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About This Item
Linear Formula:
NH2CH2CH2OSO3H
CAS Number:
Molecular Weight:
141.15
EC Number:
213-135-7
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
1704079
InChI
1S/C2H7NO4S/c3-1-2-7-8(4,5)6/h1-3H2,(H,4,5,6)
InChI key
WSYUEVRAMDSJKL-UHFFFAOYSA-N
assay
97%
mp
277 °C (dec.) (lit.)
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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A E Herbison et al.
Journal of neurochemistry, 55(5), 1617-1623 (1990-11-01)
The characteristics of gamma-aminobutyric acid (GABA) release as monitored by microdialysis have been investigated in the chloral hydrate anaesthetised rat. The high outflow of GABA following insertion of the microdialysis probe (membrane 2 mm in length, 0.5 mm in diameter)
GABA-mimetic compounds block haloperidol-induced hyperprolactinemia in rats.
L Debeljuk et al.
Advances in biochemical psychopharmacology, 42, 139-144 (1986-01-01)
H Golan et al.
Journal of neurophysiology, 71(1), 48-58 (1994-01-01)
1. The cytosolic concentration of a neurotransmitter is believed to be an important factor determining its release. The effects of ethanolamine-O-sulfate (EOS), a gamma-aminobutyric acid (GABA)-transaminase blocker, on GABAergic postsynaptic and presynaptic inhibitory neurotransmission were examined in the crayfish opener
D V Coscina et al.
Pharmacology, biochemistry, and behavior, 32(1), 275-281 (1989-01-01)
Intracisternal (IC) injection of the GABA-transaminase inhibitor, ethanolamine-O-sulfate (EOS), has been previously shown to induce dose-dependent anorexia in normal rats as well as to reverse overeating in several rodent models of acute and chronic hyperphagia. To determine if such anorexia
J Semba et al.
Neuropsychobiology, 21(3), 152-156 (1989-01-01)
We carried out the forced swimming test in mice to investigate the antidepressant potentials of GABA transaminase (GABA-T) inhibitors including aminooxyacetic acid, ethanolamine-O-sulfate, gamma-vinyl GABA (GVG) and valproic acid (VPA). In acute experiments only GVG reduced immobility. Following chronic oral
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