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111-02-4

111-02-4 Structure

111-02-4 Structure
IdentificationMore
[Name]

(all-E)-2,6,10,15,19,23-Hexamethyl-2,6,10,14,18,22-tetracosahexaene
[CAS]

111-02-4
[Synonyms]

2,6,10,15,19,23-HEXAMETHYL-2,6,10,14,18,22-TETRACOSAHEXAENE
2,6,10,15,19,23-HEXAMETHYL-2, 6, 10, 14, 18, 22-TETRACOSAHEXENE
(all-e)-2,6,10,15,19,23-hexamethyl-2,6,10,14,18,22-tetracosahexaene
(E,E,E,E)-Squalene
SPINACENE
SQUALENE
SQUALENE OIL
trans-squalene
(6E,10E,14E,18E)-2,6,10,15,19,23-Hexamethyl-2,6,10,14,18,22-tetracosahexaene
14,18,22-tetracosahexaene,2,6,10,15,19,23-hexamethyl-(all-e)-10
2,6,10,15,19,23-hexamethyltetracosa-
2,6,10,15,19,23-Hexamethyltetracosa-2,6,10,14,18,22-hexaene
2,6,10,15,19,23-hexamethyl-tetracosa-2,6,10,14,18,22-hexane
2,6,10,15,19,23-Hexamethyltetracosahexa-2,6,10,14,18,22-ene
6,10,14,18,22-Tetracosahexaene,2,6,10,15,19,23-hexamethyl-,(all-E)-2
All-trans-Squalene
Spinacen
Squalen
Supraene
trans-Spinacene
[EINECS(EC#)]

203-826-1
[Molecular Formula]

C30H50
[MDL Number]

MFCD00008912
[Molecular Weight]

410.72
[MOL File]

111-02-4.mol
Chemical PropertiesBack Directory
[Appearance]

clear colourless to faint yellow oil
[Melting point ]

−75 °C(lit.)
[Boiling point ]

285 °C25 mm Hg(lit.)
[density ]

0.858 g/mL at 25 °C(lit.)
[vapor pressure ]

0Pa at 25℃
[refractive index ]

n20/D 1.494(lit.)
[Fp ]

>230 °F
[storage temp. ]

2-8°C
[solubility ]

DMSO : 16.67 mg/mL (40.59 mM; Need ultrasonic)H2O : < 0.1 mg/mL (insoluble)
[form ]

liquid
[color ]

light yellow
[Odor]

oil, faint odor
[biological source]

animal
[Water Solubility ]

<0.1 g/100 mL at 19 ºC
[Merck ]

14,8768
[BRN ]

1728919
[Major Application]

environmental
food and beverages
[Cosmetics Ingredients Functions]

SOLVENT
SKIN CONDITIONING - EMOLLIENT
HAIR CONDITIONING
[InChI]

1S/C30H50/c1-25(2)15-11-19-29(7)23-13-21-27(5)17-9-10-18-28(6)22-14-24-30(8)20-12-16-26(3)4/h15-18,23-24H,9-14,19-22H2,1-8H3/b27-17+,28-18+,29-23+,30-24+
[InChIKey]

YYGNTYWPHWGJRM-AAJYLUCBSA-N
[SMILES]

CC(C)=CCCC(C)=CCCC(C)=CCC\C=C(/C)CCC=C(C)CCC=C(C)C
[LogP]

14.12 at 24℃
[CAS DataBase Reference]

111-02-4(CAS DataBase Reference)
[NIST Chemistry Reference]

2,6,10,14,18,22-Tetracosahexaene, 2,6,10,15,19,23-hexamethyl-, (all-E)-(111-02-4)
[EPA Substance Registry System]

111-02-4(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Health Hazard (GHS08)
GHS08
[Signal word ]

Danger
[Hazard statements ]

H304
[Precautionary statements ]

P301+P310+P331
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

2
[RTECS ]

XB6010000
[F ]

8-10-23
[TSCA ]

Yes
[REACH Registrations]

Active
[HS Code ]

29012980
[Storage Class]

10 - Combustible liquids
[Hazard Classifications]

Asp. Tox. 1
[Hazardous Substances Data]

111-02-4(Hazardous Substances Data)
[Toxicity]

mouse,LD50,intravenous,1800mg/kg (1800mg/kg),Japanese Journal of Cancer Research. Vol. 76, Pg. 1021, 1985.
Raw materials And Preparation ProductsBack Directory
[Raw materials]

(2S)-1-(3-Acetylthio-2-methyl-1-oxopropyl)-L-proline-->Squalene-->Oils, shark-liver-->Squalane
[Preparation Products]

Cyclohexane, 1,1-dimethyl-3-methylene-2-[(3E,7E,11E)-3,8,12,16-tetramethyl-3,7,11,15-heptadecatetraenyl]-, (2S)- (9CI)-->HEXAEPOXYSQUALENE
Hazard InformationBack Directory
[General Description]

Clear, slightly yellow liquid with a faint odor. Density 0.858 g/cm3.
[Reactivity Profile]

TRANS-SQUALENE(111-02-4) is incompatible with strong oxidizing agents. .
[Air & Water Reactions]

May become discolored on exposure to air. Insoluble in water.
[Health Hazard]

ACUTE/CHRONIC HAZARDS: When heated to decomposition this compound emits toxic fumes of carbon monoxide and carbon dioxide.
[Fire Hazard]

This chemical is probably combustible.
[Chemical Properties]

clear colourless to faint yellow oil
[Uses]

Bactericide; intermediate in manufacture of pharmaceuticals, organic coloring materials, rubber chemicals, aromatics and surface active agents.
[Uses]

cosmetic and pharmaceutical excipient
[Uses]

Squalene is a natural triterpene that plays an important role in the synthesis of cholesterol, steroid hormones, and vitamin D in the human body. Squalene is commonly used as a biochemical precursor i n the preparation of steroids. Squalene is also a natural moisturizer with low acute toxicity and is not significant human skin irritants or sensitizers.
[Definition]

ChEBI: A triterpene consisting of 2,6,10,15,19,23-hexamethyltetracosane having six double bonds at the 2-, 6-, 10-, 14-, 18- and 22-positions with (all-E)-configuration.
[Production Methods]

Squalene is extracted from shark liver or synthesized from hexaphenyl-1,4-butanediyldiphosphonium dibromide and 6,10-dimethyl-5,9-undecadien-2-one (geranylacetone, industrial intermediate in the vitamin E synthesis).
[Flammability and Explosibility]

Nonflammable
[Biochem/physiol Actions]

Squalene is a biosynthetic precursor to all steroids. It acts as a cytoprotective agent to normal cells exposed to carcinogens and antitumor agents. Squalene helps in equalizing the blood cholesterol levels. It increases the production of HDL (high density lipoprotein) and the excretion of LDL (low density lipoprotein). This helps in reducing the risk of heart disease and protects the less stable body fats from oxidation. It is also used in treating hypercholesterolemia. Squalene is known to improve the efficiency of cholesterol lowering drugs. It also serves as an antioxidant by preventing the effects of free radical. It protects skin from drying and other environmental conditions such as oxidation, ultraviolet rays and pollutants. Squalene is known to promote wound healing.
[target]

COX | STAT | FOXP3 | Nrf2 | SOD | GPx
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

(all-E)-2,6,10,15,19,23-Hexamethyl-2,6,10,14,18,22-tetracosahexaene(111-02-4).msds
Spectrum DetailBack Directory
[Spectrum Detail]

Squalene(111-02-4)1HNMR
Squalene(111-02-4)IR1
Squalene(111-02-4)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Squalene, 99+%(111-02-4)
[Alfa Aesar]

Squalene, 98%(111-02-4)
[Sigma Aldrich]

111-02-4(sigmaaldrich)
[TCI AMERICA]

Squalene,>96.0%(GC)(111-02-4)
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