73489
L-α-Neopentylglycine
≥98.0% (TLC)
Synonym(s):
γ-Methyl-L-leucine, (S)-2-Amino-4,4-dimethylpentanoic acid, L-γ-Methylleucine
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About This Item
Empirical Formula (Hill Notation):
C7H15NO2
CAS Number:
Molecular Weight:
145.20
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
≥98.0% (TLC)
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
application(s)
peptide synthesis
SMILES string
[H][C@](N)(CC(C)(C)C)C(O)=O
InChI
1S/C7H15NO2/c1-7(2,3)4-5(8)6(9)10/h5H,4,8H2,1-3H3,(H,9,10)/t5-/m0/s1
InChI key
LPBSHGLDBQBSPI-YFKPBYRVSA-N
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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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J L Fauchère et al.
International journal of peptide and protein research, 18(3), 249-255 (1981-09-01)
The modified Strecker synthesis of Patel & Worsley was combined with an enzymatic deamidation in the final step, to produce the title compound. The amino acid is a member of the family of the "fat" amino-acids with high lipophilicity and
Xuejing Yu et al.
The FEBS journal, 281(1), 391-400 (2013-11-12)
Branched-chain amino acid aminotransferase (BCAT) plays a key role in the biosynthesis of hydrophobic amino acids (such as leucine, isoleucine and valine), and its substrate spectrum has not been fully explored or exploited owing to the inescapable restrictions of previous
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