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10321-14-9

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10321-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10321-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,2 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10321-14:
(7*1)+(6*0)+(5*3)+(4*2)+(3*1)+(2*1)+(1*4)=39
39 % 10 = 9
So 10321-14-9 is a valid CAS Registry Number.

10321-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,3-trifluoro-2,2-dihydroxypropanoic acid

1.2 Other means of identification

Product number -
Other names 3,3,3-trifluoro-2,2-dihydroxy-propionic 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:10321-14-9 SDS

10321-14-9Upstream product

10321-14-9Relevant articles and documents

Rate constants and C–C bond scission ratios for hydrolysis of 2,2,3-trifluoro-3-(trifluoromethyl)oxirane determined by means of a closed-circulation reactor

Kutsuna, Shuzo

, p. 109 - 118 (2018)

The hydrolysis rate constant of 2,2,2-trifluoro-3-(trifluoromethyl)oxirane (hexafluoropropene oxide; HFPO), a versatile precursor of fluorinated chemicals, was determined at 279–307 K, and the rate of hydrolysis was used to estimate the tropospheric lifetime of HFPO with respect to hydrolysis in clouds or uptake by the ocean. The low solubility of HFPO in water made it difficult to determine the hydrolysis rate constant because of mass-transfer limitation between the gas and liquid. A closed-circulation reactor was used to measure the rate of decrease of the partial pressure of HFPO while an HFPO-air mixture flowed over a stirred test solution under various experimental conditions. The rate of hydrolysis increased as the OH? concentration increased in an aqueous NaOH solution but was almost independent of the H2SO4 concentration in aqueous H2SO4 solutions. Much scissioning of C–C bonds in HFPO produced carbon monoxide and trifluoroacetate in aqueous NaOH, but similar scissioning did not in water or aqueous H2SO4. The first-order rate constant for the pH-independent hydrolysis (kwater in s?1), the bimolecular rate constant for the hydroxide-catalyzed hydrolysis, and the temperature dependence of these parameters were estimated by simultaneously fitting equations based on a two-film model to the time series of HFPO partial pressures under different experimental conditions. The equations included the rate constants as common parameters. The product of kwater and the Henry's law constant, KH (M Pa?1), at a temperature of T (K) was determined to be kwater × KH = 3.7 × 10?11 exp[?3300 × (T?1 ? 1/298.2)]. The tropospheric lifetime of HFPO estimated using this equation indicates that removal of HFPO via hydrolysis in clouds is probably not a substantial sink of HFPO and suggests that, in the absence of other atmospheric sinks of HFPO, hydrolysis of HFPO in the ocean would be the major sink of HFPO.

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