75-96-7 Hazards Identification
Pictogram(s):
Signal:
Danger
GHS Hazard Statements:
H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
Precautionary Statement Codes:
P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501
Hazard Classes and Categories:
Skin Corr. 1B (100%)
Hazards Summary:
No reproductive or general toxicity observed in oral study of rats at doses up 400 ppm in drinking water; [NTP] Causes effects on fluid and food intake, changes in liver and kidney weights, hematuria, other changes of the kidney, ureter, and bladder, and changes in blood serum composition in 14-day constant oral studies of rats; [RTECS] Causes burns; Inhalation may cause corrosive injuries to upper respiratory tract; [Sigma-Aldrich MSDS]
75-96-7 Usage
Uses
Used in Polymerization Industry:
Tribromoacetic acid is used as a catalyst for polymerization processes, enhancing the reaction rate and improving the overall efficiency of the process.
Used as a Brominating Agent:
Tribromoacetic acid is employed as a brominating agent in various chemical reactions, where it can transfer bromine atoms to other molecules, leading to the formation of brominated compounds. This property makes it useful in the synthesis of various organic and inorganic compounds.
Reference:
W. J. Szczepek, Pol. J. Chem. 55, 709 (1981).
Check Digit Verification of cas no
The CAS Registry Mumber 75-96-7 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75-96:
(4*7)+(3*5)+(2*9)+(1*6)=67
67 % 10 = 7
So 75-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C2HBr3O2/c3-2(4,5)1(6)7/h(H,6,7)
75-96-7Relevant academic research and scientific papers
Liquid-phase oxidation of bromovinyl compounds with molecular oxygen
Bayatyan,Bayatyan,Saakyan
, p. 1849 - 1852 (2008/02/08)
Liquid-phase oxidation of bromovinyl compounds with the aim to obtain the corresponding α-bromo acids was studied.
EVIDENCE OF ESTERIFICATION DURING THE OXIDATION OF SOME AROMATIC ALDEHYDES BY CHROMIUM (VI) IN ACID MEDIUM AND THE MECHANISM OF THE OXIDATION PROCESS
Gupta, Kalyan Kali Sen,Dey, Sanghamitra,Gupta, Shipra Sen,Adhikari, Mrityunjoy,Banerjee, Amalendu
, p. 2431 - 2444 (2007/10/02)
The oxidation kinetics of some aromatic aldehydes by chromium (VI) have been studied in perchloric acid medium.Kinetic and spectrophotometric results indicate the formation of a 1:1 intermediate ester between the reactive chromium (VI) species and protonated benzaldehyde.The rate is directly proportional to the square of hydrogen ion concentrations.The rate of oxidation decreases with the presence of electron donating groups and increases with electron withdrawing groups on the aromatic ring.The activation parameters associated with the rate determining step and the thermodynamic values associated with the equilibrium step have been computed.An attempt has been made to compare the results obtained with those for the oxidations of some aliphatic aldehydes which do not have enolizable hydrogen.
MERCURATION OF 2-ALKYL-1,3-DIOXOLAN-2-YLIUM SALTS: NEW METHOD FOR THE SYNTHESIS OF α-MERCURIO CARBOXYLIC ACIDS
Boev, V. I.,Dombrovskii, A. V.
, p. 1927 - 1930 (2007/10/02)
In the mercuration of 2-alkyl-1,3-dioxolan-2-ylium perchlorates with mercury acetate of trifluoroacetate high yileds of mono-, di-, and tri-α-mercurio derivatives of carboxylic acids wre obtained, depenging on the proportions of the reacting substrates.
