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ChemicalBook > Product Catalogue >Chemical Reagents >Organic reagents >Aromatic acids >3-(3-METHYLPHENYL)PROPIONIC ACID

3-(3-METHYLPHENYL)PROPIONIC ACID

3-(3-METHYLPHENYL)PROPIONIC ACID Structure
  • ₹0
  • Product name: 3-(3-METHYLPHENYL)PROPIONIC ACID
  • CAS: 3751-48-2
  • MF: C10H12O2
  • MW: 164.2
  • EINECS:
  • MDL Number:MFCD00060326
  • Synonyms:3-m-Tolylpropionic acid;HydrocinnaMic acid, M-Methyl-;3-(3-Methylphenyl)propionic acid, 96%, 96%;m-Methylhydrocinnamic acid;3-METHYLHYDROCINNAMIC ACID;3-(3-METHYLPHENYL)PROPANOIC ACID;3-(3-METHYLPHENYL)PROPIONIC ACID;Propionic acid, 3-[3-methylphenyl]-
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Melting point :39-42 °C (lit.)
Boiling point :290℃
Density :1.097
Flash point :>230 °F
storage temp. :Sealed in dry,Room Temperature
solubility :Acetone, DMSO, Methanol
form :Solid
pka :pK1:4.677 (25°C)
color :Off-White to Pale Yellow
CAS DataBase Reference :3751-48-2(CAS DataBase Reference)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 May cause respiratory irritation Specific target organ toxicity, single exposure;Respiratory tract irritation Category 3 Warning GHS hazard pictograms
Precautionary statements:
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P304+P340 IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405 Store locked up.

Description

3-m-Tolylpropanoic Acid is used in the synthesis of piperidine antagonists as CCR1-selective inhibitors. via parallel synthesis. Also used in the synthesis of small molecule antagonists of vasoactive intestinal. peptide receptor1 (VIPR1).

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