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Chemical Structure| 1921-70-6 Chemical Structure| 1921-70-6

Structure of Pristane
CAS No.: 1921-70-6

Chemical Structure| 1921-70-6

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Pristane is a naturally occurring saturated alkane found in small amounts in plants and marine organisms. It is widely used to induce immune responses in rats and mice and is a non-antigenic adjuvant that induces MHC II restricted arthritis T cells in rats.

Synonyms: Norphytane

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Product Details of Pristane

CAS No. :1921-70-6
Formula : C19H40
M.W : 268.52
SMILES Code : CC(CCCC(CCCC(CCCC(C)C)C)C)C
Synonyms :
Norphytane
MDL No. :MFCD00008952

Safety of Pristane

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
RAW264.7 cells 12.5–200 ng/ml 24 hours Investigated the effect of Pristane on TremL4 expression, showing that Pristane dose-dependently enhanced TremL4 staining Elife. 2022 Oct 20;11:e76205

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice SJL/J mice Intraperitoneal injection 0.5 mL Single injection, observed for 16 weeks To study the impact of Xist RNP on autoimmune pathology in the pristane-induced SLE model. Results showed that pristane injection coupled with tgXist expression in males led to higher incidence and severity of glomerulonephritis, hepatic lipogranulomas, and pulmonary hemorrhage, reflecting disease damage observed in severe SLE patients. Cell. 2024 Feb 1;187(3):733-749. e16
BALB/c mice Pristane-induced SLE model Intraperitoneal injection 0.5 mL Single injection, lasted for 24 weeks The pristane-induced SLE model simulates human SLE manifestations, including proteinuria, serositis, and glomerulonephritis. Dietary OLA supplementation improved kidney damage and endothelial dysfunction. Antioxidants (Basel). 2023 Jun 19;12(6):1303
C57BL/6 mice Pristane-induced lupus nephritis model Intraperitoneal injection 0.5 mL Single injection To induce lupus nephritis model, results showed that pristane injection led to increased proteinuria, renal function impairment, and renal pathological changes. Front Immunol. 2021 Jul 5;12:683249.
C57BL/6 mice Pristane-induced DAH model Intraperitoneal injection 0.5 mL Single injection, observed until day 14 To evaluate the therapeutic potential of miR-146a in DAH. Results showed that intra-pulmonary miR-146a delivery could suppress DAH by reducing TRAF6, IL-8, NETs and apoptosis expression. J Biomed Sci. 2022 Aug 26;29(1):62
Mice CD38-deficient mice Intraperitoneal injection 0.5 mL Single dose, observed for 2 weeks To study pristane-induced lupus-like disease, finding that CD38-deficient mice showed milder inflammatory responses compared to wild-type mice Front Immunol. 2022 Oct 24;13:1013236
Mice (C57BL/6 background) Pristane-induced lupus model Intraperitoneal injection 0.5 mL Single injection, observed for 10 months To evaluate the impact of OGG1 deficiency on lupus-like inflammatory responses, showing enhanced inflammation and skin pathology in Ogg1?/? mice Front Immunol. 2020 Sep 24;11:554725
Mice Pristane-induced diffuse alveolar hemorrhage model Intraperitoneal injection 0.5 mL Single injection, observed for 7 days To evaluate the role of ER stress in pristane-induced lung injury. Results showed increased expression of ER stress markers (e.g., Chop and Bip) in the lungs of pristane-treated mice, correlating with neutrophil infiltration. Front Immunol. 2022 Feb 3;13:790043
Mice Pristane-induced lupus model Intraperitoneal injection 0.5 mL Single injection, observed for 6 months Study the role of autophagy in the maintenance of autoreactive memory B cells and lupus development Front Immunol. 2021 Jul 16;12:701066
C57BL/6 mice Pristane-induced lupus model Intraperitoneal injection 0.5 mL Single injection, observed for 14 days Studied the effect of Pristane on monocyte differentiation and DAH, showing that Pristane treatment increased circulating Ly6C?CD138+ monocytes, associated with DAH susceptibility Elife. 2022 Oct 20;11:e76205
CBA/Igb mice Pristane-induced arthritis model Intraperitoneal injection 0.5 mL Two injections, 50 days apart To investigate whether Pristane-induced arthritis is dependent on CD4+ T cells. Results showed that Pristane-induced arthritis depends on the presence of CD4+ T cells. Immunology. 1997 Jan;90(1):81-6
C57BL/6 mice Pristane-induced acute SLE-like lung inflammation model Intraperitoneal injection 0.5 mL Single injection, observed at 3, 7, and 14 days To evaluate the effect of Pristane on lung inflammation, results showed that Pristane treatment led to reduced miR-125a expression, enhanced IL-16 expression, and increased neutrophil infiltration in the lungs. JCI Insight. 2018 Aug 9;3(15):e120798
BALB/c mice Pristane-induced lupus model Intraperitoneal injection 0.5 mL Single injection Induce lupus-like disease and evaluate cognitive impairment and features of neuropsychiatric lupus Int J Mol Sci. 2024 Dec 5;25(23):13080
BALB/c mice Pristane-induced lupus model Intraperitoneal injection 0.5 mL Single injection, observed at 1, 2, 4, or 8 months To investigate whether the pristane-induced lupus model is suitable for neuropsychiatric lupus (NPSLE) studies. Results showed that PIL mice exhibited olfactory dysfunction, anxiety- and depression-like behavior, and pathological changes in the brain. Behav Brain Funct. 2023 Feb 10;19(1):3
BALB/c mice Pristane induced lupus mouse model Intraperitoneal injection 0.5 mL Single injection, lasting for 4 months To study the effects of Pristane-induced lupus mouse model on neuroinflammation and behavioral deficits. Results showed that Pristane-induced lupus mice exhibited olfactory dysfunction, anxiety- and depression-like behaviors, as well as neuroinflammation and brain pathological changes. Behav Brain Funct. 2023 Jun 15;19(1):11
C57BL/6 mice Pristane-induced SLE model Intraperitoneal injection 0.5mL Single injection, sacrificed on Day 7 To evaluate the effect of GSK-J4 on ISG expression in the Pristane-induced SLE model, results showed that GSK-J4 reduced ISG expression in peritoneal monocytes Arthritis Rheumatol. 2024 Mar;76(3):396-410
Dark Agouti rats Pristane-induced arthritis model Intradermal injection 100 µL Single injection, monitored for 15 weeks To investigate the effect of pre-existing periodontitis on the development and immune/inflammatory response of pristane-induced arthritis. Results showed that pre-existing periodontitis did not affect the development or severity of arthritis. J Transl Med. 2016 Nov 3;14(1):311
Rats Pristane-induced arthritis model Intradermal injection 150 μl Single injection, monitored for 90 days or longer To study the chronic course, histopathological features, and genetic influences of pristane-induced arthritis. Results showed arthritis onset within 2-3 weeks post-injection, characterized by chronic, relapsing, and progressive joint inflammation with bone and cartilage erosions. Am J Pathol. 1996 Nov;149(5):1675-83
Sprague-Dawley rats Pristane-induced arthritis model Intradermal injection 300 µL Administered on day 0 and day 4 To induce arthritis and assess disease severity, results showed successful establishment of pristane-induced arthritis model for evaluating therapeutic effects NPJ Regen Med. 2022 Feb 2;7(1):13
C57BL/6 mice Pristane-induced lupus model Intraperitoneal injection 500 µL Single injection, lasting 8 months To study the impact of cGAS deficiency on lupus pathology. Results showed that Cgas-/- mice exhibited more severe pulmonary hemorrhage, autoantibody production, and inflammatory cell infiltration, indicating cGAS deficiency exacerbates lupus pathology. Front Immunol. 2022 Dec 16;13:1010764
C57BL/6 mice Pristane-induced lupus model Intraperitoneal injection 500 µL Single injection, lasted for 6 months To investigate the effect of iron deficiency on the disease progression of pristane-induced lupus, results showed that iron deficiency improved renal damage, reduced autoantibody production, and promoted Treg cell expansion. Front Immunol. 2022 Feb 28;13:799331
Mice Pristane-induced lupus model Intraperitoneal injection 500 µL Single injection, duration of 6 months To investigate the role of type III interferons in pristane-induced lupus model. Results showed improved survival rates, reduced lipogranuloma formation, and decreased early-phase autoantibody titers in Ifnlr1?/? mice. Int J Mol Sci. 2021 Oct 29;22(21):11747
Mice Systemic lupus erythematosus model Intraperitoneal injection 500 μl Single injection Induction of systemic lupus erythematosus symptoms, including proteinuria, elevated levels of antinuclear antibodies (ANAs) and anti-dsDNA antibodies, and kidney inflammation and immune complex deposition. AIM2 deficiency ameliorated these symptoms. Signal Transduct Target Ther. 2021 Sep 14;6(1):341
Mice Pristane-induced lupus nephritis model Intraperitoneal injection 500 μl Single injection, observation period up to 9 months To evaluate the effect of Pristane on inflammation and immune responses in NLRP12-deficient mice, results showed NLRP12-deficient mice exhibited more severe inflammation and immune responses J Clin Invest. 2023 Feb 1;133(3):e157272
Mice Pristane-induced lupus model Intraperitoneal injection 500 μl Single injection To investigate the role of AIM2 in lupus development, results showed that AIM2 deficiency ameliorated lupus symptoms Clin Transl Med. 2022 Mar;12(3):e781
C57BL/6 mice Pristane-induced lupus nephritis model Intraperitoneal injection 500 μl Single injection, lasting for 4 months To study the Pristane-induced lupus nephritis model for evaluating the therapeutic effect of exosomes derived from BMMSCs on lupus nephritis. Stem Cell Res Ther. 2022 Sep 24;13(1):484
BALB/c mice Pristane-induced lupus nephritis model Intraperitoneal injection 500 μL Single injection To evaluate the effects of Pristane on lupus nephritis, results showed that Pristane-induced LN mice exhibited severe renal damage, including glomerulonephritis and tubular inflammation. Int J Mol Sci. 2019 Jul 15;20(14):3466
Mice Dnase1–/–Dnase1L3–/– double-knockout mice Intraperitoneal injection 500 μL Single dose Accelerated disease phenotype, resulting in 50% mortality in untreated DKO mice, while LBme-treated DKO mice showed reduced mortality to 15% JCI Insight. 2024 Jun 18;9(14):e177003

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.72mL

0.74mL

0.37mL

18.62mL

3.72mL

1.86mL

37.24mL

7.45mL

3.72mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

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