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CAS RN: 90-05-1 | Product Number: M0121

Guaiacol


Purity: >98.0%(GC)
Synonyms:
  • Catechol Monomethyl Ether
  • 2-Hydroxyanisole
  • 2-Methoxyphenol
  • Pyrocatechol Monomethyl Ether
Documents:
25G
£14.00
8   ≥20 
500G
£33.00
2   ≥20 

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Product Number M0121
Purity / Analysis Method >98.0%(GC)
Molecular Formula / Molecular Weight C__7H__8O__2 = 124.14  
Physical State (20 deg.C) Solid
Store Under Inert Gas Store under inert gas
Condition to Avoid Light Sensitive,Air Sensitive
CAS RN 90-05-1
Reaxys Registry Number 508112
PubChem Substance ID 87572226
SDBS (AIST Spectral DB) 1942
Merck Index (14) 4553
MDL Number

MFCD00002185

Specifications
Appearance White or Colorless to Light yellow powder to lump to clear liquid
Purity(GC) min. 98.0 %
Solubility in Methanol almost transparency
Properties (reference)
Melting Point 28 °C
Boiling Point 205 °C
Refractive Index 1.54
Solubility in water Slightly soluble
Solubility (very soluble in) Toluene,Benzene,Alcohol,Chloroform,Ether
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H302 + H332 : Harmful if swallowed or if inhaled.
H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
H336 : May cause drowsiness or dizziness.
H412 : Harmful to aquatic life with long lasting effects.
Precautionary Statements P261 : Avoid breathing dust/ fume/ gas/ mist/ vapours/ spray.
P273 : Avoid release to the environment.
P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ eye protection/ face protection.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P304 + P340 + P312 : IF INHALED: Remove person to fresh air and keep comfortable for breathing. Call a POISON CENTER/doctor if you feel unwell.
Related Laws:
EC Number 201-964-7
RTECS# SL7525000
Transport Information:
HS Number 2909500090
Application
Guaiacol: A Phenolic Natural Product Used as an Antiseptic Agent and a Synthetic Precursor

Guaiacol is a phenolic natural product first isolated from Guaiacum sp. It is also found in essential oils from celery seeds, tobacco leaves, orange leaves, and lemon peels. It tends to undergo autoxidation in the presence of molecular oxygen and light. It is commonly used as an antiseptic agent, and a synthetic precursor of various flavorants, such as vanillin and eugenol.

References


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