645-84-1 Usage
Phosphorus-containing compound
Contains a phosphate group (PO4) bonded to a carbon chain.
Positively charged
Trimethylammonium group (N+(CH3)3)
Negatively charged
Phosphate group (PO4-)
Buffer
Used to maintain a stable pH level in biochemical and pharmaceutical solutions.
Stabilizer
Helps maintain the stability and integrity of biomolecules in various applications.
Drug production
Component in the synthesis of certain pharmaceutical compounds.
Cosmetic component
Included in some cosmetic formulations for its stabilizing and buffering properties.
Environmental remediation
Potential use in the treatment and cleanup of contaminated environments, such as water and soil.
Catalyst
2-(trimethylammonio)ethyl hydrogen phosphate has been studied for its potential as a catalyst in organic synthesis reactions, promoting and accelerating chemical transformations.
Check Digit Verification of cas no
The CAS Registry Mumber 645-84-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,4 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 645-84:
(5*6)+(4*4)+(3*5)+(2*8)+(1*4)=81
81 % 10 = 1
So 645-84-1 is a valid CAS Registry Number.
645-84-1Relevant articles and documents
Conjugated polyelectrolyte based real-time fluorescence assay for phospholipase C
Liu, Yan,Ogawa, Katsu,Schanze, Kirk S.
, p. 150 - 158 (2008/09/17)
A fluorescence turnoff assay for phospholipase C (PLC) from Clostridium perfringens is developed based on the reversible interaction between the natural substrate, phosphatidylcholine, and a fluorescent, water-soluble conjugated polyelectrolyte (CPE). The fluorescence intensity of the CPE in water is increased substantially by the addition of the phospholipid due to the formation of a CPE-lipid complex. Incubation of the CPE-lipid complex with the enzyme PLC causes the fluorescence intensity to decrease (turnoff sensor); the response arises due to PLC-catalyzed hydrolysis of the phosphatidylcholine, which effectively disrupts the CPE-lipid complex. The PLC assay operates with phospholipid substrate concentrations in the micromolar range, and the analytical detection limit for PLC is 2+ and inhibition by EDTA and fluoride ion are demonstrated using the optimized sensor.