摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(10Z,12Z)-10,12-Octadecadienoic acid | 7307-45-1

中文名称
——
中文别名
——
英文名称
(10Z,12Z)-10,12-Octadecadienoic acid
英文别名
(10Z,12Z)-Octadeca-9,11-dienoic acid;cis-10,cis-12-octadecadienoic acid;c10,c12-Conjugated linoleic acid;octadeca-10Z,12Z-dienoic acid;cis-10,12-linoleic acid;10c, 12c-linoleic acid;10Z,12Z-octadecadienoic acid;(10Z,12Z)-octadeca-10,12-dienoic acid
(10Z,12Z)-10,12-Octadecadienoic acid化学式
CAS
7307-45-1
化学式
C18H32O2
mdl
——
分子量
280.451
InChiKey
GKJZMAHZJGSBKD-JPDBVBESSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    38.2-39.0 °C
  • 沸点:
    377.7±11.0 °C(Predicted)
  • 密度:
    0.8810 g/cm3(Temp: 70 °C)

计算性质

  • 辛醇/水分配系数(LogP):
    7.1
  • 重原子数:
    20
  • 可旋转键数:
    14
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.72
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

SDS

SDS:c7b3d7ca412f0095eb6ef51fa805b403
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Compositions comprising reverse isomers of conjugated linoleic acid
    申请人:Saebo Asgeir
    公开号:US20050215641A1
    公开(公告)日:2005-09-29
    The present invention relates to the field of human and animal nutrition, and in particular to certain novel compositions of conjugated linoleic acids (CLA). In particular, the present invention relates to CLA compositions comprising the c10,t12, c10,c12, t9,c11 and c9,c11 isomers of conjugated linoleic acid.
    本发明涉及人类和动物营养领域,特别是某些新颖的共轭亚油酸(CLA)组合物。具体而言,本发明涉及包含共轭亚油酸的c10,t12、c10,c12、t9,c11和c9,c11异构体的CLA组合物。
  • Process
    申请人:Yan Youchan
    公开号:US20050124818A1
    公开(公告)日:2005-06-09
    A process for producing a conjugated di- or poly-unsaturated fatty acid having from 12 to 24 carbon atoms, or a salt or ester thereof, comprises reacting a non-conjugated free fatty acid, or a salt or ester thereof with a base in the presence of a solvent comprising a monohydric alcohol having from 1 to 6 carbon atoms, wherein the reaction is carried out at a temperature of from 120° C. to 200° C. in the presence of water in an amount of at least 4% by weight based on alcohol.
    生产具有12到24个碳原子的共轭二元或多元不饱和脂肪酸,或其盐或酯的方法包括在溶剂中与一种具有1到6个碳原子的一元醇反应,其中所述反应在温度为120°C至200°C的条件下进行,在水的存在下,水的含量至少为醇的重量的4%。
  • Compounds that modulate fatty acid receptor activity and pet food products containing the same
    申请人:MARS, INCORPORATED
    公开号:US10827772B2
    公开(公告)日:2020-11-10
    A flavor composition comprising at least one compound that modulates, increases and/or enhances the activity of a GPR120 fatty acid receptor that can be used to enhance the fatty acid taste and/or palatability of pet food products is described herein. Also disclosed herein are methods for identifying said compounds.
    本文描述了一种风味组合物,该组合物包含至少一种可调节、增加和/或增强 GPR120 脂肪酸受体活性的化合物,可用于增强宠物食品的脂肪酸味道和/或适口性。本文还公开了鉴定所述化合物的方法。
  • Methods and compositions for treating diabetes
    申请人:Vanden Heuvel P. John
    公开号:US20050282897A1
    公开(公告)日:2005-12-22
    Methods of treating diabetes in an animal and food compositions useful for treating diabetes are described. In one aspect of the invention, the method includes treating the animal with a therapeutically effective amount of CLA including 9,11-octadecadienoic acid and 10,12-octadecadienoic acid, isomers thereof, esters thereof, salts thereof or mixtures thereof. In another aspect of the invention, a food composition comprising a food product having a therapeutically effective amount of a purified CLA isomer, including cis,cis-9,11-octadecadienoic acid, trans,cis-10,12-octadecadienoic acid or a mixture of purified cis,trans-9,11-ocatadecadienoic acid and trans,cis-0,11-octadecadienoic acid is described.
    本发明描述了治疗动物糖尿病的方法和用于治疗糖尿病的食品组合物。在本发明的一个方面,该方法包括用治疗有效量的 CLA(包括 9,11-十八碳二烯酸和 10,12-十八碳二烯酸)、其异构体、其酯、其盐或其混合物治疗动物。在本发明的另一方面,描述了一种食品组合物,该组合物包含具有治疗有效量的纯化CLA异构体的食品,包括顺式、顺式-9,11-十八碳二烯酸、反式、顺式-10,12-十八碳二烯酸或纯化的顺式、反式-9,11-十八碳二烯酸和反式、顺式-0,11-十八碳二烯酸的混合物。
  • A simple method of preparation of methyl<i>trans</i>-10,<i>cis</i>-12- and<i>cis</i>-9,<i>trans</i>-11-octadecadienoates from methyl linoleate
    作者:O. Berdeaux、L. Voinot、E. Angioni、P. Juanéda、J. L. Sébédio
    DOI:10.1007/s11746-998-0327-x
    日期:1998.12
    AbstractPure conjugated isomers of linoleic acid were prepared on a large scale by alkali‐isomerization of purified methyl linoleate. The methyl esters of alkali‐isomerized linoleic acid contained mainly the methyl cis‐9,trans‐11‐ and trans‐10,cis‐12‐octadecadienoates (44 and 47%, respectively). These two isomers were then separated and purified by a series of low‐temperature crystallizations from acetone. The isomeric purity obtained for the cis‐9,trans‐11‐octadecadienoate isomer was >90% and that of the trans‐10,cis‐12‐octadecadienoate isomer was 89 to 97%. The isolated yield of the two isomers corresponded to 18 and 25.7%, respectively, of the starting material. The structure of the two isomers was confirmed using partial hydrazine reduction, silver nitrate‐thin‐layer chromatography of the resulting monoenes and gas chromatography coupled with mass spectrometry of the 4,4‐dimethyloxazoline derivatives. Fourier transform infrared spectroscopy of the monoenes gave the confirmation of the geometry of each double bond.
查看更多