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
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
213-135-7
MDL number:
Beilstein/REAXYS Number:
1704079
Assay:
≥98.0% (T)
InChI key
WSYUEVRAMDSJKL-UHFFFAOYSA-N
InChI
1S/C2H7NO4S/c3-1-2-7-8(4,5)6/h1-3H2,(H,4,5,6)
assay
≥98.0% (T)
mp
277 °C (dec.) (lit.)
functional group
amine
Quality Level
Related Categories
signalword
Warning
hcodes
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
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
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)
M Qume et al.
Biochemical pharmacology, 52(9), 1355-1363 (1996-11-08)
The inhibitory neurotransmitter gamma-aminobutyric acid (GABA) is not solely located in the CNS, it and the enzymes responsible for its synthesis (glutamic acid decarboxylase, GAD, EC 4.1.1.15) and catabolism (GABA-transaminase, GABA-T, EC 2.6.1.19) are also present in non-neuronal organs. Following
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
GABA-mimetic compounds block haloperidol-induced hyperprolactinemia in rats.
L Debeljuk et al.
Advances in biochemical psychopharmacology, 42, 139-144 (1986-01-01)
Célia M C Faustino et al.
The journal of physical chemistry. B, 113(4), 977-982 (2009-01-23)
New anionic urea-based surfactants derived from alpha,omega-amino acids and in particular from beta-alanine were synthesized and their solution properties characterized by electrical conductivity, equilibrium surface tension, and steady-state fluorescence spectroscopy techniques. Double-chain surfactants and the single-chain surfactant containing a sulfate
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