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

Austria 1 China 7 Europe 3 Japan 1 United Kingdom 1 United States 1 Global 14

U-Chemo Scientific(Shanghai) Co.,Ltd

Tel: 021-58380326 13585932672
Email: 3251669772@qq.com
Country: China
ProdList: 534
Advantage: 58

TCI (Shanghai) Chemical Trading Co., Ltd.

Tel: 021-021-61109150
Fax: 021-61105897
Email: sales@tcisct.com
Country: China
ProdList: 31121
Advantage: 58

Shaanxi DIDU pharmaceutical and Chemical Co., Ltd

Tel: 15229059051
Email: 1027@dideu.com
Country: China
ProdList: 9989
Advantage: 58

Jiangsu Aikon Biopharmaceutical R&D Co.,Ltd.

Tel: 025-66061636 18013972705
Email: qqyang@aikonchem.com
Country: China
ProdList: 10238
Advantage: 58

Shaanxi Didu New Materials Co. Ltd

Tel: +86-89586680 +86-13289823923
Email: 1026@dideu.com
Country: China
ProdList: 8670
Advantage: 58

498-71-5, SOBREROLRelated Search:

3-Cyclohexene-1-methanol (-)-cis-Sobrerol d,l-trans-Sobrerol,dl-Sobrerol,dl-trans-sobrero DL-trans-sobrerol theophylline-7-acetate,Sobrerol theophyllineacetate TRANS-SOBREROL

1-P-MENTHENE-6,8-DIOL

AURORA KA-476

SOBREROL

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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

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498-71-5

C10H16OH2