21273-38-1 Usage
Description
2-Phenoxyethyl-1,1-D2 Alcohol, also known as 2-Phenoxyethanol (P297900), is a deuterated compound with the molecular formula C8D7O2. It is a colorless liquid with a faint, aromatic odor and is commonly used as a preservative in the cosmetics industry. Additionally, it serves as an anesthetic in aquaculture and fisheries, making it a versatile compound with applications in various fields.
Uses
Used in Cosmetics Industry:
2-Phenoxyethyl-1,1-D2 Alcohol is used as a preservative for [application type] in the cosmetics industry to [application reason] extend the shelf life of products and prevent the growth of microorganisms, ensuring the safety and efficacy of cosmetic formulations.
Used in Aquaculture and Fisheries:
In the aquaculture and fisheries industry, 2-Phenoxyethyl-1,1-D2 Alcohol is used as an anesthetic for [application type] to [application reason] immobilize fish during transportation and handling, reducing stress and mortality rates, and improving the overall welfare of the animals.
Check Digit Verification of cas no
The CAS Registry Mumber 21273-38-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,7 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21273-38:
(7*2)+(6*1)+(5*2)+(4*7)+(3*3)+(2*3)+(1*8)=81
81 % 10 = 1
So 21273-38-1 is a valid CAS Registry Number.
21273-38-1Relevant articles and documents
Stereochemistry of the conversion of 2-phenoxyethanol into phenol and acetaldehyde by Acetobacterium sp.
Speranza, Giovanna,Mueller, Britta,Orlandi, Maximilian,Morelli, Carlo F.,Manitto, Paolo,Schink, Bernhard
, p. 2629 - 2636 (2007/10/03)
The conversion of 2-phenoxyethanol to phenol and acetate by the anaerobic bacterium Acetobacterium sp. strain LuPhet1 proceeds through acetaldehyde with concomitant migration of a H-atom from C(1) to C(2) of the glycolic moiety. Separate feeding experiments with (R)- and (S)-2-phenoxy(1- 2H)ethanol, prepared via chemoenzymatic syntheses, indicate that the H-atom involved in the 1,2-shift is the pro-S one of the enantiotopic couple of the alcohol function.
DISSOZIATIVE IONISIERUNG VON 2-TRIMETHYLSILYL-1-PHENOXYETHAN, NACHWEIS DES NICHT-KLASSISCHEN ETHYLEN-TRIMETHYLSILANIUM-IONS IN DER GASPHASE
Ciommer, Bernhard,Schwarz, Helmut
, p. 319 - 328 (2007/10/02)
The mass spectrometric investigation of specifically deuterium and 13C labelled 2-trimethylsilyl-1-phenoxyethanes proves that the dissociative ionization of β-silyl-substituted ethane derivatives (loss of PhO., p-CH3C6H4O. and C4H9s
