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Merck
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H3648

Sigma-Aldrich

(±)-3-羟基癸酸

≥98%

别名:

DL-β-羟基癸酸

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About This Item

经验公式（希尔记法）:
C10H20O3
CAS号:
5561-87-5
分子量:
188.26
MDL编号:
MFCD00133275
UNSPSC代码:
12352211
PubChem化学物质编号:
24895586
NACRES:
NA.25
价格与库存信息目前不能提供

质量水平

200

方案

≥98%

表单

powder

官能团

carboxylic acid

脂质类型

saturated FAs

运输

ambient

储存温度

2-8°C

SMILES字符串

CCCCCCCC(O)CC(O)=O

InChI

1S/C10H20O3/c1-2-3-4-5-6-7-9(11)8-10(12)13/h9,11H,2-8H2,1H3,(H,12,13)

InChI key

FYSSBMZUBSBFJL-UHFFFAOYSA-N

相关类别

应用


  • LORE受体同源化是3-羟基癸酸诱导的免疫信号转导所必需的，并决定了拟南芥属内免疫敏感性的自然变异。：该研究揭示了3-羟基癸酸通过 LORE 受体同源化在植物中介导免疫反应的关键作用，为植物防御的分子机制和潜在的农业应用提供了启示（Eschrig et al., 2024）。


储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000382652
0000382652
0000298381
0000298383
SLCR5367

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E Déziel et al.
Biochimica et biophysica acta, 1440(2-3), 244-252 (1999-10-16)
Liquid chromatography/mass spectrometry using electrospray ionisation was used to analyse rhamnolipids produced by a Pseudomonas aeruginosa strain with mannitol or naphthalene as carbon source. Identification and quantification of 28 different rhamnolipid congeners was accomplished using a reverse-phase C(18) column and
B Füchtenbusch et al.
Applied microbiology and biotechnology, 53(2), 167-172 (2000-03-10)
Screening experiments identified several bacteria which were able to use residual oil from biotechnological rhamnose production as a carbon source for growth. Ralstonia eutropha H16 and Pseudomonas oleovorans were able to use this waste material as the sole carbon source
Florian Bredenbruch et al.
Journal of bacteriology, 187(11), 3630-3635 (2005-05-20)
The role of intercellular communication in the regulation of bacterial multicellular behavior has received widespread attention, and a variety of signal molecules involved in bacterial communication have been discovered. In addition to the N-acyl-homoserine lactones, 4-hydroxy-2-alkylquinolines (HAQs), including the Pseudomonas
Ahmad Mohammad Abdel-Mawgoud et al.
Applied microbiology and biotechnology, 86(5), 1323-1336 (2010-03-26)
Rhamnolipids are glycolipidic biosurfactants produced by various bacterial species. They were initially found as exoproducts of the opportunistic pathogen Pseudomonas aeruginosa and described as a mixture of four congeners: alpha-L-rhamnopyranosyl-alpha-L-rhamnopyranosyl-beta-hydroxydecanoyl-beta-hydroxydecanoate (Rha-Rha-C(10)-C(10)), alpha-L-rhamnopyranosyl-alpha-L-rhamnopyranosyl-beta-hydroxydecanoate (Rha-Rha-C(10)), as well as their mono-rhamnolipid congeners Rha-C(10)-C(10)
Highly regioselective Vilsmeier-Haack acylation of hexahydropyrroloindolizine.
B Sayah et al.
The Journal of organic chemistry, 66(7), 2522-2525 (2001-04-03)
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