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重要文件

LM2511

Avanti

Glucosyl (β) C12 Ceramide

Avanti Research - A Croda Brand LM2511, ethanol solution

同義詞:

N-(dodecanoyl)-1-β-glucosyl-sphing-4-ene

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About This Item

經驗公式(希爾表示法):
C36H69NO8
CAS號碼:
分子量::
643.93
分類程式碼代碼:
12352211
NACRES:
NA.25

形狀

ethanol solution

包裝

pkg of 1 × 1 mL (LM2511-1EA)

製造商/商標名

Avanti Research - A Croda Brand LM2511

濃度

~10 μg/mL (Refer to C of A for lot specific concentration.)

應用

lipidomics
metabolomics

運輸包裝

dry ice

儲存溫度

−20°C

SMILES 字串

[H][C@](/C=C/CCCCCCCCCCCCC)(O)[C@@]([H])(NC(CCCCCCCCCCC)=O)CO[C@H](O1)[C@H](O)[C@@H](O)[C@@H]([C@H]1CO)O

InChI

1S/C36H69NO8/c1-3-5-7-9-11-13-14-15-16-18-19-21-23-25-30(39)29(28-44-36-35(43)34(42)33(41)31(27-38)45-36)37-32(40)26-24-22-20-17-12-10-8-6-4-2/h23,25,29-31,33-36,38-39,41-43H,3-22,24,26-28H2,1-2H3,(H,37,40)/b25-23+/t29-,30+,31?,33+,34?,35?,36+/m0/s1

InChI 密鑰

IYCYEZLMOLRFAN-QGJHTTTBSA-N

應用

Lactosyl (β) C12 Ceramide is suitable as an internal standard:
  • to determine if the isopropanol is a choice procedure for large-scale lipid profiling using UHPLC-MS
  • to assess the effects of diabetes and the treatment with dihydroprogesterone (DHP) in rat cerebral cortex
  • in the lipidomic analysis of extracellular vesicles (EVs) released by human fibroblasts undergoing Oncogene-Induced Senescence (OIS)

包裝

2 mL Amber Glass Sealed Ampule (LM2511-1EA)

法律資訊

Avanti Research is a trademark of Avanti Polar Lipids, LLC

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象形圖

FlameExclamation mark

訊號詞

Danger

危險聲明

危險分類

Eye Irrit. 2 - Flam. Liq. 2

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

55.4 °F - closed cup

閃點(°C)

13.0 °C - closed cup


從最近期的版本中選擇一個:

分析證明 (COA)

Lot/Batch Number

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存取文件庫

Isopropanol extraction for cerebrospinal fluid lipidomic profiling analysis
Iriondo A, et al.
Talanta, 195, 619-627 (2019)
Extracellular vesicles released by fibroblasts undergoing H-Ras induced senescence show changes in lipid profile
Buratta S, et al.
PLoS ONE, 12(11), e0188840-e0188840 (2017)
Diabetes alters myelin lipid profile in rat cerebral cortex: Protective effects of dihydroprogesterone
Cermenati G, et al.
The Journal of Steroid Biochemistry and Molecular Biology, 168, 60-70 (2017)

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