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7217-25-6

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7217-25-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7217-25-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,1 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7217-25:
(6*7)+(5*2)+(4*1)+(3*7)+(2*2)+(1*5)=86
86 % 10 = 6
So 7217-25-6 is a valid CAS Registry Number.

7217-25-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Acetone-1,3-13C2

1.2 Other means of identification

Product number -
Other names Propanone-1,3-13C2

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:7217-25-6 SDS

7217-25-6Upstream product

7217-25-6Relevant articles and documents

Cascade reactions for the continuous and selective production of isobutene from bioderived acetic acid over zinc-zirconia catalysts

Crisci, Anthony J.,Dou, Herui,Prasomsri, Teerawit,Romn-Leshkov, Yuriy

, p. 4196 - 4200 (2014)

Bio-oil (obtained from biomass fast pyrolysis) contains a high concentration of acetic acid, which causes problems related to its storage and handling. Acetic acid was upgraded directly to isobutene over a ZnxZryOz binary metal oxide. The reaction proceeds via a three-step cascade involving ketonization, aldol condensation, and C-C hydrolytic bond cleavage reactions, which was corroborated by isotopic labeling studies. Separately, ZnO and ZrO2 are incapable of producing isobutene from either acetic acid or acetone. In contrast, under optimal conditions, a Zn2Zr8Oz catalyst generates a ca. 50% isobutene yield, which corresponds to 75% of the theoretical maximum. Spectroscopic investigations revealed that a balanced concentration of acid and base sites is required to maximize isobutene yields.

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