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2-Hydroxyethyl salicylate

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2-Hydroxyethyl salicylate Basic information

Product Name:
2-Hydroxyethyl salicylate
Synonyms:
  • SALICYLIC ACID ETHYLENE GLYCOL ESTER
  • 2-hydroxyethyl 2-hydroxybenzoate
  • Ethylene glycol Monosali
  • 1,2-Ethylene glycol monosalicylate
  • 2-Hydroxybenzoic acid 2-hydroxyethyl ester
  • 2-hydroxy-benzoicaci2-hydroxyethylester
  • Benzoic acid, 2-hydroxy-, 2-hydroxyethyl ester
  • beta-Hydroxyethyl salicylate
CAS:
87-28-5
MF:
C9H10O4
MW:
182.17
EINECS:
201-737-2
Product Categories:
  • Building Blocks
  • C8 to C9
  • Carbonyl Compounds
  • Chemical Synthesis
  • Esters
  • Organic Building Blocks
  • Heterocyclic Compounds
  • Ethylene Glycols & Monofunctional Ethylene Glycols
  • Monofunctional Ethylene Glycols
Mol File:
87-28-5.mol
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2-Hydroxyethyl salicylate Chemical Properties

Melting point:
25°C
Boiling point:
166 °C13 mm Hg(lit.)
Density 
1.244 g/mL at 25 °C(lit.)
vapor pressure 
0.0001 hPa (20 °C)
refractive index 
n20/D 1.548(lit.)
Flash point:
>230 °F
storage temp. 
Store below +30°C.
solubility 
13.1g/l
form 
Oily Liquid or Low Melting Solid
pka
8.00±0.30(Predicted)
Specific Gravity
1.244 (20/4℃)
color 
Colorless
PH
4.0 (13.1g/l, H2O, 20℃)
Merck 
14,4499
BRN 
2255685
InChIKey
LVYLCBNXHHHPSB-UHFFFAOYSA-N
LogP
1.519 (est)
CAS DataBase Reference
87-28-5(CAS DataBase Reference)
NIST Chemistry Reference
2-Hydroxyethyl salicylate(87-28-5)
EPA Substance Registry System
Benzoic acid, 2-hydroxy-, 2-hydroxyethyl ester (87-28-5)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
44
WGK Germany 
3
Autoignition Temperature
441 °C DIN 51794
HS Code 
2918 23 00
Toxicity
LD50 orally in Rabbit: 1380 mg/kg

MSDS

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2-Hydroxyethyl salicylate Usage And Synthesis

Chemical Properties

Colorless oily liquid or low melting solid

Uses

Glycol Salicylate, is a derivative of salicylic acid that has been proved to be able to improve the aesthetic appearance of the skin. It is also a building block used in various chemical synthesis.

Definition

ChEBI: A benzoate ester obtained by the formal condensation of carboxy group of salicylic acid with one of the hydroxy groups of ethylene glycol

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