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(-)-2,3-dimethylbutane-1,2,3-tricarboxylic acid, also known as citric acid, is a tricarboxylic acid with the molecular formula C9H14O6. It is a weak organic acid that is naturally found in citrus fruits such as lemons, limes, and oranges. (-)-2,3-dimethylbutane-1,2,3-tricarboxylic acid is characterized by its three carboxylic acid functional groups and its versatile chemical structure, which contributes to its wide range of applications across different industries.

2385-74-2

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2385-74-2 Usage

Uses

Used in Food Industry:
(-)-2,3-dimethylbutane-1,2,3-tricarboxylic acid is used as a food additive to impart a sour taste to various foods and beverages. Its natural occurrence and ability to enhance flavors make it a popular ingredient in the culinary world.
Used in Cleaning Products:
Citric acid is utilized as a cleaning agent due to its ability to remove stains, rust, and mineral deposits. Its effectiveness in breaking down tough dirt and grime makes it a common component in household and industrial cleaning solutions.
Used in Pharmaceutical Products:
(-)-2,3-dimethylbutane-1,2,3-tricarboxylic acid is used in the pharmaceutical industry for its ability to chelate metal ions, which helps stabilize medications and improve their absorption in the body.
Used in Cosmetic Products:
In the cosmetic industry, citric acid is employed for its exfoliating and brightening properties. It helps remove dead skin cells and even out skin tone, making it a valuable ingredient in skincare formulations.
Used in Biotechnology:
(-)-2,3-dimethylbutane-1,2,3-tricarboxylic acid is also used in biotechnological applications, such as in the production of bioplastics and as a building block for the synthesis of other organic compounds. Its versatility and biocompatibility make it a promising component in green chemistry and sustainable product development.

Check Digit Verification of cas no

The CAS Registry Mumber 2385-74-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2385-74:
(6*2)+(5*3)+(4*8)+(3*5)+(2*7)+(1*4)=92
92 % 10 = 2
So 2385-74-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O6/c1-8(2,6(12)13)9(3,7(14)15)4-5(10)11/h4H2,1-3H3,(H,10,11)(H,12,13)(H,14,15)

2385-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethylbutane-1,2,3-tricarboxylic acid

1.2 Other means of identification

Product number -
Other names EINECS 219-192-4

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:2385-74-2 SDS

2385-74-2Relevant academic research and scientific papers

Polyethylene Glycols as Efficient Catalysts for the Oxidation of Bicyclic Monoterpenes by Ceric Ammonium Nitrate in Acetonitrile under Acid-Free Conditions: Kinetic and Mechanistic Approach

Rajitha,Shylaja,Rajanna,Yadagiri

, p. 383 - 396 (2018/03/30)

Polyethylene glycols (PEG) acts as efficient catalysts for the oxidation of bicyclic monoterpenes such as borneol, isoborneol, and camphor by ceric ammonium nitrate (CAN), a laboratory desktop reagent, in acetonitrile medium under mineral acid-free conditions. The kinetics of the reactions revealed first-order dependence on in both [CAN] and [bicyclic terpene]. The rate of oxidation is accelerated with an increase in [PEG] linearly, which could be explained by considering PEG-bound oxidant (PEG-CAN) as more reactive species than (CAN) itself. The mechanism of oxidation in PEG media has been explained through the participation of PEG-bound oxidant (PEG-CAN) and bicyclic monoterpene in the slow step.

THE REACTION OF 3-METHYLTRICARBALLYLIC ACID WITH ACETIC ANHYDRIDE. ADDENDUM: ON FITTIG'S PRODUCT FROM ACYLATIVE DECARBOXYLATION OF CAMPHORONIC ACID

Strunz, George M.,Giguere, Pierre

, p. 204 - 205 (2007/10/02)

Two products, 2,7-dioxa-1,4,4,5-tetramethylbicyclooctane-3,6-dione (5), and 2-acetonyl-2,3,3-trimethylsuccinic anhydride (4) were identified from the base-catalysed reaction of camphoronic acid, 2(R',R" = CH3), with acetic anhydride.The former (5) is believed to be identical with the product described by Fittig and assigned an isomeric formulation.

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