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About This Item
Linear Formula:
NH2(CH2)3COOCH3 · HCl
CAS Number:
Molecular Weight:
153.61
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3558996
Quality Level
assay
≥99.0% (AT)
form
crystals
reaction suitability
reaction type: solution phase peptide synthesis
color
colorless
mp
120-125 °C (lit.)
application(s)
peptide synthesis
SMILES string
Cl.COC(=O)CCCN
InChI
1S/C5H11NO2.ClH/c1-8-5(7)3-2-4-6;/h2-4,6H2,1H3;1H
InChI key
WPGPRLVPWACBHW-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
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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I N Tiurenkov et al.
Farmakologiia i toksikologiia, 49(6), 31-34 (1986-11-01)
In pentobarbital-anesthetized cats GABA methylester (MEG) and beta-phenyl-GABA methylester (MEF) administered intravenously in doses of 1/100, 1/30, 1/10 of LD50 and injected intracerebroventricularly in doses of 0.1 and 0.5 mg produce hypotension, These effects are significantly suppressed by picrotoxin. These
M Bianchi et al.
Biochemical pharmacology, 32(6), 1093-1096 (1983-03-15)
4-Aminobutyric methyl ester hydrochloride (GME) is able to cross the blood-brain barrier after intracardiac administration to the rat. GME has an LD50 of 1300 mg/kg in mice and 950 mg/kg in rats, exhibits an antiaggressive effect and is able to
Michael R Emmett et al.
The Journal of organic chemistry, 77(15), 6634-6637 (2012-07-11)
Cyclopropane hemimalonates, when treated with sodium azide, undergo a tandem ring-opening decarboxylation to produce γ-azidobutyric acids in good yields. These adducts were hydrogenated to form γ-aminobutyric acid (GABA) methyl esters.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 07245-100G | 04061832593159 |
| 07245-25G | 04061832593166 |
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