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174063-97-9

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174063-97-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174063-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,0,6 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 174063-97:
(8*1)+(7*7)+(6*4)+(5*0)+(4*6)+(3*3)+(2*9)+(1*7)=139
139 % 10 = 9
So 174063-97-9 is a valid CAS Registry Number.

174063-97-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name nonadeca-6,8-diynoic acid

1.2 Other means of identification

Product number -
Other names 6,8-NONADECADIYNOIC ACID

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:174063-97-9 SDS

174063-97-9Downstream Products

174063-97-9Relevant articles and documents

Polydiacetylene paper-based colorimetric sensor array for vapor phase detection and identification of volatile organic compounds

Eaidkong, Thichamporn,Mungkarndee, Radeemada,Phollookin, Chaiwat,Tumcharern, Gamonwarn,Sukwattanasinitt, Mongkol,Wacharasindhu, Sumrit

, p. 5970 - 5977 (2012)

Detection and identification of VOCs in their vapor phase is essential for safety and quality assessment. In this work, a novel platform of a paper-based polydiacetylene (PDA) colorimetric sensor array is prepared from eight diacetylene monomers, six of which are amphiphilic and the other two are bolaamphiphilic. To fabricate the sensors, monomers are coated onto a filter paper surface using the drop-casting technique and converted to PDAs by UV irradiation. The PDA sensors show solvent induced irreversible color transition upon exposure to VOC vapors. When combined into a sensing array, the color change pattern as measured by RGB values and statistically analyzed by principal component analysis (PCA) is capable of distinguishing 18 distinct VOCs in the vapor phase. The PCA score and loading plots also allow the reduction of the sensing elements in the array from eight to three PDAs that are capable of classifying 18 VOCs. Utilizing an array containing only two PDAs, various types of automotive fuels including gasoline, gasohol and diesel are successfully classified. The Royal Society of Chemistry 2012.

Reversible color changes in lamella hybrids of poly(diacetylenecarboxylates) incorporated in layered double hydroxide nanosheets

Itoh, Toshio,Shlchi, Tetsuya,Yui, Tatsuto,Takahashi, Hiroki,Inui, Yoshihisa,Takagi, Katsuhiko

, p. 3199 - 3206 (2008/03/14)

The present study is an investigation of a reversible thermal color change induced in lamella hybrids of poly(diacetylenecarboxylates) incorporated in layered double hydroxide (LDH) nanosheets. These poly-[m,n]/ LDH hybrids prepared by the photo- or ?3-ray-induced polymerization of diacetylenecarboxylates, i.e., CH3-(CH2) m-1Ca??C-Ca??C(CH2)n-1CO 2- (mono-[m,n]), and intercalated in LDH lamella sheets, were observed to develop colors ranging from yellow to blue. The change in color was found to depend greatly on the alkyl carbon numbers of the mono-[m,n] (m,n = 10,11; 5,11; 10,5; 16,1) values. Moreover, the conformational alignment of the mono-[m,n] within the LDH was observed to be a crucial factor in color development, which was greatly affected by the intercalation degrees and extent of poly(ene-yne) linkage elongation of the polymers. For the poly-[m,n]/LDH hybrids investigated, a reversible color change was found to occur repeatedly and remarkably for the poly-[10,11]/LDH hybrid. This color change occurred at temperatures between ca. 20 and 80?°C back and forth from purple red to bright orange, in stark contrast to the irreversible color change for poly-[10,11] without LDH. Moreover, DSC and Raman spectroscopic studies of the LDH hybrids showed that the thermochromic temperature corresponded to the phase transition temperature of 80?°C. XRD analysis also indicated that the poly-[m,n]/LDH hybrid could retain its lamella structure during such thermochromic color changes, enabling conformational recovery in the polymer chains by a cooling down of the hybrids to temperatures lower than the transition temperature, while the nonhybrid poly-[10,11] powders exhibited an irreversible color change at 60?°C, above which the polymer powder turned amorphous. ? 2005 American Chemical Society.

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