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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
Molecular Weight:
170.25
MDL Number:
MFCD00009965
MOL File:
498-71-5.mol
Last updated:2023-05-04 17:34:39

SOBREROL Properties

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)
FDA UNII AI0NX02O35
ATC code R05CB07

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338

SOBREROL price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0004191 SOBEROL 95.00% 498-71-5 1G $179.55 2021-12-16 Buy
American Custom Chemicals Corporation API0004191 SOBEROL 95.00% 498-71-5 500G $4467.77 2021-12-16 Buy
Product number Packaging Price Buy
API0004191 1G $179.55 Buy
API0004191 500G $4467.77 Buy

SOBREROL Chemical Properties,Uses,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

SOBREROL Suppliers

Global( 14)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923 1026@dideu.com China 8670 58
U-Chemo Scientific(Shanghai) Co.,Ltd 021-58380326 13585932672 3251669772@qq.com China 534 58
TCI (Shanghai) Chemical Trading Co., Ltd. 021-021-61109150 sales@tcisct.com China 31121 58
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd 15229059051 1027@dideu.com China 9989 58
Jiangsu Aikon Biopharmaceutical R&D Co.,Ltd. 025-66061636 18013972705 qqyang@aikonchem.com China 10238 58
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 5-(2-hydroxypropan-2-yl)-2-methyl-cyclohex-2-en-1-ol 5-(2-hydroxypropan-2-yl)-2-methylcyclohex-2-en-1-ol Soberol 3-Cyclohexene-1-methanol, 5-hydroxy-α,α,4-trimethyl- 498-71-5 C10H16OH2