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Sodium hydroxybenzylphosphinate

HCID 24104
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Basic information

CAS
7492-18-4
Standard SMILES
O=[PH]([O-])C(O)c1ccccc1.[Na+]
InChIKey
UVDFAEQYRCPBRQ-UHFFFAOYSA-M
Molecular formula
C7H8NaO3P
Average molar mass
194.1 g/mol
Monoisotopic mass
194.01087539

Names & identifiers

Preferred name
Sodium hydroxybenzylphosphinate
IUPAC
sodium [hydroxy(phenyl)methyl]phosphinate
English name
alpha-Hydroxybenzylphosphinic acid sodiu
Molecular formula
C7H10NaO3P
Molecular weight
196.12

Names & synonyms

Hydroxybenzylphosphinate sodiumNSC-163897RefChem:1098803231-313-2O87RMQ5GOFSodium hydroxybenzylphosphinateNsc163897α-Hydroxybenzylphosphinic AcidSodium α-hydroxybenzylphosphinatesodium alpha-hydroxybenzylphosphinatealpha-Hydroxybenzylphosphinic acid sodiuSodium (hydroxy(phenyl)methyl)phosphinate
Show more names
α-Hydroxybenzylphosphinic Acid Sodium Salt(α-Hydroxybenzyl)phosphinic acid sodium saltα-Hydroxybenzylphosphinic Acid, CAS 7492-18-4

Database identifiers

CAS
7492-18-4
PubChem CID
24104
DTXSID
DTXSID801373173
Nikkaji
J278.886A

Properties

Computed structural properties

Topological polar surface area
60.4 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
3
Rotatable bonds
2
Heavy atoms
12
Formal charge
0
Complexity
137

Physicochemical properties

FDA UNII
87 RMQ5GOF · O87RMQ5GOF
Symbol(GHS)
7 · GHS07
Signal word
Warning
Hazard statements
319 · H319-H335-H315
Precautionary statements
264 · P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
REACH Registrations
Active

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Safety data

Signal word
Warning
Symbol(GHS)
GHS07
Hazard statements
H319-H335-H315
REACH Registrations
Active
Precautionary statements
P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362

Chemistry & industry

Applications · 1 item

UsesThe Na salt of α-hydroxybenzylphosphinic acid (Phos) is a prototype. It is harmless. Like insulin, it promotes the formation of glycogen in the isolated rat diaphragm in oxygenated glucose-Ringer solution and decreases the breakdown of glycogen provoked by adrenaline in the diaphragm preparation.

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Compound notes

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