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2-Ethyl-1,3-hexanediol

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CasNo: 94-96-2 Purity: Molecular Structure: C8H18O2

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2-Ethyl-1,3-hexanediol Basic Product Information

Product Name 2-Ethyl-1,3-hexanediol CAS 94-96-2
Synonyms 2-Ethyl-1,3-hexanediol;2-Ethyl-1,3-hexylene glycol;2-Ethyl-3-propyl-1,3-propanediol;2-Ethylhexanediol;3-Hydroxymethyl-n-heptan-4-ol;6-12;Diol-Kyowa 8;Ethohexadiol;NSC 3881;Octylene glycol;Repellent 612;Rutgers 612; Molecular Formula C8H18O2
EINECS Number 202-377-9 Molecular Structure
Appearance Light Yellow Powder
Purity
Supply Ability

2-Ethyl-1,3-hexanediol Quality documents

2-Ethyl-1,3-hexanediol Appearance/Package/Shipping/Storage

package

storage condition

Store in cool & dry place,Keep away from strong light and heat

2-Ethyl-1,3-hexanediol Application

2-Ethyl-1,3-hexanediol literature

Isolation and total synthesis of two novel metabolites from the fissurellid mollusc Scutus antipodes

Chand, Satish,Karuso, Peter

supporting information, p. 1020 - 1023 (2017/02/18)

There is almost no information on natural products from gastropods in the order Vetigastropoda and nothing at all for the superfamily Fissurellidae (keyhole and slit limpets), which are only partially protected from predation by their shell. Extraction of the Australian fissurellid Scutus antipodes yielded two new compounds, scutinin A [D-sorbityl hexakis(p-hydroxybenzoate)] and scutinin B [2-ethylhexane-1,3-bis(p-hydroxybenzoate)] that were identified by spectroscopic analysis and their structures confirmed by total synthesis. The compounds were found to have antimicrobial activity but no fish antifeedant activity.


Asymmetric cross- and self-aldol reactions of aldehydes in water with a polystyrene-supported triazolylproline organocatalyst

Llanes, Patricia,Sayalero, Sonia,Rodríguez-Escrich, Carles,Pericàs, Miquel A.

supporting information, p. 3507 - 3512 (2016/07/06)

A polystyrene (PS) immobilized triazolylproline has been prepared by a bottom-up approach involving co-polymerization with full regiocontrol. The resulting PS resin swells in water and has been applied to the enantioselective cross-aldol reaction and to the self-aldol reaction of aldehydes under essentially neat conditions, excellent yields and stereoselectivities being recorded.


Thermal decomposition of diethylketone cyclic triperoxide in polar solvents

Barreto, Gaston P.,Alvarez, Elida E.,Eyler, Gladys N.,Canizo, Adriana I.,Allegretti, Patricia E.

, p. 881 - 886 (2014/07/07)

The thermolysis of diethylketone cyclic triperoxide (3,3,6,6,9,9-hexaethyl- 1,2,4,5,7,8-hexaoxacyclononane, DEKTP) was studied in different polar solvents (ethanol, 2-propanol, 1-butanol, 2-butanol, 2-methyl-2-propanol, and acetonitrile). The rate constant values (kd) are higher for reactions performed in secondary alcohols probably because of the possibility to form a cyclic adduct with the participation of the hydrogen atom bonded to the secondary carbon. The kinetic parameters were correlated with the physicochemical properties of the selected solvents. The products of the DEKTP thermal decomposition in different polar solvents support a radical-based decomposition mechanism. CSIRO 2014.


Extracts of Isochrysis sp.

-

, (2010/04/25)

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.


2-Ethyl-1,3-hexanediol Upstream and downstream

94-96-2 Upstream product

  • 27970-80-5

    2-ethyl-1-hydroxy-3-hexanone 

  • 5659-15-4

    3-ethyl-4-propylidene-oxetan-2-one 

  • 33093-90-2

    3-benzyloxy-2-ethyl-hexan-1-ol 

  • 123-72-8

    butyraldehyde 

  • 71-36-3

    butan-1-ol 

  • 64-17-5

    ethanol 

  • 504-61-0

    (E)-but-2-enol 

  • 123-19-3

    4-heptanone 

94-96-2 Downstream Products

  • 99711-10-1

    5-ethyl-2-(4-tert-butyl-phenoxy)-4-propyl-[1,3,2]dioxaphosphorinane-2-oxide 

  • 10140-93-9

    chlorophosphoric acid-(2-ethyl-1-propyl-propanediyl ester) 

  • 71662-03-8

    3-benzyloxymethyl-heptan-4-ol 

  • 96794-65-9

    5-ethyl-2-phenyl-4-propyl-[1,3,2]dioxaborinane 

  • 71672-64-5

    3-(4-Methoxy-benzyloxymethyl)-heptan-4-ol 

  • 61478-22-6

    3-tert-butoxymethyl-heptan-4-ol 

  • 94124-36-4

    3-(tert-Butyl-methoxy-phenyl-silanyloxymethyl)-heptan-4-ol 

  • 114094-30-3

    3-(tert-Butoxy-diphenyl-silanyloxymethyl)-heptan-4-ol 

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