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About This Item
Linear Formula:
(CH3)2CHCH2CH(NH2)COOC2H5 · HCl
CAS Number:
Molecular Weight:
195.69
Beilstein/REAXYS Number:
3994312
EC Number:
MDL number:
UNSPSC Code:
12352200
eCl@ss:
32160406
PubChem Substance ID:
Recommended Products
assay
≥99.0% (AT)
form
solid
optical activity
[α]20/D +18.0±1°, c = 5% in ethanol
mp
134-136 °C
application(s)
peptide synthesis
storage temp.
2-8°C
SMILES string
Cl.CCOC(=O)[C@@H](N)CC(C)C
InChI
1S/C8H17NO2.ClH/c1-4-11-8(10)7(9)5-6(2)3;/h6-7H,4-5,9H2,1-3H3;1H/t7-;/m0./s1
InChI key
NOUDPBCEONUCOV-FJXQXJEOSA-N
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Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Jaroslav Mráz et al.
Archives of toxicology, 93(3), 603-613 (2019-01-23)
Ethylene oxide (EO), a genotoxic industrial chemical and sterilant, forms covalent adducts with DNA and also with nucleophilic amino acids in proteins. The adduct with N-terminal valine in globin [N-(2-hydroxyethyl)valine (HEV)] has been used in biomonitoring of cumulative exposures to
Peter J Baker et al.
Macromolecular bioscience, 14(11), 1619-1626 (2014-08-27)
We report the encapsulation of three different proteases in bioinspired silica. Silica particles were formed under mild reaction conditions using cationic amine-rich ethyleneamines as initiators, which resulted in aggregations of nanoscale spheres. Following encapsulation, the proteases were characterized for their
David Schachter et al.
American journal of physiology. Gastrointestinal and liver physiology, 306(11), G938-G946 (2014-04-05)
The leucine-to-glutamate (Leu→Glu) pathway, which metabolizes the carbon atoms of l-leucine to form l-glutamate, was studied by incubation of rat tissue segments with l-[U-(14)C]leucine and estimation of the [(14)C]glutamate formed. Metabolism of the leucine carbon chain occurs in most rat
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