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3-Hydroxy-5-Methylbenzaldehyde is an aromatic organic compound characterized by its chemical formula C8H8O2. It is known for its white to light yellow appearance and possesses a pleasant, sweet, aromatic scent. 3-Hydroxy-5-Methylbenzaldehyde is widely recognized for its applications in the creation of various fragrances and flavors.

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  • 60549-26-0 Structure
  • Basic information

    1. Product Name: 3-Hydroxy-5-Methylbenzaldehyde
    2. Synonyms: 3-Hydroxy-5-Methylbenzaldehyde
    3. CAS NO:60549-26-0
    4. Molecular Formula: C8H8O2
    5. Molecular Weight: 136.14792
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 60549-26-0.mol
  • Chemical Properties

    1. Melting Point: 107-108 °C(Solv: chloroform (67-66-3))
    2. Boiling Point: 259.2±20.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.175±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. PKA: 9.35±0.10(Predicted)
    10. CAS DataBase Reference: 3-Hydroxy-5-Methylbenzaldehyde(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Hydroxy-5-Methylbenzaldehyde(60549-26-0)
    12. EPA Substance Registry System: 3-Hydroxy-5-Methylbenzaldehyde(60549-26-0)
  • 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: 60549-26-0(Hazardous Substances Data)

60549-26-0 Usage

Uses

Used in Flavor and Fragrance Industry:
3-Hydroxy-5-Methylbenzaldehyde is used as a flavoring agent for imparting distinctive vanilla and almond flavors to food products. Its unique aromatic properties make it a valuable ingredient in the food industry, enhancing the taste and aroma of a variety of dishes and confectioneries.
Used in Perfumery:
In the perfume industry, 3-Hydroxy-5-Methylbenzaldehyde is utilized as a fixative and scent component. Its sweet, aromatic scent contributes to the longevity and complexity of perfumes, making it an essential component in creating long-lasting and appealing fragrances.
Used in Pharmaceutical Synthesis:
3-Hydroxy-5-Methylbenzaldehyde serves as a crucial intermediate in the synthesis of various pharmaceutical compounds. Its chemical properties allow it to be a key building block in the development of new drugs, playing a significant role in the advancement of medicinal chemistry.
Used in Chemical Industry:
As an important intermediate in the chemical industry, 3-Hydroxy-5-Methylbenzaldehyde is involved in the production of a range of chemical products. Its versatility in chemical reactions makes it a valuable component in the synthesis of various compounds used across different sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 60549-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,4 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60549-26:
(7*6)+(6*0)+(5*5)+(4*4)+(3*9)+(2*2)+(1*6)=120
120 % 10 = 0
So 60549-26-0 is a valid CAS Registry Number.

60549-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Hydroxy-5-methylbenzaldehyde

1.2 Other means of identification

Product number -
Other names -

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:60549-26-0 SDS

60549-26-0Relevant articles and documents

NOVEL METAL FREE PROCESS FOR ALLYLIC OXIDATION

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Page/Page column 10, (2015/02/25)

The patent discloses a novel metal free process for the preparation of corresponding phenol and ketone via allylic oxidation of substituted cyclohexenes. Air is used as oxidant in the present process and can be used as such or optionally selected from pure oxygen or atmospheric oxygen. Moreover, the process of the present invention utilizes easily available starting materials and is a green eco-friendly, convenient and economical process with high yield of >60 % and high selectivity

Roles of the synergistic reductive O-methyltransferase GilM and of O-methyltransferase GilMT in the gilvocarcin biosynthetic pathway

Tibrewal, Nidhi,Downey, Theresa E.,Van Lanen, Steven G.,Ul Sharif, Ehesan,O'Doherty, George A.,Rohr, Juergen

, p. 12402 - 12405 (2012/09/05)

Two enzymes of the gilvocarcin biosynthetic pathway, GilMT and GilM, with unclear functions were investigated by in vitro studies using purified, recombinant enzymes along with synthetically prepared intermediates. The studies revealed GilMT as a typical

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