Passa al contenuto
Merck
Tutte le immagini(1)

Documenti fondamentali

Visualizza tutta la documentazione

06711

Sigma-Aldrich

D-(−)-Citramalic acid lithium salt

≥95.0% (GC)

Sinonimo/i:

(R)-2-Hydroxy-2-methylsuccinic acid lithium salt, D-(−)-2-Methylmalic acid lithium salt

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

About This Item

Formula empirica (notazione di Hill):
C5H8O5 · xLi+
Numero CAS:
6236-10-8
Peso molecolare:
148.11 (free acid basis)
Beilstein:
1723818
Codice UNSPSC:
12352204
NACRES:
NA.32
Saggio:
≥95.0% (GC)
4-9% (Lithium, ICP)
Stato:
powder or crystals

Livello qualitativo

100

Saggio

≥95.0% (GC)
4-9% (Lithium, ICP)

Stato

powder or crystals

Attività ottica

[α]/D -19.0±2.0°, c = 0.5 in 1 M HCl

Temperatura di conservazione

2-8°C

Stringa SMILE

C[C@@](O)(CC(O)=O)C(O)=O

InChI

1S/C5H8O5/c1-5(10,4(8)9)2-3(6)7/h10H,2H2,1H3,(H,6,7)(H,8,9)/t5-/m1/s1
XFTRTWQBIOMVPK-RXMQYKEDSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Azioni biochim/fisiol

Citramalate is a biochemical intermediate known to be involved in several aspects of bacterial metabolism, including, among others, the anaerobic metabolism of glutamate via the methylaspartate pathway of Clostridium tetanomorphum.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
BCBT5310
BCBG4793
BCBG4793V

Non trovi la versione di tuo interesse?

Se hai bisogno di una versione specifica, puoi cercare il certificato tramite il numero di lotto.

Cerca un COA

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

W Buckel et al.
Journal of bacteriology, 117(3), 1248-1260 (1974-03-01)
Two pathways are involved in the fermentation of glutamate to acetate, butyrate, carbon dioxide, and ammonia-the methylaspartate and the hydroxyglutarate pathways which are used by Clostridium tetanomorphum and Peptococcus aerogenes, respectively. Although these pathways give rise to the same products
I du Preez et al.
Tuberculosis (Edinburgh, Scotland), 93(3), 330-337 (2013-03-13)
In this study, a metabolomics research approach was used to identify new tuberculosis (TB) markers from sputum, in an attempt to better characterise the disease as well as the metabolic response of the host to Mycobacterium tuberculosis infection. After GCxGC-TOFMS
Ilana Chefetz et al.
Cell reports, 26(11), 3061-3075 (2019-03-14)
Ovarian cancer is typified by the development of chemotherapy resistance. Chemotherapy resistance is associated with high aldehyde dehydrogenase (ALDH) enzymatic activity, increased cancer "stemness," and expression of the stem cell marker CD133. As such, ALDH activity has been proposed as a
Hai Xu et al.
Journal of bacteriology, 186(16), 5400-5409 (2004-08-05)
Three leuA-like protein-coding sequences were identified in Leptospira interrogans. One of these, the cimA gene, was shown to encode citramalate synthase (EC 4.1.3.-). The other two encoded alpha-isopropylmalate synthase (EC 4.1.3.12). Expressed in Escherichia coli, the citramalate synthase was purified
D M Howell et al.
Journal of bacteriology, 181(1), 331-333 (1998-12-29)
The Methanococcus jannaschii gene MJ1392 was cloned, and its protein product was hyperexpressed in Escherichia coli. The resulting protein was purified and shown to catalyze the condensation of pyruvate and acetyl coenzyme A, with the formation of (R)-citramalate. Thus, this
Visualizza tutti i documenti correlati

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.