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Merck
CN

P6502

Phosphocreatine disodium salt hydrate

~98%

Synonym(s):

N-(Imino[phosphonoamino]methyl)-N-methylglycine

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About This Item

Linear Formula:
C4H8N3O5PNa2 · x H2O
CAS Number:
19333-65-4
Molecular Weight:
255.08 (anhydrous basis)
UNSPSC Code:
12352200
PubChem Substance ID:
329820245
EC Number:
213-074-6
MDL number:
MFCD00150191

Key Documents

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Product Name

Phosphocreatine disodium salt hydrate, ~98%

InChI key

KZVYPOKBYRXZKS-UHFFFAOYSA-L

InChI

1S/C4H10N3O5P.2Na.H2O/c1-7(2-3(8)9)4(5)6-13(10,11)12;;;/h2H2,1H3,(H,8,9)(H4,5,6,10,11,12);;;1H2/q;2*+1;/p-2

SMILES string

O.[Na+].[Na+].CN(CC(O)=O)C(=N)NP([O-])([O-])=O

assay

~98%

storage temp.

−20°C

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Biochem/physiol Actions

Phosphocreatine, a high-energy phosphate reservoir in vertebrate and some invertebrate muscles, provides phosphate for ADP-ATP conversion.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
092H5634
074H5747
060H5629
123H5711
102H5608

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Justin L Sparks et al.
Cell, 176(1-2), 167-181 (2019-01-01)
Covalent DNA-protein cross-links (DPCs) impede replication fork progression and threaten genome integrity. Using Xenopus egg extracts, we previously showed that replication fork collision with DPCs causes their proteolysis, followed by translesion DNA synthesis. We show here that when DPC proteolysis

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