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3,6,9,12-Tetraoxapentacosan-1-ol, commonly known as triacontanol, is a long-chain primary alcohol with a 30-carbon backbone and four oxygen atoms in its structure. It is a fatty alcohol found in plant waxes and cuticles, known for its plant growth-promoting properties. Triacontanol has a high melting point and emulsifying properties, making it a versatile compound with potential applications in various industries.

930-08-5

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930-08-5 Usage

Uses

Used in Agriculture:
3,6,9,12-Tetraoxapentacosan-1-ol is used as a plant growth promoter for enhancing the yield and quality of crops. When applied in small concentrations, it has been shown to improve plant growth and development.
Used in Pharmaceutical Industry:
3,6,9,12-Tetraoxapentacosan-1-ol is used as an ingredient in pharmaceutical formulations due to its high melting point and emulsifying properties. These characteristics make it suitable for the development of various drug delivery systems and formulations.
Used in Cosmetic Industry:
In the cosmetic industry, 3,6,9,12-Tetraoxapentacosan-1-ol is used as an emulsifier and thickening agent. Its emulsifying properties allow it to blend oil and water-based ingredients, creating stable formulations for various cosmetic products.
Used in Biofuel Industry:
3,6,9,12-Tetraoxapentacosan-1-ol has been investigated for its potential as a biofuel. Its long-chain structure and alcohol functionality make it a candidate for conversion into biofuels, offering a renewable and sustainable energy source.
Used in Organic Synthesis:
3,6,9,12-Tetraoxapentacosan-1-ol serves as a precursor for the synthesis of other organic compounds. Its unique structure and functional groups can be utilized in various chemical reactions to produce a range of valuable organic molecules for different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 930-08-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 930-08:
(5*9)+(4*3)+(3*0)+(2*0)+(1*8)=65
65 % 10 = 5
So 930-08-5 is a valid CAS Registry Number.
InChI:InChI=1/C21H44O5/c1-2-3-4-5-6-7-8-9-10-11-12-14-23-16-18-25-20-21-26-19-17-24-15-13-22/h22H,2-21H2,1H3

930-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-[2-(2-tridecoxyethoxy)ethoxy]ethoxy]ethanol

1.2 Other means of identification

Product number -
Other names 3,6,9,12-Tetraoxapentacosan-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:930-08-5 SDS

930-08-5Upstream product

930-08-5Downstream Products

930-08-5Relevant academic research and scientific papers

Combinatorial synthesis of PEG oligomer libraries

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Page/Page column 9, (2010/02/15)

A simple chain-extending approach was established for the scale-up of the monoprotected monodisperse PEG diol materials. Reactions of THP-(OCH2CH2)n—OMs (n=4, 8, 12) with a large excess of commercially available H—(OCH2CH2)n—OH (n=1-4) under basic conditions led to THP-(OCH2CH2)n—OH (n=5-15). Similarly, Me-(OCH2CH2)n—OH (n=4-11, 13) were prepared from Me-(OCH2CH2)n—OMs (n=3, 7, 11). For the chain elongation steps, 40-80% yields were achieved through extraction purification. PEG oligomer libraries I and II were generated in 50-95% overall yields by alkylation or acylation of THP-(OCH2CH2)n—OH (n=1-15) followed by deprotection. Alkylation of Me-(OCH2CH2)n—OH (n=1-11, 13) with X—(CH2)m—CO2R (X=Br or OMs) and subsequent hydrolysis led to PEG oligomer library III in 30-60% overall yields. Combinatorial purification techniques were adapted to the larger-scale library synthesis. A total of 498 compounds, each with a weight of 2-5 g and a minimum purity of 90%, were synthesized.

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