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2375-06-6

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2375-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2375-06-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,7 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2375-06:
(6*2)+(5*3)+(4*7)+(3*5)+(2*0)+(1*6)=76
76 % 10 = 6
So 2375-06-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H16NO4P/c1-7(2,3)5-6-11-12(8,9)10-4/h5-6H2,1-4H3

2375-06-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(trimethylazaniumyl)ethyl phosphate

1.2 Other means of identification

Product number -
Other names hydroxide methyl hydrogen phosphate innersalt

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2375-06-6 SDS

2375-06-6Downstream Products

2375-06-6Relevant articles and documents

FTIR-spectroscopic characterization of phosphocholine-headgroup model compounds

Pohle,Gauger,Fritzsche,Rattay,Selle,Binder,B?hlig

, p. 463 - 467 (2001)

The polar headgroups are an important molecular subregion of phospholipids since they mediate a substantial part of the interactions emerging with other constituents of biological membranes, be it inherent macromolecules (proteins) or water as forming the natural environment. FTIR spectroscopy is well proven for characterizing aspects of weak interactions, above all hydrogen bonding. We have used this method to study solid deposits of a number of selected lipid models, such as choline, acetylcholine and methylphosphocholine (MePC), and compared them with the common phospholipid dimyristoylglycero-phosphocholine (DMPC), at different degrees of hydration, which were varied via relative humidity (RH). At low RHs, only MePC and DMPC take up considerable amounts of water, thus elucidating the essential role of phosphate groups in the first stages of lipid hydration. The progress of PC-headgroup hydration can be sensitively monitored by the wavenumber decrease of the band owing to antisymmetric PO2- stretching vibration. Concomitant variations of the spectral parameters of vCH bands of MePC reveal that conformational changes may simultaneously occur in the headgroup. Surprisingly to us, the model compounds display qualitative differences in the appearance of their vCH bands, which are most probably a result of substituent effects.

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