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2,5-二氯苯氧基乙酸 | 582-54-7

中文名称
2,5-二氯苯氧基乙酸
中文别名
乙酸,(2,5-二氯苯氧基)-(8CI)(9CI);(2,5-二氯苄酚氧基)乙酸;2-(2,5-二氯苯氧基)乙酸;2,5-二氯苯氧乙酸;乙酸,(2,5-二氯苯氧基)-
英文名称
2,5-dichlorophenoxyacetic acid
英文别名
(2,5-Dichlor-phenoxy)-essigsaeure;2-(2,5-dichlorophenoxy)acetic acid
2,5-二氯苯氧基乙酸化学式
CAS
582-54-7
化学式
C8H6Cl2O3
mdl
MFCD02127529
分子量
221.04
InChiKey
YVPLLFUCNGVUAY-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

  • 熔点:
    142-143 °C
  • 沸点:
    316.96°C (rough estimate)
  • 密度:
    1.4564 (rough estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2918990090
  • 储存条件:
    室温

SDS

SDS:e1c4ff1dfe4f96e92361909079e28706
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SECTION 1: Identification of the substance/mixture and of the company/undertaking
Product identifiers
Product name : (2,5-Dichlorophenoxy)Acetic Acid
: OTV000322
REACH No. : A registration number is not available for this substance as the substance
or its uses are exempted from registration, the annual tonnage does not
require a registration or the registration is envisaged for a later
registration deadline.


SECTION 2: Hazards identification
Classification of the substance or mixture
Classification according to Regulation (EC) No 1272/2008
Acute toxicity, Oral (Category 4), H302
For the full text of the H-Statements mentioned in this Section, see Section 16.
Classification according to EU Directives 67/548/EEC or 1999/45/EC
Xn Harmful R22
For the full text of the R-phrases mentioned in this Section, see Section 16.
Label elements
Labelling according Regulation (EC) No 1272/2008
Pictogram
Signal word Warning
Hazard statement(s)
Harmful if swallowed.
Precautionary statement(s) none
Supplemental Hazard none
Statements
Other hazards
This substance/mixture contains no components considered to be either persistent, bioaccumulative and
toxic (PBT), or very persistent and very bioaccumulative (vPvB) at levels of 0.1% or higher.

SECTION 3: Composition/information on ingredients
Substances
Molecular weight : 221,04 g/mol
Hazardous ingredients according to Regulation (EC) No 1272/2008
Component Classification Concentration
(2,5-Dichlorophenoxy)Acetic Acid
Acute Tox. 4; H302 <= 100 %
Hazardous ingredients according to Directive 1999/45/EC
Component Classification Concentration
(2,5-Dichlorophenoxy)Acetic Acid
Xn, R22 <= 100 %
For the full text of the H-Statements and R-Phrases mentioned in this Section, see Section 16

SECTION 4: First aid measures
Description of first aid measures
General advice
Consult a physician. Show this safety data sheet to the doctor in attendance.
If inhaled
If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician.
In case of skin contact
Wash off with soap and plenty of water. Consult a physician.
In case of eye contact
Flush eyes with water as a precaution.
If swallowed
Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician.
Most important symptoms and effects, both acute and delayed
The most important known symptoms and effects are described in the labelling (see section 2.2) and/or in
section 11
Indication of any immediate medical attention and special treatment needed
No data available

SECTION 5: Firefighting measures
Extinguishing media
Suitable extinguishing media
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Nature of decomposition products not known.
Advice for firefighters
Wear self-contained breathing apparatus for firefighting if necessary.
Further information
No data available

SECTION 6: Accidental release measures
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment. Avoid dust formation. Avoid breathing vapours, mist or gas. Ensure
adequate ventilation. Avoid breathing dust.
For personal protection see section 8.
Environmental precautions
Do not let product enter drains.
Methods and materials for containment and cleaning up
Pick up and arrange disposal without creating dust. Sweep up and shovel. Keep in suitable, closed
containers for disposal.
Reference to other sections
For disposal see section 13.

SECTION 7: Handling and storage
Precautions for safe handling
Avoid contact with skin and eyes. Avoid formation of dust and aerosols.
Provide appropriate exhaust ventilation at places where dust is formed.
For precautions see section 2.2.
Conditions for safe storage, including any incompatibilities
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
Storage class (TRGS 510): Non Combustible Solids
Specific end use(s)
Apart from the uses mentioned in section 1.2 no other specific uses are stipulated

SECTION 8: Exposure controls/personal protection
Control parameters
Components with workplace control parameters
Exposure controls
Appropriate engineering controls
Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and
at the end of workday.
Personal protective equipment
Eye/face protection
Safety glasses with side-shields conforming to EN166 Use equipment for eye protection tested
and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).
Skin protection
Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique
(without touching glove's outer surface) to avoid skin contact with this product. Dispose of
contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.
The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and
the standard EN 374 derived from it.
Body Protection
Complete suit protecting against chemicals, The type of protective equipment must be selected
according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection
For nuisance exposures use type P95 (US) or type P1 (EU EN 143) particle respirator.For higher
level protection use type OV/AG/P99 (US) or type ABEK-P2 (EU EN 143) respirator cartridges.
Use respirators and components tested and approved under appropriate government standards
such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Do not let product enter drains.

SECTION 9: Physical and chemical properties
Information on basic physical and chemical properties
a) Appearance Form: solid
b) Odour No data available
c) Odour Threshold No data available
d) pH No data available
e) Melting point/freezing No data available
point
f) Initial boiling point and No data available
boiling range
g) Flash point No data available
h) Evaporation rate No data available
i) Flammability (solid, gas) No data available
j) Upper/lower No data available
flammability or
explosive limits
k) Vapour pressure No data available
l) Vapour density No data available
m) Relative density No data available
n) Water solubility No data available
o) Partition coefficient: n- No data available
octanol/water
p) Auto-ignition No data available
temperature
q) Decomposition No data available
temperature
r) Viscosity No data available
s) Explosive properties No data available
t) Oxidizing properties No data available
Other safety information
No data available

SECTION 10: Stability and reactivity
Reactivity
No data available
Chemical stability
Stable under recommended storage conditions.
Possibility of hazardous reactions
No data available
Conditions to avoid
No data available
Incompatible materials
No data available
Hazardous decomposition products
In the event of fire: see section 5

SECTION 11: Toxicological information
Information on toxicological effects
Acute toxicity
No data available
Skin corrosion/irritation
No data available
Serious eye damage/eye irritation
No data available
Respiratory or skin sensitisation
No data available
Germ cell mutagenicity
No data available
Carcinogenicity
IARC: No component of this product present at levels greater than or equal to 0.1% is identified as
probable, possible or confirmed human carcinogen by IARC.
Reproductive toxicity
No data available
Specific target organ toxicity - single exposure
No data available
Specific target organ toxicity - repeated exposure
No data available
Aspiration hazard
No data available
Additional Information
RTECS: Not available

SECTION 12: Ecological information
Toxicity
No data available
Persistence and degradability
No data available
Bioaccumulative potential
No data available
Mobility in soil
No data available
Results of PBT and vPvB assessment
This substance/mixture contains no components considered to be either persistent, bioaccumulative and
toxic (PBT), or very persistent and very bioaccumulative (vPvB) at levels of 0.1% or higher.
Other adverse effects
No data available

SECTION 13: Disposal considerations
Waste treatment methods
Product
Offer surplus and non-recyclable solutions to a licensed disposal company. Dissolve or mix the material
with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber.
Contaminated packaging
Dispose of as unused product.

SECTION 14: Transport information
UN number
ADR/RID: - IMDG: - IATA: -
UN proper shipping name
ADR/RID: Not dangerous goods
IMDG: Not dangerous goods
IATA: Not dangerous goods
Transport hazard class(es)
ADR/RID: - IMDG: - IATA: -
Packaging group
ADR/RID: - IMDG: - IATA: -
Environmental hazards
ADR/RID: no IMDG Marine pollutant: no IATA: no
Special precautions for user
No data available

SECTION 15: Regulatory information
This safety datasheet complies with the requirements of Regulation (EC) No. 1907/2006.
Safety, health and environmental regulations/legislation specific for the substance or mixture
No data available
Chemical Safety Assessment


SECTION 16 - ADDITIONAL INFORMATION
N/A

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:
    参考文献:
    名称:
    Eckstein, Roczniki Chemii, 1956, vol. 30, p. 633
    摘要:
    DOI:
  • 作为产物:
    描述:
    2,5-二氯苯酚potassium carbonate 、 lithium hydroxide 作用下, 以 甲醇N,N-二甲基甲酰胺 为溶剂, 反应 25.0h, 生成 2,5-二氯苯氧基乙酸
    参考文献:
    名称:
    新型除草剂4-羟基-3-(2-苯氧基乙酰基)-吡喃-2-酮衍生物的设计,合成及作用方式评价
    摘要:
    为了开发含有β-三酮基序的新型除草剂,设计并合成了一系列4-羟基-3-(2-苯氧基乙酰基)-吡喃-2-酮衍生物。生物测定结果表明,即使剂量为187.5 g ha –1,化合物II15也具有良好的芽前除草活性。此外,与商业除草剂2,4-二氯苯氧基乙酸(2,4-D)相比,化合物II15的杂草控制范围更广,并且对小麦和玉米具有良好的农作物安全性。当以375 g ha –1施用时在出苗前的条件下,表明其作为除草剂的巨大潜力。更重要的是,研究化合物II15的分子作用方式表明,新的三酮结构是其相应的苯氧乙酸生长素除草剂的除草剂,其除草机理与2,4-D相似。目前的工作表明4-羟基-3-(2-苯氧基乙酰基)-吡喃-2-酮基序可能是潜在的铅结构,用于进一步开发新型的生长素型除草剂。
    DOI:
    10.1021/acs.jafc.9b03109
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文献信息

  • Site-Selective Acceptorless Dehydrogenation of Aliphatics Enabled by Organophotoredox/Cobalt Dual Catalysis
    作者:Min-Jie Zhou、Lei Zhang、Guixia Liu、Chen Xu、Zheng Huang
    DOI:10.1021/jacs.1c05479
    日期:2021.10.13
    cobaloxime to produce olefins and H2. This operationally simple method enables direct dehydrogenation of readily available chemical feedstocks to diversely functionalized olefins. For example, we demonstrate, for the first time, the oxidant-free desaturation of thioethers and amides to alkenyl sulfides and enamides, respectively. Moreover, the system’s exceptional site selectivity and functional group
    脂肪族催化脱氢 (CDA) 在有机合成中的价值在很大程度上仍未得到充分探索。已知的均相 CDA 系统通常需要使用牺牲氢受体(或氧化剂)、贵金属催化剂和苛刻的反应条件,因此将大多数现有方法限制为非或低官能化烷烃的脱氢。在这里,我们描述了一种可见光驱动的双催化剂系统,该系统由廉价的有机光氧化还原和贱金属催化剂组成,用于室温、无受体 CDA (Al-CDA)。该过程由光激发的 2-氯蒽醌引发,涉及脂肪族的 H 原子转移 (HAT) 形成烷基自由基,然后与钴肟反应生成烯烃和 H 2. 这种操作简单的方法能够将容易获得的化学原料直接脱氢成多种官能化的烯烃。例如,我们首次证明了硫醚和酰胺在无氧化剂条件下分别脱饱和为烯基硫醚和烯酰胺。此外,14 种生物相关分子和药物成分的后期脱氢和合成说明了该系统卓越的位点选择性和官能团耐受性。机理研究揭示了双重 HAT 过程,并提供了对反应性和位点选择性起源的见解。
  • [EN] NON-SYSTEMIC TGR5 AGONISTS<br/>[FR] AGONISTES DE TGR5 NON SYSTÉMIQUES
    申请人:ARDELYX INC
    公开号:WO2013096771A1
    公开(公告)日:2013-06-27
    Compounds of structure (I), or a stereoisomer, tautomer, pharmaceutically acceptable salt or prodrug thereof, wherein R1, R2, R3, R4, R8, R9, R10, R11, R12, A1, A2, X, Y and Z are as defined herein. Uses of such compounds as TGR5 antagonists and for treatment of various indications, including Type II diabetes meletus are also provided.
    结构(I)的化合物,或其立体异构体、互变异构体、药学上可接受的盐或前药,其中R1、R2、R3、R4、R8、R9、R10、R11、R12、A1、A2、X、Y和Z如本文所定义。提供了这些化合物作为TGR5拮抗剂的用途,以及用于治疗各种适应症,包括II型糖尿病。
  • Discovery, synthesis and biological characterization of a series of <i>N</i>-(1-(1,1-dioxidotetrahydrothiophen-3-yl)-3-methyl-1<i>H</i>-pyrazol-5-yl)acetamide ethers as novel GIRK1/2 potassium channel activators
    作者:Swagat Sharma、Lauren Lesiak、Christopher D. Aretz、Yu Du、Sushil Kumar、Nagsen Gautam、Yazen Alnouti、Nikilesh V. Dhuria、Yashpal S. Chhonker、C. David Weaver、Corey R. Hopkins
    DOI:10.1039/d1md00129a
    日期:——
    The present study describes the discovery and characterization of a series of N-(1-(1,1-dioxidotetrahydrothiophen-3-yl)-3-methyl-1H-pyrazol-5-yl)acetamide ethers as G protein-gated inwardly-rectifying potassium (GIRK) channel activators. From our previous lead optimization efforts, we have identified a new ether-based scaffold and paired this with a novel sulfone-based head group to identify a potent
    本研究描述了一系列N -(1-(1,1-二氧化四氢噻吩-3-基)-3-甲基-1 H-吡唑-5-基)乙酰胺醚作为 G 蛋白内门控的发现和表征-整流钾(GIRK)通道激活剂。从我们之前的先导化合物优化工作中,我们已经确定了一种新的基于醚的支架,并将其与一种新型的基于砜的头基配对,以确定一种有效且选择性的 GIRK1/2 激活剂。此外,我们在第 1 层 DMPK 测定中评估了这些化合物,并确定了作为 GIRK1/2 激活剂显示纳摩尔效力的化合物,与典型的基于尿素的化合物相比,其代谢稳定性得到了改善。
  • An Efficient One-Pot Synthesis of 2-(Aryloxyacetyl)cyclohexane-1,3-diones as Herbicidal 4-Hydroxyphenylpyruvate Dioxygenase Inhibitors
    作者:Da-Wei Wang、Hong-Yan Lin、Bo He、Feng-Xu Wu、Tao Chen、Qiong Chen、Wen-Chao Yang、Guang-Fu Yang
    DOI:10.1021/acs.jafc.6b04110
    日期:2016.11.30
    4-Hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27, HPPD) is an important target for new bleaching herbicides discovery. As a continuous work to discover novel crop selective HPPD inhibitor, a series of 2-(aryloxyacetyl)cyclohexane-1,3-diones were rationally designed and synthesized by an efficient one-pot procedure using N,N′-carbonyldiimidazole (CDI), triethylamine, and acetone cyanohydrin in CH2Cl2
    4-羟基苯基丙酮酸双加氧酶(EC 1.13.11.27,HPPD)是发现新的漂白除草剂的重要目标。为发现新型农作物选择性HPPD抑制剂而进行的持续工作,使用N,N'-羰基二咪唑(CDI),通过高效的一锅法合理设计和合成了一系列2-(芳氧基乙酰基)环己烷-1,3-二酮,三乙胺和丙酮氰醇在CH 2 Cl 2中。总共以良好至优异的产率合成了58种三酮化合物。一些三酮类化合物显示出有效的体外拟南芥HPPD(At HPPD)抑制活性。2-(2-(((1-溴萘-2-基)氧基)乙酰基)-3-羟基环己基-2-烯-1-酮,II-13,在37.5–150 g ai / ha的剂量下表现出高,广谱和芽后除草活性,几乎与甲基磺草酮对某些杂草一样有效。此外,II-13在150 g ai / ha的速率下对玉米和低芥酸菜籽显示出良好的农作物安全性,这表明II-13可能作为除草剂用于控制玉米和低芥酸菜子田中的杂草。II
  • Effective catalytic hydrodechlorination of chlorophenoxyacetic acids over Pd/graphitic carbon nitride
    作者:Fang Jiang、Wenhui Tan、Huan Chen、Ling Tan、Jingliang Liu
    DOI:10.1039/c5ra07913f
    日期:——

    Catalytic hydrodechlorination (HDC) of chlorophenoxyacetic acids was performed over Pd/graphitic carbon nitride (Pd/g-C3N4) catalysts in the present work.

    在本研究中,对氯苯氧乙酸进行了在Pd/石墨碳硝化物(Pd/g-C3N4)催化剂上的催化脱氯(HDC)反应。
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(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐