- CasNo6378-65-0
- Purity99%
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Quality products?make an important contribution to long-term revenue and profitability. Cost-effective and customizable Hexyl hexanoate 6378-65-0 in stock
1.What is the Hexyl hexanoate ?
Used in Flavor and Fragrance Industry:
Hexyl hexanoate is used as a flavoring agent for its sweet, fruity, and green aroma with tropical notes. It is particularly suitable for enhancing the taste and scent of various food products, such as fruits, jams, and beverages.
Used in Perfumery:
Hexyl hexanoate is used as a fragrance ingredient in the perfumery industry, where its herbaceous and tropical scent adds depth and complexity to perfume compositions.
Used in the Cosmetic Industry:
Hexyl hexanoate is used as a component in cosmetic formulations, such as lotions, creams, and shampoos, for its pleasant aroma and ability to provide a fresh, clean scent.
Used in the Food Industry:
Hexyl hexanoate is used as an additive in the food industry to impart a sweet, fruity, and green flavor to various products, such as fruit-flavored beverages, candies, and desserts.
Used in the Beverage Industry:
Hexyl hexanoate is used in the beverage industry to add a tropical, fruity, and green note to drinks, such as fruit juices, soft drinks, and alcoholic beverages like wine and cider.
Used in the Pharmaceutical Industry:
Hexyl hexanoate may be used in the pharmaceutical industry as a component in the development of drugs that target specific receptors or pathways, potentially leading to novel therapeutic applications.
-
-
66-25-1
hexanal
-
-
6378-65-0
n-hexyl caproate
-
-
142-62-1
hexanoic acid
-
-
111-27-3
hexan-1-ol
Conditions
| Conditions | Yield |
|---|---|
|
With
aluminum (III) chloride; triethylamine;
In
dichloromethane;
at 20 ℃;
for 48h;
|
84% 7% 7% |
|
With
aluminum (III) chloride; triethylamine;
In
dichloromethane;
at 20 ℃;
for 48h;
|
82% 82% 6% |
|
With
[Ru(H2O)2(phen)2](OTf)2; hydrogen;
In
sulfolane; water;
at 175 ℃;
for 3h;
under 56887.8 Torr;
|
81 %Chromat. 12 %Chromat. 7 %Chromat. |
-
-
111-27-3
hexan-1-ol
-
-
6378-65-0
n-hexyl caproate
Conditions
| Conditions | Yield |
|---|---|
|
With
C23H42N2OP2Ru;
for 12h;
Reflux;
Inert atmosphere;
Darkness;
|
100% |
|
Ru complex;
at 157 ℃;
for 24h;
Inert atmosphere;
|
99% |
|
With
calcium hypochlorite;
In
water; acetic acid; acetonitrile;
at 0 ℃;
for 1h;
|
98% |
|
With
pyridinium hydrobromide perbromide;
In
water;
at 20 ℃;
for 16h;
|
98% |
|
With
dihydrogen peroxide; bromine;
In
dichloromethane; water;
at 20 ℃;
for 6h;
|
98% |
|
With
sodium bromite;
In
water; acetic acid;
for 10h;
Ambient temperature;
|
96% |
|
With
sodium bromate;
hydrogen bromide;
In
tetrachloromethane;
at 35 - 37 ℃;
for 2h;
|
96% |
|
With
disodium hydrogenphosphate; benzyltrimethylammonium tribromide;
In
tetrachloromethane; water;
at 60 ℃;
for 5h;
|
96% |
|
With
sodium bromate; sulfuric acid; sodium bromide;
In
water;
at 20 ℃;
for 24h;
|
96% |
|
With
N-Bromosuccinimide; L-proline;
In
water;
at 20 ℃;
for 1h;
|
94% |
|
With
[bis(2-methylallyl)cycloocta-1,5-diene]ruthenium(II); (2-((2-(diphenylphosphanyl)ethyl)(quinolin-2-ylmethyl)amino)ethyl)diphenylphosphine oxide; potassium tert-butylate;
In
n-heptane;
at 100 ℃;
for 16h;
Reagent/catalyst;
Solvent;
|
93% |
|
With
tris((2-(diphenylphosphino)ethyl)amino)ruthenium monocarbonyl;
In
toluene;
for 18h;
Glovebox;
Schlenk technique;
Inert atmosphere;
Reflux;
|
93% |
|
With
peracetic acid; sodium bromide;
In
ethyl acetate;
at 39.9 ℃;
for 2h;
|
92% |
|
With
oxygen;
at 60 ℃;
for 24h;
under 760.051 Torr;
Irradiation;
|
92% |
|
With
C29H44Cl2N2Ru; potassium tert-butylate;
In
toluene;
for 24h;
Reflux;
|
91% |
|
With
sulfuric acid; dihydrogen peroxide;
sodium tungstate;
In
water; acetonitrile;
at 80 ℃;
for 6h;
|
90% |
|
With
Hoveyda-Grubbs catalyst second generation; potassium hydroxide; tricyclohexylphosphine;
In
toluene;
at 110 ℃;
for 12h;
Reagent/catalyst;
Schlenk technique;
Inert atmosphere;
|
88% |
|
With
air;
[IrCl(coe)2]2;
at 95 ℃;
for 15h;
|
86% |
|
With
C24H29ClN4ORu; potassium hydroxide;
In
toluene;
at 110 ℃;
for 24h;
|
84% |
|
With
lead(IV) acetate; potassium bromide;
at 20 ℃;
for 4h;
|
83% |
|
With
[RuH(η2-BH4)(2-di-tert-butylphosphinomethyl-6-diethylaminomethylpyridine)];
In
toluene;
at 115 ℃;
for 24h;
Inert atmosphere;
|
77% |
|
With
C36H32Cl2N2O2P2Ru; sodium hydroxide;
In
toluene;
at 150 ℃;
for 16h;
Inert atmosphere;
Schlenk technique;
|
77% |
|
With
potassium phosphate; oxygen;
In
n-heptane;
at 120 ℃;
for 24h;
under 750.075 Torr;
Schlenk technique;
Green chemistry;
|
71% |
|
In
neat (no solvent);
at 180 ℃;
for 36h;
Inert atmosphere;
Green chemistry;
|
69% |
|
With
pyridine; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; trichloroisocyanuric acid;
In
acetonitrile;
Inert atmosphere;
|
68% |
|
With
tert.-butylhydroperoxide; sodium chloride; sodium hydroxide;
In
water;
at 70 ℃;
Sealed tube;
Green chemistry;
|
67% |
|
With
[bis({2‐[bis(propan‐2‐yl)phosphanyl]ethyl})amide](carbonyl)(hydride)iron(II);
In
toluene;
at 120 ℃;
for 20h;
Schlenk technique;
Inert atmosphere;
|
60% |
|
With
chromium(VI) oxide; aluminum oxide; water;
|
52% |
|
With
calcium bromate; hydrogen bromide;
at 35 ℃;
|
|
|
With
pyridine; tetrachloromethane; tert-butylhypochlorite;
|
|
|
at 220 - 310 ℃;
|
|
|
With
dihydridotetrakis(triphenylphosphine)ruthenium;
In
toluene;
at 180 ℃;
for 24h;
Yield given;
|
|
|
With
iodine;
hexachloroplatinate(II);
In
water;
|
|
|
Rhodococcus equi;
In
2,2,4-trimethylpentane;
at 30 ℃;
for 48h;
Yield given;
|
|
|
With
cerium (IV) sulfate tetrahydrate; lithium bromide;
In
water;
at 20 ℃;
|
96 %Chromat. |
|
With
cerium(III) nitrate hexahydrate; dihydrogen peroxide; lithium bromide;
In
water;
at 65 - 70 ℃;
|
84 %Chromat. |
|
With
trans-carbonyldihydrido(bis(2-(diisopropylphosphanyl)ethyl)amine)osmium;
at 157 ℃;
for 5h;
|
|
|
With
C28H37ClOOsP2; oxygen;
In
toluene;
at 120 ℃;
for 45h;
under 760.051 Torr;
|
99 %Chromat. |
|
With
N,N,N',N'-Tetraethylethylenediamine; Ru(PPh3)2(OAc)2;
at 157 ℃;
for 48h;
Inert atmosphere;
|
69 %Chromat. |
|
With
C19H31N3O2PRu;
at 160 ℃;
for 24h;
Inert atmosphere;
|
|
|
With
C25H35N2OPRu;
In
neat (no solvent);
at 110 ℃;
for 48h;
Reagent/catalyst;
Time;
Solvent;
Inert atmosphere;
Schlenk technique;
Glovebox;
|
26 %Chromat. |
|
With
C44H35ClO4P2Ru; caesium carbonate;
In
5,5-dimethyl-1,3-cyclohexadiene;
for 24h;
Inert atmosphere;
Reflux;
|
90 %Spectr. |
|
With
(PPhenP-H)RuH;
In
(2)H8-toluene;
for 6h;
Inert atmosphere;
Reflux;
|
99 %Chromat. |
|
With
bis[dichloro-(1,5-cyclooctadiene)ruthenium(2+)]; 1-butyl-3-methylimidazolium chloride; potassium hydroxide;
at 180 ℃;
for 20h;
under 760.051 Torr;
|
|
|
With
dihydrogen peroxide; cerous nitrate; lithium bromide;
In
water;
at 65 - 70 ℃;
|
|
|
With
trans-[(trans-[(diisopropylphosphino(2-picolyl)phosphine)2RuCl2])2RuCl2]; potassium tert-butylate;
In
m-xylene; toluene;
for 120h;
Schlenk technique;
Inert atmosphere;
Reflux;
|
37.6 %Chromat. |
|
With
oxygen;
at 55 ℃;
for 24h;
under 760.051 Torr;
Irradiation;
Sealed tube;
Green chemistry;
|
75 %Chromat. |
|
With
oxygen; sodium hydroxide;
at 45 ℃;
for 24h;
under 760.051 Torr;
Catalytic behavior;
|
> 99 %Chromat. |
|
With
1-butyl-3-methylimidazolium chloride; potassium hydroxide;
at 180 ℃;
for 20h;
|
|
|
With
(2,6-bis(di-tert-butylphosphinito)pyridine)RuH(Cl)(CO); potassium hydroxide;
at 157 ℃;
for 36h;
Reagent/catalyst;
Catalytic behavior;
Inert atmosphere;
|
|
|
With
(bis[(2-diisopropylphosphino)ethyl]amine)Mn(CO)2;
at 150 ℃;
for 24h;
Reagent/catalyst;
Temperature;
Catalytic behavior;
Inert atmosphere;
|
92 %Spectr. |
|
With
potassium tert-butylate;
In
diethyl ether;
at 45 ℃;
for 96h;
Reagent/catalyst;
Reflux;
Inert atmosphere;
|
97 %Chromat. |
|
With
bromopentacarbonylmanganese(I); potassium tert-butylate; N,N-bis-(3-dimethylaminopropyl)amine;
In
toluene;
at 110 ℃;
Schlenk technique;
Sealed tube;
Inert atmosphere;
|
36 %Chromat. |
|
With
C43H42NOP3Ru;
In
benzene;
at 135 ℃;
for 18h;
Inert atmosphere;
Glovebox;
Schlenk technique;
|
|
|
With
ruthenium(bis[2‐(ethylsulfanyl)ethyl]amine)(dichloro)(triphenylphosphine); potassium tert-butylate;
In
toluene;
at 110 ℃;
for 24h;
Inert atmosphere;
|
16 %Spectr. |
|
With
C30H43ClCoN2P3(1+)*Cl(1-); potassium tert-butylate;
In
toluene;
at 140 ℃;
for 24h;
Inert atmosphere;
Sealed tube;
|
82 %Chromat. |
|
With
2,5-dimethyl-1-octyl-1H-pyrrole; C28H41NOP2Ru;
In
toluene;
at 150 ℃;
for 24h;
Inert atmosphere;
Glovebox;
|
72 %Chromat. |
|
With
calcium bromate; hydrogen bromide;
at 35 ℃;
|
|
|
With
[Ru((PPh2CH2(C6H3N)CH2N=PCy3))ClH(PPh3)]; potassium hexamethylsilazane;
at 157 ℃;
for 24h;
Catalytic behavior;
Inert atmosphere;
Schlenk technique;
Glovebox;
|
|
|
With
RuH(CO)Cl(PPh3)(κ2-CP); caesium carbonate;
In
toluene;
at 110 ℃;
for 26h;
Schlenk technique;
Glovebox;
Inert atmosphere;
|
95 %Spectr. |
|
With
RuH(NC5H3(NP(C(CH3)3)2)COCH2C(CH3)2N)(CO);
at 160 ℃;
for 24h;
Reagent/catalyst;
Temperature;
Schlenk technique;
Inert atmosphere;
|
|
|
With
C22H30ClN4OPRu; potassium tert-butylate;
In
neat (no solvent);
at 150 ℃;
for 36h;
Temperature;
Catalytic behavior;
Inert atmosphere;
|
88 %Chromat. |
|
With
[2-bis(diphenylphosphinoethyl)aminato]carbonylhydrido(trimethylphosphine)ruthenium(II);
In
toluene;
at 135 ℃;
Reagent/catalyst;
Kinetics;
Catalytic behavior;
Inert atmosphere;
Schlenk technique;
Sealed tube;
|
2.What is the CAS number for Hexyl hexanoate ?
The CAS number of Hexyl hexanoate is 6378-65-0.
More information of Hexyl hexanoate 6378-65-0 are:
|
CAS?Number |
6378-65-0 |
|
Density |
0.863 g/cm3 |
|
Melting Point |
-55 °C |
|
Boiling Point |
246 °C at 760 mmHg |
|
Flash Point |
99.4 °C |
|
Vapor Pressure |
0.0278mmHg at 25°C |
|
Refractive Index |
n20/D 1.424(lit.) |
|
HS CODE |
29159000 |
|
PSA |
26.30000 |
|
LogP |
3.69020 |
3.What are another words for Hexyl hexanoate ?
Synonyms?for?Hexyl hexanoate 6378-65-0:1-Hexylcaproate;1-Hexyl hexanoate;Hexyl caproate;Hexyl hexanoate;Hexyl hexoate;NSC 53799;n-Hexyl hexanoate;n-Hexyl n-hexanoate;AI3-06035;BRN 1762037;
4.What is the molecular formula of Hexyl hexanoate?
The chemical formula of ?Hexyl hexanoate is?C12H24O2 which containing 12 Carbon atoms,24 Hydrogen atoms and 2 Oxygen atoms,and the molecular weight of??Hexyl hexanoate?is 200.321.
5.What is Hexyl hexanoate (6378-65-0) used for?
Hexyl hexanoate has a herbaceous odor. May be synthesized by passing n-hexyl alcohol over CuO + UO3 catalyst at 220 - 310°C, or by treating n-hexyl alcohol with Ca(Br03)2 and diluted aqueous HBr at 30°C.
InChI:InChI=1/C12H24O2/c1-3-5-7-9-11-14-12(13)10-8-6-4-2/h3-11H2,1-2H3
Relevant articles related to Hexyl hexanoate:
|
Article |
Source |
|
Disproportionation of aliphatic and aromatic aldehydes through Cannizzaro, Tishchenko, and Meerwein–Ponndorf–Verley reactions |
Sharifi, Sina,Sharifi, Hannah,Koza, Darrell,Aminkhani, Ali , p. 803 - 808 (2021/07/20) |
|
The key role of the latent N-H group in Milstein's catalyst for ester hydrogenation |
Chianese, Anthony R.,He, Tianyi,Jarczyk, Cole E.,Keith, Jason M.,Kelly, Sophie. E.,Kim, Thao,Pham, John,Reynolds, Eamon F. , p. 8477 - 8492 (2021/06/28) |
6.Buy Hexyl hexanoate with the best price .
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