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1,3-Benzenedicarboxylic acid, 5-(hydroxyMethyl)-, 1,3-diMethyl ester, also known as trimellitic acid tris-(3-methyl-1-oxopentyl) ester, is a chemical compound that serves as a plasticizer in the production of various plastics. It is a clear, colorless liquid that is insoluble in water but soluble in organic solvents. 1,3-Benzenedicarboxylic acid, 5-(hydroxyMethyl)-, 1,3-diMethyl ester is recognized for its ability to enhance the flexibility and durability of plastics, making them more versatile for a wide range of applications.

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  • 1,3-Benzenedicarboxylic acid, 5-(hydroxyMethyl)-, 1,3-dimethyl ester

    Cas No: 109862-53-5

  • USD $ 1.9-2.9 / Gram

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  • 1000 Metric Ton/Month

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  • 109862-53-5 Structure
  • Basic information

    1. Product Name: 1,3-Benzenedicarboxylic acid, 5-(hydroxyMethyl)-, 1,3-diMethyl ester
    2. Synonyms: 1,3-Benzenedicarboxylic acid, 5-(hydroxyMethyl)-, 1,3-diMethyl ester;diMethyl 5-(hydroxyMethyl)isophthalate;1,3-dimethyl 5-(hydroxymethyl)benzene-1,3-dicarboxylate
    3. CAS NO:109862-53-5
    4. Molecular Formula: C11H12O5
    5. Molecular Weight: 224.20998
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 109862-53-5.mol
  • Chemical Properties

    1. Melting Point: 106-107 °C
    2. Boiling Point: 376.0±37.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.252±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 14.23±0.10(Predicted)
    10. CAS DataBase Reference: 1,3-Benzenedicarboxylic acid, 5-(hydroxyMethyl)-, 1,3-diMethyl ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,3-Benzenedicarboxylic acid, 5-(hydroxyMethyl)-, 1,3-diMethyl ester(109862-53-5)
    12. EPA Substance Registry System: 1,3-Benzenedicarboxylic acid, 5-(hydroxyMethyl)-, 1,3-diMethyl ester(109862-53-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 109862-53-5(Hazardous Substances Data)

109862-53-5 Usage

Uses

Used in Plastics Industry:
1,3-Benzenedicarboxylic acid, 5-(hydroxyMethyl)-, 1,3-diMethyl ester is used as a plasticizer for improving the flexibility and durability of various plastics, such as polyvinyl chloride (PVC) and other polymers. Its incorporation into these materials results in enhanced physical properties, allowing for a broader spectrum of applications and uses.

Check Digit Verification of cas no

The CAS Registry Mumber 109862-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,8,6 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 109862-53:
(8*1)+(7*0)+(6*9)+(5*8)+(4*6)+(3*2)+(2*5)+(1*3)=145
145 % 10 = 5
So 109862-53-5 is a valid CAS Registry Number.

109862-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 5-(hydroxymethyl)benzene-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names dimethyl 5-hydroxymethylbenzene-1,3-dicarboxylate

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:109862-53-5 SDS

109862-53-5Relevant articles and documents

Hybrid materials based on novel 2D lanthanide coordination polymers covalently bonded to amine-modified SBA-15 and MCM-41: assembly, characterization, structural features, thermal and luminescence properties

Wang, Jun,Dou, Wei,Kirillov, Alexander M.,Liu, Weisheng,Xu, Cailing,Fang, Ran,Yang, Lizi

, p. 18610 - 18621 (2016)

Three novel 2D coordination polymers [Tb2(μ4-L)2(μ-HL)(μ-HCOO)(DEF)]n (Tb-L), [Eu(μ4-L)(L)(H2O)2]n (Eu-L), and [Nd(μ4-L)(L)(H2O)2]sub

A water-stable lanthanide coordination polymer as a multiresponsive luminescent sensor for Fe3+, Cr(vi) and 4-nitrophenol

Liu, Yan,Ma, Jingjing,Xu, Cong,Yang, Yang,Xia, Minfang,Jiang, Huie,Liu, Weisheng

, p. 13543 - 13549 (2018)

Constructing water stable lanthanide coordination polymers (Ln-CPs) is of great importance for practical applications in biological and environmental areas and necessary for systematic research on the relationship between the properties of Ln-CPs and stru

Rationally designed non-enzymatic fluorogenic 'turn-on' probe for uric acid

Pradhan, Tuhin,Maiti, Sukhendu,Kumar, Rajesh,Lee, Yun Hak,Kim, Jong Wan,Lee, Joung Hae,Kim, Jong Seung

, p. 1 - 6 (2015)

Abstract The simple and cost-effective detection of uric acid in serum or urine is highly desirable as uric acid acts as a biomarker for various diseases. Herein, we report a rationally designed, non-enzymatic probe for the detection of uric acid in serum samples over a wide range of concentrations (lower: ~60 μM, higher: ~700 μM and normal: ~120-380 μM) with 'turn-on' fluorogenic behaviour.

COMPOSITIONS AND METHODS RELATED TO MOLECULAR CONJUGATION

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Page/Page column 60; 61, (2021/06/11)

The invention relates to activated Michael acceptor (AMA) compounds that can undergo conjugation with biomolecules containing Michael donor moieties, thereby providing plasma-stable antibody-drug conjugates (ADCs). Pharmaceutical compositions of the ADCs are disclosed as well. Also provided herein are a number of applications (e.g., therapeutic applications) in which the compositions are useful.

Functional Porphyrinic Metal–Organic Framework as a New Class of Heterogeneous Halogen-Bond-Donor Catalyst

Chen, Yu-Sheng,Cheng, Qigan,Ma, Shengqian,Nafady, Ayman,Shan, Chuan,Wojtas, Lukasz,Zhang, Weijie,Zhang, X. Peter

supporting information, p. 24312 - 24317 (2021/10/04)

Biomimetic metal-organic frameworks have attracted great attention as they can be used as bio-inspired models, allowing us to gain important insights into how large biological molecules function as catalysts. In this work, we report the synthesis and utilization of such a metal-metalloporphyrin framework (MMPF) that is constructed from a custom-designed ligand as an efficient halogen bond donor catalyst for Diels–Alder reactions under ambient conditions. The implementation of fabricated halogen bonding capsule as binding pocket with high-density C?Br bonds enabled the use of halogen bonding to facilitate organic transformations in their three-dimensional cavities. Through combined experimental and computational studies, we showed that the substrate molecules diffuse through the pores of the MMPF, establishing a host-guest system via the C?Br???π interaction. The formation of halogen bonds is a plausible explanation for the observed boosted catalytic efficiency in Diels–Alder reactions. Moreover, the unique capability of MMPF highlights new opportunities in using artificial non-covalent binding pockets as highly tunable and selective catalytic materials.

BIVALENT TARGETED CONJUGATES

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Page/Page column 59; 60, (2020/05/28)

The invention provides conjugates that comprise a bivalent targeting moiety, a nucleic acid, and optional linking groups as well as synthetic intermediates and synthetic methods useful for preparing the conjugates, compositions comprising the bidentate targeting ligands and the conjugates, as well as methods for targeting therapeutic nucleic acids with the bidentate conjugates. The conjugates are useful to target therapeutic nucleic acids.

THERAPEUTIC METHODS

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Page/Page column 204; 231-232, (2020/05/28)

The invention provides methods and compositions for delivering a nucleic acid to a cell or the cytosol of the target cell. The method includes contacting the cell with, 1) a membrane-destabilizing polymer; and 2) a nucleic acid conjugate. The nucleic acid conjugate includes a targeting ligand bound to an optional linker and a nucleic acid.

Optimized reaction pair of the Cyshis tag and Ni(II)-Nta probe for highly selective chemical labeling of membrane proteins

Zenmyo, Naoki,Tokumaru, Hiroki,Uchinomiya, Shohei,Fuchida, Hirokazu,Tabata, Shigekazu,Hamachi, Itaru,Shigemoto, Ryuichi,Ojida, Akio

, p. 995 - 1000 (2019/07/18)

Chemical labeling of proteins with synthetic molecular probes offers the possibility to probe the functions of proteins of interest in living cells. However, the methods for covalently labeling targeted proteins using complementary peptide tag-probe pairs are still limited, irrespective of the versatility of such pairs in biological research. Herein, we report the new CysHis tag-Ni(II) probe pair for the specific covalent labeling of proteins. A broad-range evaluation of the reactivity profiles of the probe and the CysHis peptide tag afforded a tag-probe pair with an optimized and high labeling selectivity and reactivity. In particular, the labeling specificity of this pair was notably improved compared to the previously reported one. This pair was successfully utilized for the fluorescence imaging of membrane proteins on the surfaces of living cells, demonstrating its potential utility in biological research.

Radiolabeled Dibenzodiazepinone-Type Antagonists Give Evidence of Dualsteric Binding at the M2 Muscarinic Acetylcholine Receptor

Pegoli, Andrea,She, Xueke,Wifling, David,Hübner, Harald,Bernhardt, Günther,Gmeiner, Peter,Keller, Max

, p. 3314 - 3334 (2017/05/05)

The dualsteric ligand approach, aiming at ligands with improved subtype selectivity, has been increasingly applied to muscarinic receptors (MRs). In this article, we present the synthesis and characterization of a M2R subtype-preferring radiola

POTENT AND SELECTIVE INHIBITORS OF NAV1.7

-

, (2016/02/18)

Disclosed is a composition of matter comprising an isolated polypeptide, which is a peripherally-restricted NaV1.7 inhibitor. In some disclosed embodiments, the isolated polypeptide is an inhibitor of NaV1.7. Other embodiments are co

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