23433-05-8

Usage

Uses

Used in Skincare and Cosmetics Industry:
1,3-Octanediol is used as a humectant and emollient for its ability to attract and retain moisture in the skin, providing hydration and improving skin texture.
Used in Personal Care Industry:
1,3-Octanediol is used as an antimicrobial agent in products such as deodorants, hair care products, and lotions, helping to prevent the growth of bacteria and maintain a clean and healthy environment for the skin.
Used in Chemical Manufacturing:
1,3-Octanediol is utilized in the production of other chemicals, contributing to the synthesis of various compounds used in different industries.
Used as a Solvent:
In various applications, 1,3-Octanediol serves as a solvent, aiding in the dissolution of other substances and facilitating chemical reactions.

InChI:InChI=1/C8H18O2/c1-2-3-4-5-8(10)6-7-9/h8-10H,2-7H2,1H3

Upstream product

• 592-76-7 1-Heptene 
• 50-00-0 formaldehyd 
• 1906-95-2 5-bromopentylmalonic acid diethyl ester 
• 7786-52-9 1-hydroxyoctan-3-one 
• 22348-95-4 methyl 3-oxooctanoate 
• 6085-30-9 1-acetoxy-octan-3-one 

Downstream Products

• 202188-43-0 2-methyl-4-pentyl-1,3-dioxane 
• 202188-43-0 2-methyl-4-pentyl-1,3-dioxane 
• 202188-43-0 (2R,4R)-2-methyl-4-pentyl-1,3-dioxane 
• 202188-43-0 (2S,4R)-2-methyl-4-pentyl-1,3-dioxane 
• 202188-43-0 (2R,4S)-2-methyl-4-pentyl-1,3-dioxane 
• 202188-43-0 (2S,4S)-2-methyl-4-pentyl-1,3-dioxane 
• 101691-96-7 2-(p-Toluenesulfonyloxy)octan-3-ol 
• 1311463-07-6 1-(benzyloxy)octan-3-one 
• 1311463-14-5 ((3,3-difluorooctyloxy)methyl)benzene 
• 170798-94-4 1-(benzyloxy)octan-3-ol 

Relevant academic research and scientific papers

Aliphatic β-D-glucosides from fruits of Carica pubescens

Ethyl 3-O-β-D-glucopyranosylbutanoate, butyl 3-O-β-D- glucopyranosylbutanoate and 3-oxo-octyl 1-O-β-D-glucopyranoside were isolated from Carica pubescens fruit pulp by liquid chromatography on XAD. Identifications were performed after peracetylation by comparison of HRGC and HRGC-mass spectral data with those of synthesized reference compounds. Chiral evaluation of glycosidically-bound 3-hydroxybutanoates and octane-1,3-diol was achieved by multidimensional gas chromatography, combining a polar achiral column (DB-Wax) with a chiral main column (heptakis-2,6-di-O-methyl- 3-O-pentyl-β-cyclodextrin/OV 1701 and 2.3-di-O-acetyl-6-O-tert-butyl- dimethylsilyl-β-cyclodextrin/OV 1701, respectively). Comparison of retention times of synthesized, optically-enriched reference compounds with enzymically-released aglycones revealed enantiomeric excesses of the (S)-3- hydroxybutanoates, i.e. 96% and 24%, for the ethyl and the butyl ester, respectively. Octane-1,3-diol exhibited an enantiomeric excess of (R)-90%.

IDENTIFICATION OF 3-HYDROXYOCTYL β-D-GLUCOSIDE AND ABSOLUTE CONFIGURATION OF FREE AND BOUND OCTANE-1,3-DIOL IN APPLE FRUIT

In an extract obtained from neutralized apple juice, cv.Jonathan, by LC separation on Amberlite XAD resin using ethyl acetate elution , 3-hydroxyoctyl β-D-glucoside was identified by HRGC, HRGC-MS and HRGC-FTIR after per-O-methylation.Chiral evaluation of free and glucosidically bound octane-1,3-diol was performed by HRGC after derivatization with Mosher's reagent revealing the occurrence of optically pure diol in apple fruit.By means of comparison of optical rotation of the 1,3-diacetoxy derivative with previously published data, (R)-(+)-configuration was evaluated.Key Word Index - Malus sylvestris; Rosaceae; apple; fruit; 3-hydroxyoctyl β-D-glucoside; free and bound (R)-(+)-octane-1,3-diol.

Regio-selective hydroxylation of gem-difluorinated octanes by alkane hydroxylase (AlkB)

gem-Difluoromethylene substituted molecules constitute a distinct class of fluorinated compounds. In this study, special chemistry has been developed for their preparation based on the highly selective terminal hydroxylation of these gem-difluorinated oct

Extracts of Isochrysis sp.

The present invention relates to extracts of Isochrysis sp., preferably Tahitian Isochrysis, its cosmetic, dermatological and/or therapeutic uses and compositions and cosmetic, dermatological or therapeutic products comprising such an extract of Isochrysis sp., preferably Tahitian Isochrysis.

Extracts of isochrysis sp.

The present invention relates to extracts of Isochrysis sp., preferably Tahitian Isochrysis, its cosmetic, dermatological and/or therapeutic uses and compositions and cosmetic, dermatological or therapeutic products comprising such an extract of Isochrysis sp., preferably Tahitian Isochrysis.

EXTRACTS OF TETRASELMIS SP.

The present invention relates to extracts of Tetraselmis sp., preferably Tetraselmis suecica, its cosmetic, dermatological and/or therapeutic uses and compositions and cosmetic, dermatological or therapeutic products comprising such an extract of Tetraselmis sp., preferably Tetraselmis suecica.

Extracts of Tetraselmis sp. for cosmetic and therapeutic purposes

The present invention relates to extracts of Tetraselmis sp., preferably Tetraselmis suecica, its cosmetic, dermatological and/or therapeutic uses and compositions and cosmetic, dermatological or therapeutic products comprising such an extract of Tetraselmis sp., preferably Tetraselmis suecica.

Synthese de l'acide (dimercapto-1,3 propyl-2)-15 pentadecanoique, complexant potentiel du 99mTc

The synthesis of 15-(1,3-dimercapto 2-propyl) pentadecanoic acid was performed in ten steps.One of these steps is the condensation of (5) with 7-bromoheptanoic acid.It is achieved in liquid ammonia or in a HMPA-THF medium with yields higher than 50 percent.In the second case a-5 bromoacid-ratio of 2.1 (slightly superior to the stoichiometry) is sufficient to obtain these yields, whereas in ammonia, the ratio must be higher than 5 and is therefore clearly unfavourable.The reaction times are also much longer in ammonia.The obtention of 5 from diethyl (6-bromohexyl) malonate 2 implies the reduction of ester functions and the substitution of Br by the ethynyl group.The optimal conditions and the sequence of these two steps have been determined.

Interphenylene carbacyclin derivatives

A compound of the formula STR1 and intermediates useful in preparing same.