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Merck
모든 사진(1)

주요 문서

06720

Sigma-Aldrich

2-Aminoethyl hydrogen sulfate

≥98.0% (T)

동의어(들):

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 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

≥98.0% (T)

mp

277 °C (dec.) (lit.)

작용기

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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픽토그램

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신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

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
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
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
GABA-mimetic compounds block haloperidol-induced hyperprolactinemia in rats.
L Debeljuk et al.
Advances in biochemical psychopharmacology, 42, 139-144 (1986-01-01)

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