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54763

Supelco

L-Serine

certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Synonim(y):

(S)-2-Amino-3-hydroxypropionic acid

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About This Item

Wzór liniowy:
HOCH2CH(NH2)CO2H
Numer CAS:
56-45-1
Masa cząsteczkowa:
105.09
Beilstein:
1721404
Numer WE:
200-274-3
Numer MDL:
MFCD00064224
Kod UNSPSC:
41116107
eCl@ss:
32160406
Identyfikator substancji w PubChem:
329758055
NACRES:
NA.24

klasa czystości

certified reference material
TraceCERT®

Poziom jakości

300

linia produktu

TraceCERT®

klasy chemiczne analitów

amino acids, peptides, proteins

producent / nazwa handlowa

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

metody

HPLC: suitable
gas chromatography (GC): suitable

kolor

white

mp

222 °C (dec.) (lit.)

Zastosowanie

food and beverages

format

neat

ciąg SMILES

N[C@@H](CO)C(O)=O

InChI

1S/C3H7NO3/c4-2(1-5)3(6)7/h2,5H,1,4H2,(H,6,7)/t2-/m0/s1

Klucz InChI

MTCFGRXMJLQNBG-REOHCLBHSA-N

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Opis ogólny

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.

Check out the entire portfolio of our amino acids certified reference materials (CRM)

Zastosowanie

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Działania biochem./fizjol.

Precursor of glycine by serine hydroxymethyltransferase.

Opakowanie

Bottomless glass bottle. Contents are inside inserted fused cone.

Informacje prawne

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
This page may contain text that has been machine translated.

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Środki ochrony indywidualnej

Eyeshields, Gloves, type N95 (US)

Wybierz jedną z najnowszych wersji:

Certyfikaty analizy (CoA)

Lot/Batch Number
BCCD1580
BCCB8411
BCBR3866V
BCBH4260V
BCBB4612

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Jeśli potrzebujesz konkretnej wersji, możesz wyszukać konkretny certyfikat według numeru partii lub serii.

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Miyoshi Haruta et al.
Science (New York, N.Y.), 343(6169), 408-411 (2014-01-25)
Plant cells are immobile; thus, plant growth and development depend on cell expansion rather than cell migration. The molecular mechanism by which the plasma membrane initiates changes in the cell expansion rate remains elusive. We found that a secreted peptide
Kenji Hashimoto et al.
Progress in neuro-psychopharmacology & biological psychiatry, 29(5), 767-769 (2005-06-09)
Several lines of evidence suggest that D-serine, an endogenous agonist of the glycine site on the NMDA receptors, might play a role in the pathophysiology of schizophrenia. The purpose of this study was to determine whether levels of D- and
Cedric Cagliero et al.
Nucleic acids research, 41(12), 6058-6071 (2013-05-02)
To fit within the confines of the cell, bacterial chromosomes are highly condensed into a structure called the nucleoid. Despite the high degree of compaction in the nucleoid, the genome remains accessible to essential biological processes, such as replication and
Hisaaki Shinohara et al.
Science (New York, N.Y.), 344(6185), 760-764 (2014-05-17)
A switchlike response in nuclear factor-κB (NF-κB) activity implies the existence of a threshold in the NF-κB signaling module. We show that the CARD-containing MAGUK protein 1 (CARMA1, also called CARD11)-TAK1 (MAP3K7)-inhibitor of NF-κB (IκB) kinase-β (IKKβ) module is a
Tom J de Koning et al.
The Biochemical journal, 371(Pt 3), 653-661 (2003-01-22)
The amino acid L-serine, one of the so-called non-essential amino acids, plays a central role in cellular proliferation. L-Serine is the predominant source of one-carbon groups for the de novo synthesis of purine nucleotides and deoxythymidine monophosphate. It has long
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Protokoły

GC Analysis of Amino Acids (as TBDMS Derivatives) on SLB®-5ms (20 m x 0.18 mm I.D., 0.18 μm), Fast GC Analysis

Separation of L-Alanine; Glycine; L-Valine; L-Leucine; L-Isoleucine; L-Proline; L-Methionine; L-Serine; L-Threonine; L-Phenylalanine; L-Aspartic acid; L-4-Hydroxyproline; L-Cysteine; L-Glutamic acid; L-Asparagine; L-Lysine; L-Glutamine; L-Histidine; L-Tyrosine; L-Tryptophan; L-Cystine

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