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  • 3328-70-9 Structure
  • Basic information

    1. Product Name: 4-HYDROXYISOPHTHALALDEHYDE
    2. Synonyms: BUTTPARK 85\50-29;2,4-DIFORMYLPHENOL;4-HYDROXYISOPHTHALALDEHYDE;5-FORMYL-2-HYDROXYBENZALDEHYDE;5-FORMYLSALICYLALDEHYDE;TIMTEC-BB SBB004073;4-HYDROXYISOPHTHALALDEHYDE 98+%;4-Hydroxyisophthaladehyde
    3. CAS NO:3328-70-9
    4. Molecular Formula: C8H6O3
    5. Molecular Weight: 150.13
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3328-70-9.mol
    9. Article Data: 29
  • Chemical Properties

    1. Melting Point: 109°C
    2. Boiling Point: 266 °C at 760mmHg
    3. Flash Point: 128.9 °C
    4. Appearance: /
    5. Density: 1.35 g/cm3
    6. Vapor Pressure: 0.00538mmHg at 25°C
    7. Refractive Index: 1.672
    8. Storage Temp.: 2-8°C
    9. Solubility: soluble in Methanol
    10. PKA: 5.98±0.18(Predicted)
    11. CAS DataBase Reference: 4-HYDROXYISOPHTHALALDEHYDE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-HYDROXYISOPHTHALALDEHYDE(3328-70-9)
    13. EPA Substance Registry System: 4-HYDROXYISOPHTHALALDEHYDE(3328-70-9)
  • 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: 3328-70-9(Hazardous Substances Data)

3328-70-9 Usage

Description

4-Hydroxyisophthalaldehyde (4-HIPA) is a versatile aldehyde compound characterized by the presence of a hydroxyl group at the 4 position on its aromatic ring. It is renowned for its reactivity and serves as a crucial starting material in the synthesis of a variety of pharmaceuticals, agrochemicals, and organic compounds. The unique structure of 4-HIPA allows it to participate in multiple chemical reactions, including condensation, oxidation, and reduction, leading to the formation of a broad spectrum of functionalized derivatives. Its value in the chemical industry is further enhanced by its potential role in the development of new materials and its application in catalysis.

Uses

Used in Pharmaceutical Industry:
4-Hydroxyisophthalaldehyde is used as a key intermediate for the synthesis of various pharmaceuticals, leveraging its reactivity to form complex organic molecules that possess therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 4-HIPA is utilized as a starting material for the production of compounds that contribute to crop protection and enhancement of agricultural yields.
Used in Organic Compounds Synthesis:
4-Hydroxyisophthalaldehyde serves as a building block in the synthesis of diverse organic compounds, capitalizing on its ability to undergo a range of chemical reactions to create functionalized derivatives.
Used in Material Development:
4-HIPA is employed in the development of new materials, taking advantage of its unique chemical properties to engineer innovative substances with specialized applications.
Used in Catalysis:
As a component in catalytic processes, 4-Hydroxyisophthalaldehyde contributes to the efficiency and selectivity of chemical reactions, further expanding its utility in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 3328-70-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3328-70:
(6*3)+(5*3)+(4*2)+(3*8)+(2*7)+(1*0)=79
79 % 10 = 9
So 3328-70-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O3/c9-4-6-1-2-8(11)7(3-6)5-10/h1-5,11H

3328-70-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxybenzene-1,3-dicarbaldehyde

1.2 Other means of identification

Product number -
Other names 3-formyl-4-hydroxybenzaldehyde

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:3328-70-9 SDS

3328-70-9Relevant articles and documents

A nitroreductase and glutathione responsive nanoplatform for integration of gene delivery and near-infrared fluorescence imaging

Barz, Matthias,Bi, Qunjie,Chen, Xiaobing,Hu, Ao,Jin, Rongrong,Ke, Bowen,Liang, Hong,Nie, Yu,Song, Xu

, p. 6949 - 6952 (2020)

A novel platform rationally integrating indocyanine green analogues and an arginine-rich dendritic peptide with both nitroreductase (NTR) and glutathione (GSH) reduction responsive linkers was developed. This multifunctional platform can enable selective

Fluorescent probe for fluorine ion detection, application of fluorescent probe and method for detecting fluorine ions in to-be-detected sample

-

Paragraph 0047; 0051; 0056-0057, (2021/08/06)

The invention belongs to the technical field of analytical chemistry, and particularly relates to a fluorescent probe for fluorine ion detection, application of the fluorescent probe and a method for detecting fluorine ions in a to-be-detected sample. The invention provides a compound as shown in a formula I, or an optical isomer or salt thereof, and provides application of the compound as a fluorine ion detection fluorescent probe. According to the method for detecting the fluorine ions in the to-be-detected sample, the compound, or the optical isomer or the salt of the compound is used as a fluorine ion detection fluorescent probe for detection. The fluorescent probe has the advantages of good water solubility, high selectivity, high response speed, low detection limit, good stability, wide applicable pH range and good application prospect.

Cyanine fluorescent probe as well as preparation method and application thereof

-

Paragraph 0114-0118, (2021/09/04)

The invention discloses a cyanine fluorescent probe as well as a preparation method and application thereof. The fluorescent probe has a structure as shown in a structural general formula I, a one Doner-two Accepter structure is formed on a methine chain

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