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M7378

Sigma-Aldrich

O-Methyl-DL-serine

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About This Item

Empirical Formula (Hill Notation):
C4H9NO3
CAS Number:
19794-53-7
Molecular Weight:
119.12
MDL number:
MFCD00037773
UNSPSC Code:
12352202
PubChem Substance ID:
24897157
NACRES:
NA.26

Assay

≥98.0% (TLC)

form

powder

color

white to off-white

SMILES string

COCC(N)C(O)=O

InChI

1S/C4H9NO3/c1-8-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)

InChI key

KNTFCRCCPLEUQZ-UHFFFAOYSA-N

Biochem/physiol Actions

O-Methyl-DL-serine is a derivative of L-serine that has an affects E. Coli growth.

Storage Class Code

13 - Non 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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

M7378-VAR:
M7378-250MG:
M7378-25G:
M7378-1G:
M7378-5G:
M7378-BULK:

Certificates of Analysis (COA)

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C Y Shiau et al.
Biochemistry, 36(29), 8798-8806 (1997-07-22)
L-delta-(alpha-Aminoadipoyl)-L-cysteinyl-D-valine (ACV) synthetase is probably the simplest known peptide synthetase in terms of the number of reactions catalyzed. In the "thiol-template" proposal for nonribosomal peptide synthesis, a key step is transfer of aminoacyl groups derived from the substrates to enzyme-bound
K D Schnackerz et al.
Biochemistry, 34(38), 12152-12160 (1995-09-26)
The O-acetylserine sulfhydrylase (OASS) reaction has been studied using a number of spectral probes including UV--visible, fluorescence, circular dichroism, and 31P NMR spectroscopy. The addition of L-cysteine, L-alanine, and glycine to OASS results in a shift in lambda max of
Birgit Geueke et al.
Applied microbiology and biotechnology, 74(6), 1240-1247 (2007-02-07)
A screening of soil samples for D-amino acid oxidase (D-AAO) activity led to the isolation and identification of the gram-positive bacterium Arthrobacter protophormiae. After purification of the wild-type D-AAO, the gene sequence was determined and designated dao. An alignment of
Taro Yamada et al.
Biochemistry, 42(44), 12854-12865 (2003-11-05)
SDH (L-serine dehydratase, EC 4.3.1.17) catalyzes the pyridoxal 5'-phosphate (PLP)-dependent dehydration of L-serine to yield pyruvate and ammonia. Liver SDH plays an important role in gluconeogenesis. Formation of pyruvate by SDH is a two-step reaction in which the hydroxyl group
Taro Yamada et al.
Biochimica et biophysica acta, 1780(5), 809-818 (2008-03-18)
SDH (l-serine dehydratase, EC 4.3.1.17) is a pyridoxal-5'-phosphate (PLP)-dependent enzyme that catalyzes dehydration of l-Ser/Thr to yield pyruvate/ketobutyrate and ammonia. A SDH isoform (cSDH) found in human cancer cell lines has relatively low catalytic activity in comparison with the liver
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