132796-57-7

• 

• Basic information

  1. Product Name: 3-hydroxysclareol
  2. Synonyms: 3-hydroxysclareol;(13R)-Labdan-14-ene-3β,8,13-triol
  3. CAS NO:132796-57-7
  4. Molecular Formula: C₂₀H₃₆O₃
  5. Molecular Weight: 324.49804
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 132796-57-7.mol
  9. Article Data: 5

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 434.3°Cat760mmHg
  3. Flash Point: 187.9°C
  4. Appearance: /
  5. Density: 1.013g/cm³
  6. Vapor Pressure: 2.29E-09mmHg at 25°C
  7. Refractive Index: 1.504
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 3-hydroxysclareol(CAS DataBase Reference)
  11. NIST Chemistry Reference: 3-hydroxysclareol(132796-57-7)
  12. EPA Substance Registry System: 3-hydroxysclareol(132796-57-7)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 132796-57-7(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

132796-57-7 Suppliers

Recommended suppliersmore

• Product
• FOB Price
• Min.Order
• Supply Ability
• Supplier
• Contact Supplier

• 3-HYDROXYSCLAREOL

  Cas No: 132796-57-7

• No Data

• No Data

• No Data

• Hangzhou Fandachem Co.,Ltd
• Contact Supplier

132796-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132796-57-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,7,9 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132796-57:
(8*1)+(7*3)+(6*2)+(5*7)+(4*9)+(3*6)+(2*5)+(1*7)=147
147 % 10 = 7
So 132796-57-7 is a valid CAS Registry Number.

InChI:InChI=1/C20H36O3/c1-7-18(4,22)11-8-15-19(5)12-10-16(21)17(2,3)14(19)9-13-20(15,6)23/h7,14-16,21-23H,1,8-13H2,2-6H3/t14-,15+,16-,18-,19-,20+/m0/s1

132796-57-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name	3β-hydroxysclareol

1.2 Other means of identification

Product number	-
Other names	labda-14-en-3β,8α,13β-triol

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:132796-57-7 SDS

132796-57-7Upstream product

• 515-03-7 sclareol 
• 117015-26-6 8α,13β-dihydroxylabd-14-en-3-one 

132796-57-7Downstream Products

132796-57-7Relevant articles and documents

Microbial hydroxylation of sclareol by Rhizopus stolonifer

Diez,Sanchez,Rodilla,Rocha,Mendes,Paulino,Marcos,Basabe,Urones

, p. 1005 - 1009 (2005)

Incubation of sclareol with Rhizopus stolonifer affords in high yield a mixture of triols with 18-hydroxy-sclareol as the main component.

Characterization of the antifungal activity against botrytis cinerea of sclareol and 13-epi-sclareol, two labdane-type diterpenoids

Mendoza, Leonora,Sepúlveda, Carolina,Melo, Ricardo,Cotoras, Milena

, p. 3024 - 3028 (2015)

The antifungal activity of Sclareol and 13-epi-Sclareol, two labdane-type diterpenoids, on mycelial growth of the phytopathogenic fungus Botrytis cinerea was evaluated. Diterpenoid fungitoxicity was assessed using the radial growth test method. Both diterpenoids inhibited the mycelial growth of B. cinerea in solid medium; however the inhibitory activity of Sclareol was slightly higher than 13-epi-Sclareol with IC50 value of 237.6 μg/mL and 268.8 μg/mL, respectively. On the other hand, both labdane-type diterpenoids did not alter the plasmatic membrane integrity; however the oxygen consumption of B. cinerea germinating conidia was affected. The evidence suggests that action mechanism of these molecules would be related to the uncoupling of mitochondrial oxidative phosphorylation. Finally, biotransformation of Sclareol by B. cinerea was analysed and the main biotransformed metabolite was identified as 3β-hydroxysclareol.

Microbial metabolism of the diterpene sclareol: Oxidation of the A ring by Septomyxa affinis

Kouzi,McChesney

, p. 2157 - 2164 (2007/10/02)

-

Post a RFQ

Cas No.:

Product Name:

Quantity:

Please select Metric Ton KG G Pound L ML

Email:

Company name:

Valid Period:

Detailed Requirements:

• Sample
• MOQ
• GMP
• FDA
• Price
• Urgent purchase

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

Remove

Submit

1

What can I do for you?
Get Best Price

Get Best Price for 132796-57-7 3-hydroxysclareol

Send

Send

Metric Ton KG G Pound L ML

Send

Send