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Phthalic Acid (Ring-D4) is a synthetic aromatic dicarboxylic acid that is commonly used as a precursor in the production of various chemicals and materials. It is characterized by its ring structure and deuterium labeling, which provides unique properties and applications in different industries.

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  • 87976-26-9 Structure
  • Basic information

    1. Product Name: PHTHALIC ACID (RING-D4)
    2. Synonyms: PHTHALIC-3,4,5,6-D4 ACID;PHTHALIC ACID (RING-D4);PHTHALIC-D4 ACID;PHTHALIC-D4 ACID, 98 ATOM % D;1,2-Benzene-3,4,5,6-d4-dicarboxylic acid;phthalic acid-phenyl-d4;Phthalic Acid-d4;1,2-(Benzene-d4)dicarboxylic Acid
    3. CAS NO:87976-26-9
    4. Molecular Formula: C8H6O4
    5. Molecular Weight: 170.16
    6. EINECS: N/A
    7. Product Categories: Aromatics;Isotope Labelled Compounds;Miscellaneous Reagents
    8. Mol File: 87976-26-9.mol
  • Chemical Properties

    1. Melting Point: 210-211 °C(lit.)
    2. Boiling Point: 378.3°C at 760 mmHg
    3. Flash Point: 196.7°C
    4. Appearance: /
    5. Density: 1.486g/cm3
    6. Vapor Pressure: 2.14E-06mmHg at 25°C
    7. Refractive Index: 1.617
    8. Storage Temp.: Hygroscopic, -20°C Freezer, Under inert atmosphere
    9. Solubility: DMSO (Slightly), Methanol (Slightly)
    10. Stability: Hygroscopic
    11. CAS DataBase Reference: PHTHALIC ACID (RING-D4)(CAS DataBase Reference)
    12. NIST Chemistry Reference: PHTHALIC ACID (RING-D4)(87976-26-9)
    13. EPA Substance Registry System: PHTHALIC ACID (RING-D4)(87976-26-9)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 87976-26-9(Hazardous Substances Data)

87976-26-9 Usage

Uses

Used in Chemical Synthesis Industry:
Phthalic Acid (Ring-D4) is used as a key intermediate for the synthesis of phthalates, which are a class of esters derived from phthalic acid and alcohols. These phthalates are widely used as plasticizers, solvents, and in the production of various polymers and resins.
Used in Organic Reagent Industry:
Phthalic Acid (Ring-D4) is utilized as a labeled organic reagent in research and development, particularly in the synthesis of deuterated compounds. The deuterium labeling allows for enhanced analytical techniques and improved understanding of chemical reactions and processes.
Used in Plasticizer Production:
Phthalic Acid (Ring-D4) is used in the production of plasticizers, which are additives that increase the flexibility and workability of plastics. These plasticizers are commonly used in the manufacturing of vinyl products, such as pipes, films, and coatings.
Used in Solvent Production:
Phthalic Acid (Ring-D4) is also used in the production of solvents, which are liquids that dissolve other substances and are used in various industrial processes, such as cleaning, degreasing, and extraction.
Used in Polymer and Resin Production:
Phthalic Acid (Ring-D4) is employed in the synthesis of polymers and resins, which are high molecular weight compounds with a wide range of applications, including coatings, adhesives, and composite materials. These polymers and resins are used in various industries, such as automotive, construction, and electronics.

Check Digit Verification of cas no

The CAS Registry Mumber 87976-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,7 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87976-26:
(7*8)+(6*7)+(5*9)+(4*7)+(3*6)+(2*2)+(1*6)=199
199 % 10 = 9
So 87976-26-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4H,(H,9,10)(H,11,12)/i1D,2D,3D,4D

87976-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,5,6-tetradeuteriophthalic acid

1.2 Other means of identification

Product number -
Other names 3,4,5,6-tetradeuterio-phthalic 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:87976-26-9 SDS

87976-26-9Relevant articles and documents

An efficient and general method for the synthesis of stable isotope deuterium labeled phthalate esters

Xu, Zhongjie,Zhao, Cheng,Sun, Wen,Lei, Wen,Hu, Zuming

, p. 378 - 384 (2021/07/02)

An efficient and general synthetic route of deuterium-labeled phthalate esters is described with high isotopic enrichment and excellent chemical purities using inexpensive and readily available o-xylene-D10 as labeled starting material. The str

Efficient and selective Pt/C-catalyzed H-D exchange reaction of aromatic rings

Ito, Nobuhiro,Esaki, Hiroyoshi,Maesawa, Tsuneaki,Imamiya, Eikoh,Maegawa, Tomohiro,Sajiki, Hironao

experimental part, p. 278 - 286 (2009/03/12)

An effective and applicable deuteration method for aromatic rings using Pt/C-D2O-H2 system was established. Especially, phenol was fully deuterated even at room temperature, and other electron-rich aromatic nuclei were efficiently deuterated under mild conditions. The scope and limitations of the presence method and its application to the synthesis of deuterium-labeled biologically active compounds and deuterium-labeled building blocks for practical multi-gram scale syntheses are reported. 2008 The Chemical Society of Japan.

Aromatic ring favorable and efficient H-D exchange reaction catalyzed by Pt/C

Sajiki, Hironao,Ito, Nobuhiro,Esaki, Hiroyoshi,Maesawa, Tsuneaki,Maegawa, Tomohiro,Hirota, Kosaku

, p. 6995 - 6998 (2007/10/03)

An effective and applicable Pt/C-catalyzed deuteration method of aromatic rings using D2O as a deuterium source under hydrogen atmosphere was developed. Five percent Pt/C would lead to quite effective H-D exchange results on the aromatic ring systems. The reaction is general for a variety of aromatic compounds including biologically active compounds.

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