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PRISTANE Good Supplier In Bulk Supply High Purity 1921-70-6
- Molecular Formula: C19H40
- Molecular Weight: 268.527
- Vapor Pressure: 0.0026mmHg at 25°C
- Melting Point: -99 °C
- Refractive Index: n20/D 1.438(lit.)
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Boiling Point:
68 °C0.001 mm Hg(lit.)
- Flash Point: 110 °C
- PSA: 0.00000
- Density: 0.783 g/mL at 20 °C(lit.)
- LogP: 7.08150
PRISTANE(Cas 1921-70-6) Usage
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Biochem/physiol Actions |
Pristane is a hydrocarbon oil adjuvant widely used to induce tumorigenesis in mice and arthritis and lupus nephritis in rats. It works as a adjuvant for monoclonal antibody generation in mouse ascites. |
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Purification Methods |
Purify pristane by shaking it with conc H2SO4 (care, if amount of pristane is too small then it should be diluted with pet ether not Et2O which is quite soluble H2SO4), then H2O (care, as it may heat up in contact with conc H2SO4), dry (MgSO4), evaporate and distil it over Na. [S.rensen & S.rensen Acta Chem Scand 3 939 1949, Beilstein 1 III 570.] |
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Definition |
ChEBI: A norterpene that is an acyclic saturated hydrocarbon derived from phytane by loss of its C-16 terminal methyl group. |
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General Description |
Pristane is a natural saturated terpenoid alkane used in research on the pathogenesis of autoimmune diseases such as arthritis and lupus. |
InChI:InChI=1/C19H40/c1-16(2)10-7-12-18(5)14-9-15-19(6)13-8-11-17(3)4/h16-19H,7-15H2,1-6H3
1921-70-6 Relevant articles
Class II histocompatibility complex expression enhancing compound and preparation method and application thereof
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Paragraph 0099-0102, (2021/08/28)
The invention discloses a class II histo...
Greener synthesis of pristane by flow dehydrative hydrogenation of allylic alcohol using a packed-bed reactor charged by pd/c as a single catalyst
Fukuyama, Takahide,Furuta, Akihiro,Hirobe, Yuki,Hyodo, Mamoru,Kasakado, Takayoshi,Ryu, Ilhyong
, (2021/10/05)
Our previous work established a continuo...
Flow Dehydration and Hydrogenation of Allylic Alcohols: Application to the Waste-Free Synthesis of Pristane
Furuta, Akihiro,Hirobe, Yuki,Fukuyama, Takahide,Ryu, Ilhyong,Manabe, Yoshiyuki,Fukase, Koichi
supporting information, p. 1365 - 1368 (2017/03/23)
Hydroxy-substituted sulfonic acid functi...
The formation features of C10–C20 regular petroleum isoprenanes
Gordadze,Giruts,Poshibaeva,Koshelev
, p. 672 - 676 (2016/10/04)
To model the formation processes of C10–...
1921-70-6 Process route
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253686-88-3,844467-91-0
(E)-3,7,11,15-tetramethylhexadec-2-en-1-ol
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6864-53-5
norfarnesane
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2051-30-1
2,6-dimethyloctane
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3891-98-3
2,6,10-trimethyldodecane
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1921-70-6
pristane
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17302-28-2
2,6-Dimethylnonane
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17301-23-4
2,6-dimethyl-undecane
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3891-99-4
2,6,10-trimethyl tridecane
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3892-00-0
norpristane
| Conditions | Yield |
|---|---|
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at 330 - 400 ℃;
for 6h;
Sealed tube;
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45316-02-7
2,6,10,14,19,23,27,31-octamethyldotriacontane
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6864-53-5
norfarnesane
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2051-30-1
2,6-dimethyloctane
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3891-98-3
2,6,10-trimethyldodecane
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-
1921-70-6
pristane
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17302-28-2
2,6-Dimethylnonane
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638-36-8
phytane
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17301-23-4
2,6-dimethyl-undecane
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3891-99-4
2,6,10-trimethyl tridecane
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3892-00-0
norpristane
| Conditions | Yield |
|---|---|
|
at 330 - 400 ℃;
for 6h;
Sealed tube;
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1921-70-6 Upstream products
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21980-66-5
2,6,10,14-tetramethyl-2-pentadecanol
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2140-82-1
2,6,10,14-tetramethyl-1-pentadecene
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645-72-7
3,7,11,15-tetramethyl-hexadecanol
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925694-14-0
2,6,10,14-tetramethyl-pentadeca-2,6,10,12-tetraene
1921-70-6 Downstream products
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21980-66-5
2,6,10,14-tetramethyl-2-pentadecanol
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104000-14-8
2,6,10,14-tetramethyl-6-pentadecanol
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14035-81-5
ethylsuccinic anhydride
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875-29-6
2,3-diethyl-succinic acid anhydride
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