Welcome to LookChem.com Sign In|Join Free

CAS

  • or

87247-04-9

Post Buying Request

87247-04-9 Suppliers

Recommended suppliersmore

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

87247-04-9 Usage

Description

(3R,7R)-3,7,11-trimethyldodecan-1-ol is a chiral dodecanol, a type of fatty alcohol with a molecular formula of C15H32O. It is characterized by its three-dimensional structure with a chiral center, indicated by the (3R,7R) designation, and the presence of three methyl groups on the molecule. (3R,7R)-3,7,11-trimethyldodecan-1-ol is commonly found in natural fats and oils and is known for its unique chemical and physical properties.

Uses

Used in Fragrance Industry:
(3R,7R)-3,7,11-trimethyldodecan-1-ol is used as a fragrance ingredient for its pleasant odor, contributing to the creation of various scent profiles in perfumes, colognes, and other scented products.
Used in Pharmaceutical Industry:
(3R,7R)-3,7,11-trimethyldodecan-1-ol is used as a pharmaceutical excipient for its surfactant and emulsifying properties, aiding in the formulation and stabilization of medications.
Used in Cosmetic Industry:
In the cosmetic industry, (3R,7R)-3,7,11-trimethyldodecan-1-ol is used as a surfactant and emulsifier to improve the texture, consistency, and stability of cosmetic products, such as creams, lotions, and serums.
Used in Food Industry:
(3R,7R)-3,7,11-trimethyldodecan-1-ol is used as a flavoring agent and emulsifier in the food industry to enhance the taste and texture of various food products.

Check Digit Verification of cas no

The CAS Registry Mumber 87247-04-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,4 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87247-04:
(7*8)+(6*7)+(5*2)+(4*4)+(3*7)+(2*0)+(1*4)=149
149 % 10 = 9
So 87247-04-9 is a valid CAS Registry Number.

87247-04-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R*,7R*)-3,7,11-trimethyldodecan-1-ol

1.2 Other means of identification

Product number -
Other names (3R,7R)-3,7,11-Trimethyl-dodecan-1-ol

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:87247-04-9 SDS

87247-04-9Relevant articles and documents

Enantioselective Total Synthesis of the Archaeal Lipid Parallel GDGT-0 (Isocaldarchaeol)**

Falk, Isaac D.,Gál, Bálint,Bhattacharya, Ahanjit,Wei, Jeremy H.,Welander, Paula V.,Boxer, Steven G.,Burns, Noah Z.

supporting information, p. 17491 - 17496 (2021/06/15)

Archaeal glycerol dibiphytanyl glycerol tetraethers (GDGT) are some of the most unusual membrane lipids identified in nature. These amphiphiles are the major constituents of the membranes of numerous Archaea, some of which are extremophilic organisms. Due to their unique structures, there has been significant interest in studying both the biophysical properties and the biosynthesis of these molecules. However, these studies have thus far been hampered by limited access to chemically pure samples. Herein, we report a concise and stereoselective synthesis of the archaeal tetraether lipid parallel GDGT-0 and the synthesis and self-assembly of derivatives bearing different polar groups.

Tocopherol side chain synthesis via asymmetric organocatalytic transfer hydrogenation and convenient measurement of stereoselectivity

Lee, Hyunji,Lee, You-Kyoung,Kim, Dong-Guk,Son, Mi-Sun,Nam, Tae-Gyu,Jeong, Byeong-Seon

, p. 5895 - 5897 (2014/12/12)

An asymmetric synthetic route for 1-iodofarnesane, a key intermediate for tocopherol side chain synthesis, starting from (+)-(R)-citronellal was developed. 1-Iodofarnesane was prepared through eight steps in about 50% overall yield, and asymmetric transfe

ASYMMETRIC HYDROGENATION OF ALKENNES USING CHIRAL IRIDIUM COMPLEXES

-

Page/Page column 19, (2008/06/13)

The invention relates to the (stereoselective) hydrogenation of carbon-carbon double bonds in compounds having at least one such bond, e.g., isoprenoids, non-cyclic sesquiterpenes, tocomonoenols, tocodienols, tocotrienols or derivatives thereof, as well as to the (stereoselective) hydrogenation of parts/extracts of plant oils containing such tocotrienols or derivatives thereof, in the presence of a chiral Ir complex as the catalyst, whereby preferably one stereoisomer is manufactured in an excess.

Post a RFQ

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)

1

What can I do for you?
Get Best Price

Get Best Price for 87247-04-9