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六乙二醇单甲醚 | 23601-40-3

中文名称
六乙二醇单甲醚
中文别名
六乙二醇甲醚;六乙二醇一甲醚
英文名称
hexaethylene glycol monomethyl ether
英文别名
2,5,8,11,14,17-hexaoxanonadecan-19-ol;2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethanol
六乙二醇单甲醚化学式
CAS
23601-40-3
化学式
C13H28O7
mdl
MFCD00045996
分子量
296.361
InChiKey
FHHGCKHKTAJLOM-UHFFFAOYSA-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

  • 沸点:
    167 °C / 1mmHg
  • 密度:
    1,08 g/cm3
  • 保留指数:
    2069.1;2056

计算性质

  • 辛醇/水分配系数(LogP):
    -1.3
  • 重原子数:
    20
  • 可旋转键数:
    17
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    75.6
  • 氢给体数:
    1
  • 氢受体数:
    7

安全信息

  • 海关编码:
    2909499000
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H315,H319,H335
  • 储存条件:
    存放于室温、干燥且密封的环境中。

SDS

SDS:71b134ca1eee5bdb42fd74f511675f73
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Hexaethylene Glycol Monomethyl Ether Revision number: 5
SAFETY DATA SHEET

Section 1. IDENTIFICATION
Product name: Hexaethylene Glycol Monomethyl Ether

Revision number: 5

Section 2. HAZARDS IDENTIFICATION
GHS classification
PHYSICAL HAZARDS Not classified
Not classified
HEALTH HAZARDS
ENVIRONMENTAL HAZARDS Not classified
GHS label elements, including precautionary statements
Pictograms or hazard symbols None
No signal word
Signal word
Hazard statements None
None
Precautionary statements:

Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Substance/mixture: Substance
Components: Hexaethylene Glycol Monomethyl Ether
Percent: >96.0%(GC)
CAS Number: 23601-40-3
Chemical Formula: C13H28O7

Section 4. FIRST AID MEASURES
Inhalation: Remove victim to fresh air and keep at rest in a position comfortable for breathing.
Get medical advice/attention if you feel unwell.
Skin contact: Remove/Take off immediately all contaminated clothing. Rinse skin with
water/shower. If skin irritation or rash occurs: Get medical advice/attention.
Eye contact: Rinse cautiously with water for several minutes. Remove contact lenses, if present
and easy to do. Continue rinsing. If eye irritation persists: Get medical
advice/attention.
Ingestion: Get medical advice/attention if you feel unwell. Rinse mouth.
A rescuer should wear personal protective equipment, such as rubber gloves and air-
Protection of first-aiders:
tight goggles.

Section 5. FIRE-FIGHTING MEASURES
Suitable extinguishing Dry chemical, foam, water spray, carbon dioxide.
media:
Unsuitable extinguishing Solid streams of water
media:
Hexaethylene Glycol Monomethyl Ether

Section 5. FIRE-FIGHTING MEASURES
Precautions for firefighters: Fire-extinguishing work is done from the windward and the suitable fire-extinguishing
method according to the surrounding situation is used. Uninvolved persons should
evacuate to a safe place. In case of fire in the surroundings: Remove movable
containers if safe to do so.
Special protective When extinguishing fire, be sure to wear personal protective equipment.
equipment for firefighters:

Section 6. ACCIDENTAL RELEASE MEASURES
Use personal protective equipment. Keep people away from and upwind of spill/leak.
Personal precautions,
protective equipment and Ensure adequate ventilation. Entry to non-involved personnel should be controlled
emergency procedures: around the leakage area by roping off, etc.
Environmental precautions: Prevent product from entering drains.
Methods and materials for Absorb spilled material in a suitable absorbent (e.g. rag, dry sand, earth, saw-dust).
containment and cleaning In case of large amount of spillage, contain a spill by bunding. Adhered or collected
up: material should be promptly disposed of, in accordance with appropriate laws and
regulations.

Section 7. HANDLING AND STORAGE
Precautions for safe handling
Technical measures: Handling is performed in a well ventilated place. Wear suitable protective equipment.
Prevent generation of vapour or mist. Wash hands and face thoroughly after
handling.
Use a ventilation, local exhaust if vapour or aerosol will be generated.
Advice on safe handling: Avoid contact with skin, eyes and clothing.
Conditions for safe storage, including any
incompatibilities
Storage conditions: Keep container tightly closed. Store in a cool and dark place.
Store under inert gas.
Protect from moisture.
Store away from incompatible materials such as oxidizing agents.
Hygroscopic
Packaging material: Comply with laws.

Section 8. EXPOSURE CONTROLS / PERSONAL PROTECTION
Engineering controls: Install a closed system or local exhaust as possible so that workers should not be
exposed directly. Also install safety shower and eye bath.
Personal protective equipment
Respiratory protection: Vapor respirator. Follow local and national regulations.
Hand protection: Protective gloves.
Safety glasses. A face-shield, if the situation requires.
Eye protection:
Skin and body protection: Protective clothing. Protective boots, if the situation requires.

Section 9. PHYSICAL AND CHEMICAL PROPERTIES
Physical state (20°C): Liquid
Clear
Form:
Colour: Colorless - Pale yellow
No data available
Odour:
pH: No data available
Melting point/freezing point:No data available
Boiling point/range: 167°C/0.1kPa
No data available
Flash point:
Flammability or explosive
limits:
Lower: No data available
Upper: No data available
Relative density: 1.08
Hexaethylene Glycol Monomethyl Ether

Section 9. PHYSICAL AND CHEMICAL PROPERTIES
Solubility(ies):
No data available
[Water]
[Other solvents] No data available

Section 10. STABILITY AND REACTIVITY
Chemical stability: Stable under proper conditions.
Possibility of hazardous No special reactivity has been reported.
reactions:
Incompatible materials: Oxidizing agents
Hazardous decomposition Carbon monoxide, Carbon dioxide
products:

Section 11. TOXICOLOGICAL INFORMATION
Acute Toxicity: No data available
Skin corrosion/irritation: No data available
Serious eye No data available
damage/irritation:
Germ cell mutagenicity: No data available
Carcinogenicity:
IARC = No data available
No data available
NTP =
Reproductive toxicity: No data available

Section 12. ECOLOGICAL INFORMATION
Ecotoxicity:
Fish: No data available
Crustacea: No data available
Algae: No data available
Persistence / degradability: No data available
Bioaccumulative No data available
potential(BCF):
Mobility in soil
Log Pow: No data available
Soil adsorption (Koc): No data available
Henry's Law No data available
constant(PaM3/mol):

Section 13. DISPOSAL CONSIDERATIONS
Recycle to process, if possible. Consult your local regional authorities. You may be able to burn in a chemical
incinerator equipped with an afterburner and scrubber system. Observe all federal, state and local regulations when
disposing of the substance.

Section 14. TRANSPORT INFORMATION
Hazards Class: Does not correspond to the classification standard of the United Nations
UN-No: Not listed

Section 15. REGULATORY INFORMATION
Safe management ordinance of dangerous chemical product (State Council announces on January 26, 2002
and revised on February 16,2011): Safe use and production, the storage of a dangerous chemical, transport,
loading and unloading were prescribed.
Hexaethylene Glycol Monomethyl Ether


SECTION 16 - ADDITIONAL INFORMATION
N/A

制备方法与用途

六亚甲基甘醇单甲醚是一种PROTAC连接子,属于PEG类化合物,可用来合成PROTAC分子。

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    六乙二醇单甲醚吡啶4-二甲氨基吡啶 、 sodium azide 、 三苯基膦 作用下, 以 四氢呋喃二氯甲烷丙酮 为溶剂, 反应 11.25h, 生成 3,6,9,12-四氧杂十三胺
    参考文献:
    名称:
    N-Monosubstituted Methoxy-oligo(ethylene glycol) Carbamate Ester Prodrugs of Resveratrol
    摘要:
    白藜芦醇是一种具有多种有趣生物活性的天然多酚。然而,它在体内的药理利用受到其在肠道和肝脏(最重要的是)通过II相共轭代谢迅速消除的阻碍。一种绕过这一问题的方法依赖于前药。我们在这里报告了白藜芦醇前药的合成、表征、水解和体内药代动力学行为,其中OH基团参与了N-单取代氨基甲酸酯酯键。作为载体,使用了一系列定义链长(n=3、4、6)的甲氧基聚乙二醇(m-OEG)(CH3–[OCH2CH2]n–)。这些有望像较长的聚乙二醇(PEG)链一样,调节所得到的衍生物的化学物理性质,同时保留相对较低的分子量,从而具有良好的药物负载能力。对大鼠进行胃内给药,结果表明,血液中出现了前药及其部分水解产物,证实了在吸收过程中避免了首次通过代谢的保护。
    DOI:
    10.3390/molecules200916085
  • 作为产物:
    描述:
    二乙二醇单甲醚potassium tert-butylate三乙胺 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 20.0h, 生成 六乙二醇单甲醚
    参考文献:
    名称:
    Alkaline earth metal-sensing anthracene fluorophore-hosts
    摘要:
    合成了新型的蒽荧光探针-宿主1–4,通过酯或醚键连接到冠醚或聚醚侧臂。向宿主溶液中添加碱土金属阳离子会引起独特的荧光强度变化。具体而言,通过酯键连接的宿主(化合物1和3)会导致荧光淬灭,而通过醚键连接的宿主(化合物2和4)则会导致荧光增强。具有冠醚侧臂的宿主(化合物2)对钙阳离子的识别能力强于对钡阳离子的识别能力;相反,具有聚醚侧臂的宿主(化合物4)则更倾向于识别钡阳离子而非钙阳离子。
    DOI:
    10.1039/a607688b
  • 作为试剂:
    描述:
    3-甲基巴豆酰氯potassium thioacyanate六乙二醇单甲醚 作用下, 以 二氯甲烷 为溶剂, 反应 4.0h, 以70.2%的产率得到3-methyl-but-2-enoyl isothiocyanate
    参考文献:
    名称:
    [EN] TRIAZOLO COMPOUNDS AS PDE10 INHIBITORS
    [FR] COMPOSÉS TRIAZOLO EN TANT QU'INHIBITEURS DE PDE10
    摘要:
    本发明提供了式(Ia)和(Ib)的化合物,其中R1、R2、R3和R4如说明书和权利要求中所定义,以及其生理上可接受的盐。这些化合物抑制PDE10A,可用作药物。
    公开号:
    WO2013178572A1
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文献信息

  • [EN] A CONJUGATE OF A TUBULYSIN ANALOG WITH BRANCHED LINKERS<br/>[FR] CONJUGUÉ D'UN ANALOGUE DE TUBULYSINE AVEC DES LIEURS RAMIFIÉS
    申请人:HANGZHOU DAC BIOTECH CO LTD
    公开号:WO2019127607A1
    公开(公告)日:2019-07-04
    The present invention relates to the conjugation of a tubulysin analog compound to a cell-binding molecule with branched/side-chain linkers for having better delivery of the conjugate compound and targeted treatment of abnormal cells. It also relates to a branched-linkage method of conjugation of a tubulysin analog molecule to a cell-binding ligand, as well as methods of using the conjugate in targeted treatment of cancer, infection and autoimmune disease.
    本发明涉及将一种管腔霉素类似物化合物与具有分支/侧链连接物的细胞结合分子结合,以实现结合物的更好传递和靶向治疗异常细胞。它还涉及一种将管腔霉素类似物分子与细胞结合配体结合的分支连接方法,以及在靶向治疗癌症、感染和自身免疫疾病中使用结合物的方法。
  • Bna Conjugates and Methods of Use
    申请人:James Kenneth D.
    公开号:US20080207505A1
    公开(公告)日:2008-08-28
    Modified natriuretic compounds and conjugates thereof are disclosed in the present invention. In particular, conjugated forms of hBNP are provided that include at least one modifying moiety attached thereto. The modified natriuretic compound conjugates retain activity for stimulating cGMP production, binding to NPR-A receptor, decreasing arterial blood pressure and in some embodiments an improved half-life in circulation as compared to unmodified counterpart natriuretic compounds. Oral, parenteral, enteral, subcutaneous, pulmonary, and intravenous forms of the compounds and conjugates may be prepared as treatments and/or therapies for heart conditions particularly congestive heart failure. Modifying moieties comprising oligomeric structures having a variety of lengths and configurations are also disclosed. Analogs of the hBNP compound are also disclosed, having an amino acid sequence that is other than the native sequence.
    本发明公开了改性利钠肽化合物及其共轭物。具体而言,提供了至少连接有一个修饰基团的hBNP的共轭形式。这些改性利钠肽化合物共轭物保留了刺激cGMP产生、结合NPR-A受体、降低动脉血压以及在某些实施例中相对于未经改性的对应利钠肽化合物具有改善的循环半衰期的活性。这些化合物和共轭物的口服、静脉注射、肠内、皮下、肺部和静脉形式可作为治疗和/或治疗心脏病症,特别是充血性心力衰竭的治疗。还公开了包含具有各种长度和构型的寡聚结构的修饰基团。此外,还公开了hBNP化合物的类似物,其氨基酸序列与天然序列不同。
  • Designer Nanorings with Functional Cavities from Self-Assembling β-Sheet Peptides
    作者:Il-Soo Park、You-Rim Yoon、Minseon Jung、Kimoon Kim、SeongByeong Park、Seokmin Shin、Yong-beom Lim、Myongsoo Lee
    DOI:10.1002/asia.201000428
    日期:2011.2.1
    artificial β‐barrel proteins at will. Here, we describe a rational approach to construct β‐barrel protein mimics from the self‐assembly of peptide‐based building blocks. With this approach, the direction of the self‐assembly process toward the formation of water‐soluble β‐barrel nanorings or water‐insoluble transmembrane β‐barrel pores could be controlled by the simple but versatile molecular manipulation
    呈环状的β-桶蛋白在许多类型的水溶性酶和水不溶性跨膜成孔蛋白中很常见。由于β-桶形蛋白质在细胞中具有多种功能,因此,如果我们能够随意控制人工β-桶形蛋白质的极性,这将是开发人工蛋白质的重要​​一步。在这里,我们描述了一种从基于肽的构件的自组装构建β-桶状蛋白模拟物的合理方法。通过这种方法,可以通过对超分子构件的简单而通用的分子操作来控制自组装过程向水溶性β-桶纳米环或水不溶性跨膜β-桶孔形成的方向。
  • Self-Assembly of Photochromic Diarylethenes with Amphiphilic Side Chains:  Reversible Thermal and Photochemical Control
    作者:Takashi Hirose、Kenji Matsuda、Masahiro Irie
    DOI:10.1021/jo060505t
    日期:2006.9.1
    Diarylethene derivatives with hexaethylene glycol side chains were synthesized and their self-assembling and photochromic reactivity were investigated. The diarylethenes showed photochromism in organic solvents and even in water. The aqueous solution of the compounds turned turbid quickly upon heating. The clouding behavior was investigated using 1H NMR spectroscopy, dynamic light scattering, and absorption
    合成了具有六甘醇侧链的二芳基乙烯衍生物,并研究了它们的自组装和光致变色反应性。二芳烃在有机溶剂甚至水中显示出光致变色现象。化合物的水溶液在加热后迅速变浑浊。使用1调查了混浊行为1 H NMR光谱,动态光散射和吸收光谱。发现在水溶液中,化合物自组装成聚集体,并且通过升高温度使聚集体疏松。闭环异构体的浊点温度比开环异构体的浊点温度低5-7°C。当在两亲性侧链中引入不对称甲基时,在水中用紫外线照射时会观察到诱导的圆二色性(ICD)。该ICD是通过开环和闭环异构体之间自组装行为的差异来解释的。建议闭环异构体组装成手性纳米结构。
  • Pharmaceutical compositions of drug-oligomer conjugates and methods of treating diseases therewith
    申请人:——
    公开号:US20030069170A1
    公开(公告)日:2003-04-10
    Pharmaceutical compositions that include a drug-oligomer conjugate, a fatty acid component, and a bile salt component are described. The drug is covalently coupled to an oligomeric moiety. The fatty acid component and the bile salt component are present in a weight-to-weight ratio of between 1:5 and 5:1. Methods of treating diseases in a subject in need of such treatment using such pharmaceutical compositions are also provided, as are methods of providing such pharmaceutical compositions.
    描述了包括药物-寡聚物共轭物、脂肪酸成分和胆盐成分的药物组合物。药物以共价键连接到寡聚物基团上。脂肪酸成分和胆盐成分以1:5至5:1的重量比存在。还提供了利用这种药物组合物治疗需要此类治疗的受试者的方法,以及提供这种药物组合物的方法。
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