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3-Butyl-1-heptanol, also known as 3-n-butylheptanol, is an organic compound belonging to the alcohol family. It is a colorless liquid with a distinctive odor and is characterized by its long hydrocarbon chain and a butyl group attached to the third carbon. This unique structure endows 3-butyl-1-heptanol with specific properties that make it suitable for various applications across different industries.

51655-56-2

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51655-56-2 Usage

Uses

Used in Chemical Synthesis:
3-Butyl-1-heptanol is used as a reagent in the preparation of branched acyl alkyl fluorens, which form a smectic A phase. This application is particularly relevant in the field of material science, where the smectic A phase is a liquid crystalline phase with potential uses in display technologies and other advanced materials.
Used in Fragrance Industry:
Due to its distinctive odor, 3-butyl-1-heptanol can be used as a fragrance ingredient in the perfumery and cosmetics industry. Its unique scent profile can contribute to the creation of various fragrances and scents for personal care products.
Used in Flavor Industry:
3-Butyl-1-heptanol may also find application in the flavor industry, where it can be used to enhance or modify the taste of various food and beverage products. Its ability to impart a specific flavor note can be valuable in the development of new and innovative flavors.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-butyl-1-heptanol could potentially be utilized as a solvent or intermediate in the synthesis of various drugs and active pharmaceutical ingredients. Its chemical properties make it a versatile compound for use in the development of new medications.
Used in Research and Development:
3-Butyl-1-heptanol may also be employed in research and development settings, where it can be used as a model compound to study the properties and behavior of long-chain alcohols and their derivatives. This can contribute to the advancement of scientific knowledge and the development of new materials and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 51655-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,5 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51655-56:
(7*5)+(6*1)+(5*6)+(4*5)+(3*5)+(2*5)+(1*6)=122
122 % 10 = 2
So 51655-56-2 is a valid CAS Registry Number.

51655-56-2SDS

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 3-butylheptan-1-ol

1.2 Other means of identification

Product number -
Other names 3-BUTYL-1-HEPTANOL

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:51655-56-2 SDS

51655-56-2Relevant articles and documents

BRANCHED TAIL LIPID COMPOUNDS AND COMPOSITIONS FOR INTRACELLULAR DELIVERY OF THERAPEUTIC AGENTS

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Paragraph 00335; 00357, (2021/04/01)

The application relates to lipids of Formula (A), Formula (B) and Formula (1-1), and to lipid nanoparticles (empty or loaded LNPs) including such a lipid as well as additional lipids such as phospholipids, structural lipids, and PEG lipids. Lipid nanoparticles further including therapeutic and/or prophylactics such as RNA are useful in the delivery of therapeutic and/or prophylactics to mammalian cells or organs to, for example, regulate polypeptide, protein, or gene expression.

LNP COMPOSITIONS COMPRISING MRNA THERAPEUTICS WITH EXTENDED HALF-LIFE

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Page/Page column 306; 0307; 308, (2022/01/04)

The disclosure features a polynucleotide encoding a polypeptide, which polynucleotide comprises: a 5'UTR described herein; a coding region comprising a payload and a stop element described herein; and a 3'UTR described herein, and LNP compositions comprising the same. The polynucleotides and/or LNP compositions of the present disclosure can: increase the level and/or activity of the payload by increasing the half-life and/or duration of expression of the polynucleotide encoding the payload or of the payload polypeptide. Also disclosed herein are methods of treating a disease or disorder in a subject using the LNP compositions of the present disclosure.

Synthetic method for gamma-dialkyl bromopropane

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Paragraph 0018, (2018/06/15)

The invention discloses a synthetic method for gamma-dialkyl bromopropane. The method is characterized by comprising the following steps: step 1, in the presence of an alkali, a compound I and triethyl phosphonoacetate are subjected to a Horner-Wadsworth-Emmons reaction to form a compound II; step 2, the compound II and palladium on carbon are subjected to a hydrogenation reduction reaction to form a compound III; step 3, the compound III is subjected to a reduction reaction under the action of NaBH4 to form a compound IV; and step 4, the compound IV and a bromide are subjected to a substitution reaction to form the compound V. The method provided by the invention has the characteristics of having a short route, wide applicability, relatively mild reaction conditions, a high reaction yield, and low costs, and being suitable for industrial scale-up production.

RECHERCES SUR LES SUBSTANCES MESOMORPHES-IX; SMECTIQUES "FOURCHUS". ORGANISATION MOLECULAIRE DANS LES PHASES SMECTIQUES

Malthete, Jacques,Canceill, Josette,Gabard, Jacqueline,Jacques, Jean

, p. 2823 - 2828 (2007/10/02)

The synthesis and the mesomorphic properties of new branched smectogenic A derivatives of fluorene are described.The observation that branched chain compounds from a smectic A phase allows conclusions to be drawn on molecular arrangements in smectic A layers.

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