A0262
Lithium potassium acetyl phosphate
≥85% (elemental analysis), powder
Sinônimo(s):
Acetyl phosphate lithium potassium salt
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About This Item
Fórmula linear:
CH3COOP(O)(OK)(OLi)
Número CAS:
Peso molecular:
184.06
Beilstein:
5689718
Número CE:
Número MDL:
Código UNSPSC:
12352204
ID de substância PubChem:
NACRES:
NA.32
Preço e disponibilidade não estão disponíveis no momento.
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Nome do produto
Lithium potassium acetyl phosphate, high-energy phosphate donor
Nível de qualidade
Ensaio
≥85% (elemental analysis)
Formulário
powder
pf
>300 °C (lit.)
solubilidade
water: 25 mg/mL, clear, colorless
temperatura de armazenamento
−20°C
cadeia de caracteres SMILES
[Li+].[K+].CC(=O)OP([O-])([O-])=O
InChI
1S/C2H5O5P.K.Li/c1-2(3)7-8(4,5)6;;/h1H3,(H2,4,5,6);;/q;2*+1/p-2
chave InChI
RLQMPLKXFIXRCV-UHFFFAOYSA-L
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Aplicação
Lithium potassium acetyl phosphate:
- has been used as a substrate for CpxR (transcription factor) in x-ray crystallography to soak CpxR receiver domain (CpxRRD) crystals to obtain the phosphorylated form[1]
- may be used as a phosphate (P) donor in a study to screen a wide range of natural and synthetic organic phosphate donors with several enzymes on various hydroxyl?compounds for the improved enzymatic synthesis of phosphate monoesters[2]
- has been used to set up premixA for in vitro translation reaction[3]
Ações bioquímicas/fisiológicas
Lithium potassium acetyl phosphate is commonly used as the source for acetyl phosphate. So acetyl phosphate can be used as a suitable alternative to replace inorganic oligophosphates in phosphatase-catalyzed transphosphorylation to reduce inorganic monophosphate by-product formation.[2]
Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Dam. 1 - Repr. 2 - Skin Corr. 1B
Código de classe de armazenamento
8B - Non-combustible corrosive hazardous materials
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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