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SOBREROL

Product Name
SOBREROL
CAS No.
498-71-5
Chemical Name
SOBREROL
Synonyms
Soberol;SOBREROL;Pinol hydrate;AURORA KA-476;1-METHANE-6,8-DIOL;1-P-MENTHENE-6,8-DIOL;p-Menth-1-ene-6,8-diol;p-menth-6-ene-2,8-diol;5-Hydroxy-α,α,4-trimethyl-3-cyclohexene-1-methanol;α,α,4-Trimethyl-5-hydroxy-3-cyclohexene-1-methanol
CBNumber
CB9341175
Molecular Formula
C10H18O2
Formula Weight
170.25
MOL File
498-71-5.mol
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SOBREROL Property

Melting point:
130°C
Boiling point:
259.9°C (rough estimate)
Density 
0.9581 (rough estimate)
refractive index 
1.5130 (estimate)
pka
14.69±0.60(Predicted)
Water Solubility 
32g/L(15 ºC)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0004191
Product name
SOBEROL
Purity
95.00%
Packaging
1G
Price
$179.55
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0004191
Product name
SOBEROL
Purity
95.00%
Packaging
500G
Price
$4467.77
Updated
2021/12/16
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SOBREROL Chemical Properties,Usage,Production

Chemical Properties

White or colorless crystals. M.P. 148℃. Insoluble in water, soluble in alcohol and oils.

Originator

Sobrepin,Corvi,Italy,1970

Uses

Pinol hydrate could find use in detergent perfumes, fragrances for household products, etc.

Preparation

Pinol hydrate is produced by hydrolytic autoxidation of alpha-pinene. It is also formed by heating of Pinol, or by treatment of Pinene with Lead tetra-acetate.

Definition

ChEBI: Sobrerol is a p-menthane monoterpenoid.

Manufacturing Process

To 19 l of well-agitated distilled water plus 18 g of ditertiary-butyl-p-cresol was added 19.84 kg (130 mols) of pure α-pinene oxide that was about half racemic, half d-form. The temperature was maintained at 30°C to 50°C, first with ice bath cooling and then with tap water cooling. The addition of the pinene oxide required 1,5 hours. After the addition was complete and the exothermic reaction was about over, the mixture was stirred for 2,5 hours at about 30°C, and then centrifuged to separate the crude sobrerol from the liquid phase consisting of oil and water.
The crude sobrerol was washed with naphtha and then air dried to yield 14.81 kg (87.5 mols) of pure sobrerol, [α]D 25 -77.0°. It was found that 1 liter of the aqueous phase from the reaction contained 22 g of sobrerol, so, therefore, the entire aqueous phase contained 0.42 kg (2.5 mols) of sobrerol.

Therapeutic Function

Mucolytic

SOBREROL Preparation Products And Raw materials

Raw materials

Preparation Products

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SOBREROL Suppliers

ecochem international chemical broker
Tel
--
Fax
--
Email
export@ecochem.dk
Country
Europe
ProdList
6371
Advantage
66
kemikalieimport
Tel
--
Fax
--
Email
Sales@kemikalieimport.dk
Country
Europe
ProdList
6685
Advantage
47
Camida
Tel
--
Fax
--
Email
info@camida.com
Country
Europe
ProdList
3704
Advantage
71

498-71-5, SOBREROLRelated Search:


  • 1-P-MENTHENE-6,8-DIOL
  • AURORA KA-476
  • SOBREROL
  • 5-hydroxy-alpha,alpha,4-trimethylcyclohex-3-ene-1-methanol
  • 5-Hydroxy-α,α,4-trimethyl-3-cyclohexene-1-methanol
  • Pinol hydrate
  • 1-METHANE-6,8-DIOL
  • 2-Methyl-5-(1-methyl-1-hydroxyethyl)-2-cyclohexene-1-ol
  • p-Menth-1-ene-6,8-diol
  • α,α,4-Trimethyl-5-hydroxy-3-cyclohexene-1-methanol
  • p-menth-6-ene-2,8-diol
  • 5-(1-hydroxy-1-methyl-ethyl)-2-methyl-cyclohex-2-en-1-ol
  • Soberol
  • 5-(2-hydroxypropan-2-yl)-2-methyl-cyclohex-2-en-1-ol
  • 5-(2-hydroxypropan-2-yl)-2-methylcyclohex-2-en-1-ol
  • 3-Cyclohexene-1-methanol, 5-hydroxy-α,α,4-trimethyl-
  • 498-71-5
  • C10H16OH2