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3-methylbutane-1,2,3-tricarboxylic acid is a complex organic compound with the molecular formula C7H10O6. It is a tricarboxylic acid, meaning it contains three carboxylic acid groups. The compound is characterized by a 3-methylbutane backbone, which is a branched chain of five carbon atoms with a methyl group attached to the third carbon. The three carboxylic acid groups are attached to the first, second, and third carbon atoms of the chain, respectively. 3-methylbutane-1,2,3-tricarboxylic acid is not commonly found in nature but can be synthesized for various chemical and industrial applications, such as in the production of certain polymers or as an intermediate in the synthesis of other complex molecules. Due to its unique structure, it may also be of interest in the study of organic chemistry and the development of new materials.

77370-41-3

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77370-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77370-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,7 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77370-41:
(7*7)+(6*7)+(5*3)+(4*7)+(3*0)+(2*4)+(1*1)=143
143 % 10 = 3
So 77370-41-3 is a valid CAS Registry Number.

77370-41-3SDS

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 3-methyl-1,2,3-butanetricarboxylic acid

1.2 Other means of identification

Product number -
Other names γ-Methyl-butan-α.β.γ-tricarbonsaeure

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:77370-41-3 SDS

77370-41-3Downstream Products

77370-41-3Relevant academic research and scientific papers

Glass-forming properties of 3-methylbutane-1,2,3-tricarboxylic acid and its mixtures with water and pinonic acid

Dette, Hans P.,Qi, Mian,Schroeder, David C.,Godt, Adelheid,Koop, Thomas

, p. 7024 - 7033 (2014)

3-Methylbutane-1,2,3-tricarboxylic acid (3-MBTCA) is an atmospheric oxidation product of α-pinene and has been identified as the most relevant tracer compound for atmospheric terpene secondary organic aerosol (SOA) particles. Little is known, however, of its physicochemical properties such as water solubility and phase state (e.g., liquid, crystalline, glassy). To gain knowledge, we synthesized 3-MBCTA from methyl 2-methylpropanoate and dimethyl maleate via a Michael addition and subsequent hydrolysis with 78% overall yield. It was found that 3-MBTCA transforms into anhydrides upon melting at T m = 426 ± 1 K, thus preventing a determination of the glass transition temperature Tg by differential scanning calorimetry (DSC) through melting and subsequent cooling. Therefore, we designed the novel technique MARBLES (metastable aerosol by low temperature evaporation of solvent) for transferring a substance into a glassy state without heating. In MARBLES an aqueous solution is atomized into wet aerosol particles that are subsequently dried in several diffusion dryers resulting in glass formation of the residual particles for several solutes. The glassy aerosol particles are collected in an impactor until enough mass has accumulated that the sample's Tg can be determined by DSC. Using this method, the glass transition temperature of 3-MBTCA was found to be Tg ≈ 305 ± 2 K. Moreover, we have determined the glass transition Tg' of the maximal freeze-concentrated aqueous solution of 3-MBTCA, and Tg of mixtures of 3-MBTCA with water and pinonic acid. The latter data indicate a dependence of Tg upon the atomic oxygen-to-carbon ratio of the mixture, with implications for parametrizing the glass-forming behavior of α-pinene SOA particles in the atmosphere.

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