06720
2-Aminoethyl hydrogen sulfate
≥98.0% (T)
Synonym(s):
Sulfuric acid mono 2-aminoethylester
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About This Item
Linear Formula:
NH2CH2CH2OSO3H
CAS Number:
Molecular Weight:
141.15
Beilstein:
1704079
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
≥98.0% (T)
mp
277 °C (dec.) (lit.)
functional group
amine
SMILES string
NCCOS(O)(=O)=O
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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Related Categories
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
R Horton et al.
General pharmacology, 19(3), 403-405 (1988-01-01)
1. Oral administration of the GABA transaminase inhibitor ethanolamine-O-sulphate (EOS, 5 mg/ml in drinking water) to rats for 14 days suppressed food intake by 24%, but reduced weight gain by over 35%. 2. Thus, feed efficiency (g gain/MJ eaten) was
D V Coscina et al.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity, 16(6), 425-433 (1992-06-01)
To explore recent suggestions that genetically obese Zucker rats show less anorexia when brain gamma-aminobutyric acid (GABA) is elevated, obese vs. lean littermates received 100, 50 and 0 micrograms of the GABA-transaminase inhibitor, ethanolamine-O-sulfate (EOS), intra-cisternally in a longitudinal design
J P Loeffler et al.
Neuroendocrinology, 43(4), 504-510 (1986-01-01)
The inhibitory action of gamma-aminobutyric acid (GABA) on prolactin (PRL) messenger ribonucleic acid (mRNA) levels was studied in vitro in rat anterior pituitary cells in culture and in intact rats in vivo. PRL mRNA levels were determined by hybridization of
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
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