14300
Betaine monohydrate
≥99.0% (NT)
Synonyme(s) :
1-carboxy-n,n,n-trimethylmethanaminium hydroxide, 2-(trimethylammonio)acetate hydrate, glycine betaine hydrate
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54,10 €
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187,00 €
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100 G
54,10 €
500 G
187,00 €
About This Item
Formule linéaire :
(CH3)3N+CH2COO- · H2O
Numéro CAS:
Poids moléculaire :
135.16
Beilstein:
3626258
Numéro CE :
Numéro MDL:
Code UNSPSC :
51171529
ID de substance PubChem :
Nomenclature NACRES :
NA.25
54,10 €
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Niveau de qualité
Essai
≥99.0% (NT)
Forme
solid
Solubilité
H2O: 0.1 g/mL, clear, colorless
Température de stockage
2-8°C
Chaîne SMILES
O.C[N+](C)(C)CC([O-])=O
InChI
1S/C5H11NO2.H2O/c1-6(2,3)4-5(7)8;/h4H2,1-3H3;1H2
Clé InChI
NJZRLXNBGZBREL-UHFFFAOYSA-N
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Application
Betaine monohydrate:
- is suitable for use to improve the PCR amplification of GC-rich DNA sequences by reducing the formation of secondary structure caused by GC-rich regions[1]
- is suitable for use as a component of PCR reaction mixture[2][3]
- is suitable for use in a study to identify yield enhancers of PCR[4]
- has been used to study nitrogen balance and nutrient digestibility in piglets fed diets deficient in methionine and low in compatible osmolytes[5]
- has also been used to compare the effects of pressure on three layered hydrates[6]
Actions biochimiques/physiologiques
End-product of oxidative metabolism of choline, betaine is a general methyl donor, in particular in a minor pathway of methionine biosynthesis. It is used to treat homocystinuria, which is a defect in the major pathway of methionine biosynthesis.[7]
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 1
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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Les clients ont également consulté
Meike Eklund et al.
Archives of animal nutrition, 60(4), 289-300 (2006-08-23)
A balance experiment was carried out to investigate the effects of betaine monohydrate (BET) or betaine derived from condensed molasses solubles (CMS) as a substitute for methionine and choline on nitrogen (N) balance and total tract nutrient digestibility in weaned
Cletus Nunes et al.
Journal of pharmaceutical sciences, 93(1), 38-47 (2003-12-04)
The objectives were (1). to perform solid-state characterization of anhydrous betaine (A) and betaine monohydrate (M), (2). to develop a pressure differential scanning calorimetric (DSC) technique for the quantification of M when present as a minor component in a mixture
M Kovárová et al.
Nucleic acids research, 28(13), E70-E70 (2000-06-28)
Tetramethylammonium (TMA) chloride, dimethyl sulfoxide and formamide are known to increase, under certain conditions, the specificity and efficiency of the polymerase chain reaction (PCR). We compared the ability of several TMA derivatives and some other reagents to increase the specificity
Theodore Spilker et al.
Journal of clinical microbiology, 50(9), 3010-3015 (2012-07-13)
The genus Achromobacter currently is comprised of seven species, including Achromobacter xylosoxidans, an opportunistic and nosocomial pathogen that displays broad-spectrum antimicrobial resistance and is recognized as causing chronic respiratory tract infection in persons with cystic fibrosis (CF). To enable strain
Russell D L Johnstone et al.
Acta crystallographica. Section B, Structural science, 65(Pt 6), 731-748 (2009-11-20)
We report the effect of pressure on the crystal structures of betaine monohydrate (BTM), L-cysteic acid monohydrate (CAM) and S-4-sulfo-L-phenylalanine monohydrate (SPM). All three structures are composed of layers of zwitterionic molecules separated by layers of water molecules. In BTM
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