 2, 8 and 21 day oral treatment with the specific gamma-aminobutyric acid transaminase (GABA-T) inhibitors gamma-vinyl GABA (GVG) and ethanolamine O-sulphate (EOS) on brain GABA levels, GABA-T activity, and basal and stimulated GABA release from rat
H Hodges et al.
Psychopharmacology, 89(2), 155-161 (1986-01-01)
Effects of chlordiazepoxide (CDP) and ethanolamine-O-sulphate (EOS) alone and in combination were tested on the acquisition and performance of continuous reinforcement - time out (CR-TO) and variable interval reinforcement - time out (VI-TO) operant discriminations in rats. CDP disrupted acquisition
R A John et al.
Biochemical pharmacology, 36(9), 1467-1473 (1987-05-01)
Two "suicide" inhibitors of GABA-aminotransferase which are known to raise the concentration of GABA in vivo and to have anti-convulsant properties, have been compared for the extent to which they produce micro-vacuoles in the brains of rats. The compounds gamma-vinyl-GABA
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