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3-Carboxy-4-hydroxy-5-methoxybenzaldehyde is an organic compound with the molecular formula C8H8O5. It is a derivative of benzaldehyde, featuring a carboxylic acid, hydroxyl, and methoxy group at the 3rd, 4th, and 5th positions, respectively. 3-CARBOXY-4-HYDROXY-5-METHOXYBENZALDEHYDE is known for its potential applications in various industries due to its unique chemical structure and properties.

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  • 3507-08-2 Structure
  • Basic information

    1. Product Name: 3-CARBOXY-4-HYDROXY-5-METHOXYBENZALDEHYDE
    2. Synonyms: 5-Formyl-2-hydroxy-3-methoxybenzoic acid;2-hydroxy-5-methanoyl-3-methoxy-benzoic acid;3-CARBOXY-4-HYDROXY-5-METHOXYBENZALDEHYDE;5-CARBOXYVANILLIN;5-formyl-3-methoxysalicylic acid
    3. CAS NO:3507-08-2
    4. Molecular Formula: C9H8O5
    5. Molecular Weight: 196.16
    6. EINECS: 222-504-1
    7. Product Categories: Aromatic Aldehydes & Derivatives (substituted)
    8. Mol File: 3507-08-2.mol
  • Chemical Properties

    1. Melting Point: 272 °C
    2. Boiling Point: 386.9°Cat760mmHg
    3. Flash Point: 159.7°C
    4. Appearance: /
    5. Density: 1.441g/cm3
    6. Vapor Pressure: 1.11E-06mmHg at 25°C
    7. Refractive Index: 1.631
    8. Storage Temp.: -20°C Freezer, Under inert atmosphere
    9. Solubility: DMSO (Slightly), Methanol (Slightly, Sonicated)
    10. PKA: 2.44±0.14(Predicted)
    11. CAS DataBase Reference: 3-CARBOXY-4-HYDROXY-5-METHOXYBENZALDEHYDE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 3-CARBOXY-4-HYDROXY-5-METHOXYBENZALDEHYDE(3507-08-2)
    13. EPA Substance Registry System: 3-CARBOXY-4-HYDROXY-5-METHOXYBENZALDEHYDE(3507-08-2)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22-36
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 3507-08-2(Hazardous Substances Data)

3507-08-2 Usage

Uses

Used in Detergent Industry:
3-Carboxy-4-hydroxy-5-methoxybenzaldehyde is used as a bluing agent precursor in the detergent industry for unit dose detergents. Its application reason is to enhance the whiteness and brightness of fabrics during the washing process by providing a blue tint that counteracts the yellowing that can occur in fabrics over time.

Check Digit Verification of cas no

The CAS Registry Mumber 3507-08-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,0 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3507-08:
(6*3)+(5*5)+(4*0)+(3*7)+(2*0)+(1*8)=72
72 % 10 = 2
So 3507-08-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O5/c1-14-7-3-5(4-10)2-6(8(7)11)9(12)13/h2-4,11H,1H3,(H,12,13)

3507-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-formyl-2-hydroxy-3-methoxybenzoic acid

1.2 Other means of identification

Product number -
Other names 5-Carboxyvanillin

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:3507-08-2 SDS

3507-08-2Relevant articles and documents

Regioselective Enzymatic Carboxylation of Bioactive (Poly)phenols

Plasch, Katharina,Resch, Verena,Hitce, Julien,Pop?oński, Jaros?aw,Faber, Kurt,Glueck, Silvia M.

, p. 959 - 965 (2017/03/27)

In order to extend the applicability of the regioselective enzymatic carboxylation of phenols, the substrate scope of o-benzoic acid (de)carboxylases has been investigated towards complex molecules with an emphasis on flavouring agents and polyphenols possessing antioxidant properties. o-Hydroxycarboxylic acid products were obtained with perfect regioselectivity, in moderate to excellent yields. The applicability of this method was proven by the regioselective bio-carboxylation of resveratrol on a preparative scale with 95% yield. (Figure presented.).

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