全氟辛酰氯 | 335-64-8

• 物质功能分类: 有机原料 - 羧酸类化合物及衍生物 - 羧酸酰卤化物
• 分子结构分类: 有机化合物 - 有机卤素化合物 - 酰卤
• 中文名称: 全氟辛酰氯
• 中文别名: 十五氟辛酰氯
• 英文名称: pentadecafluorooctanoyl chloride
• 英文别名: Perfluorooctanoyl chloride；2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanoyl chloride
• CAS: 335-64-8
• 化学式: C₈ClF₁₅O
• mdl: MFCD00013654
• 分子量: 432.516
• InChiKey: AQQBRCXWZZAFOK-UHFFFAOYSA-N

物化性质

• 熔点：
  74-75 °C(Solv: benzene (71-43-2))
• 沸点：
  129-130 °C/744 mmHg (lit.)
• 密度：
  1.744 g/mL at 25 °C (lit.)
• 闪点：
  >230 °F

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  25
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.875
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  16

安全信息

• 危险等级：
  8
• 危险品标志：
  C
• 安全说明：
  S26,S36/37/39,S45
• 危险类别码：
  R34
• WGK Germany：
  3
• 海关编码：
  29159080
• 包装等级：
  II
• 危险类别：
  8
• 危险标志：
  GHS05
• 危险品运输编号：
  UN 3265 8/PG 2
• 危险性描述：
  H314
• 危险性防范说明：
  P280,P305 + P351 + P338,P310
• 储存条件：
  室温

SDS

---

Section 1. IDENTIFICATION OF THE SUBSTANCE/MIXTURE
Product identifiers
Product name : Pentadecafluorooctanoyl chloride
CAS-No. : 335-64-8
Relevant identified uses of the substance or mixture and uses advised against
Identified uses : Laboratory chemicals, Manufacture of substances

---

Section 2. HAZARDS IDENTIFICATION
Classification of the substance or mixture
Classification according to Regulation (EC) No 1272/2008 [EU-GHS/CLP]
Skin corrosion (Category 1B)
Classification according to EU Directives 67/548/EEC or 1999/45/EC
Causes burns.
Label elements
Labelling according Regulation (EC) No 1272/2008 [CLP]
Pictogram
Signal word Danger
Hazard statement(s)
H314 Causes severe skin burns and eye damage.
Precautionary statement(s)
P280 Wear protective gloves/ protective clothing/ eye protection/ face
protection.
P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove
contact lenses, if present and easy to do. Continue rinsing.
P310 Immediately call a POISON CENTER or doctor/ physician.
Supplemental Hazard none
Statements
According to European Directive 67/548/EEC as amended.
Hazard symbol(s)
R-phrase(s)
R34 Causes burns.
S-phrase(s)
S26 In case of contact with eyes, rinse immediately with plenty of water and
seek medical advice.
S36/37/39 Wear suitable protective clothing, gloves and eye/face protection.
S45 In case of accident or if you feel unwell, seek medical advice immediately
(show the label where possible).
Other hazards
Lachrymator.

---

Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Substances
Formula : C8ClF15O
Molecular Weight : 432,51 g/mol
Component Concentration
Pentadecafluorooctyl chloride
CAS-No. 335-64-8 -
EC-No. 206-394-2

---

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
Take off contaminated clothing and shoes immediately. Wash off with soap and plenty of water. Consult a
physician.
In case of eye contact
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
If swallowed
Do NOT induce vomiting. 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
Material is extremely destructive to tissue of the mucous membranes and upper respiratory tract, eyes, and
skin., spasm, inflammation and edema of the larynx, spasm, inflammation and edema of the bronchi,
pneumonitis, pulmonary edema, burning sensation, Cough, wheezing, laryngitis, Shortness of breath,
Headache, Nausea
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
Carbon oxides, Hydrogen chloride gas, Hydrogen fluoride
Advice for firefighters
Wear self contained breathing apparatus for fire fighting if necessary.
Further information
no data available

---

Section 6. ACCIDENTAL RELEASE MEASURES
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment. Avoid breathing vapors, mist or gas. Ensure adequate ventilation.
Evacuate personnel to safe areas.
Environmental precautions
Do not let product enter drains.
Methods and materials for containment and cleaning up
Soak up with inert absorbent material and dispose of as hazardous waste. 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 inhalation of vapour or mist.
Normal measures for preventive fire protection.
Conditions for safe storage, including any incompatibilities
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Containers which are
opened must be carefully resealed and kept upright to prevent leakage.
Moisture sensitive.
Specific end use(s)
no data available

---

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
Tightly fitting safety goggles. Faceshield (8-inch minimum). 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
Where risk assessment shows air-purifying respirators are appropriate use a full-face respirator
with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup
to engineering controls. If the respirator is the sole means of protection, use a full-face supplied air
respirator. Use respirators and components tested and approved under appropriate government
standards such as NIOSH (US) or CEN (EU).

---

Section 9. PHYSICAL AND CHEMICAL PROPERTIES
Information on basic physical and chemical properties
a) Appearance Form: liquid
Colour: colourless
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 129 - 130 °C at 992 hPa - lit.
boiling range
g) Flash point 113 °C - closed cup
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 1,744 g/cm3 at 25 °C
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
no data available
Possibility of hazardous reactions
no data available
Conditions to avoid
no data available
Incompatible materials
Strong oxidizing agentsStrong oxidizing agents, Strong bases
Hazardous decomposition products
Other decomposition products - no data available

---

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 sensitization
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
Potential health effects
Inhalation May be harmful if inhaled. Material is extremely destructive to the tissue of
the mucous membranes and upper respiratory tract.
Ingestion May be harmful if swallowed. Causes burns.
Skin May be harmful if absorbed through skin. Causes skin burns.
Eyes Causes eye burns.
Signs and Symptoms of Exposure
Material is extremely destructive to tissue of the mucous membranes and upper respiratory tract, eyes, and
skin., spasm, inflammation and edema of the larynx, spasm, inflammation and edema of the bronchi,
pneumonitis, pulmonary edema, burning sensation, Cough, wheezing, laryngitis, Shortness of breath,
Headache, Nausea
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
no data available
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. Contact a licensed
professional waste disposal service to dispose of this material.
Contaminated packaging
Dispose of as unused product.

---

Section 14. TRANSPORT INFORMATION
UN number
ADR/RID: 3265 IMDG: 3265 IATA: 3265
UN proper shipping name
ADR/RID: CORROSIVE LIQUID, ACIDIC, ORGANIC, N.O.S. (Pentadecafluorooctyl chloride)
IMDG: CORROSIVE LIQUID, ACIDIC, ORGANIC, N.O.S. (Pentadecafluorooctyl chloride)
IATA: Corrosive liquid, acidic, organic, n.o.s. (Pentadecafluorooctyl chloride)
Transport hazard class(es)
ADR/RID: 8 IMDG: 8 IATA: 8
Packaging group
ADR/RID: II IMDG: II IATA: II
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
no data available

---

Section 16. OTHER INFORMATION
Further information
Copyright 2012 Co. LLC. License granted to make unlimited paper copies for internal use
only.
The above information is believed to be correct but does not purport to be all inclusive and shall be
used only as a guide. The information in this document is based on the present state of our knowledge
and is applicable to the product with regard to appropriate safety precautions. It does not represent any
guarantee of the properties of the product. Corporation and its Affiliates shall not be held
liable for any damage resulting from handling or from contact with the above product. See
and/or the reverse side of invoice or packing slip for additional terms and conditions of sale.

反应信息

• 作为反应物：
  描述：

  全氟辛酰氯 在 sodium hydroxide 、 双氧水 作用下， 以 1,1,2-三氯三氟乙烷（CFC-113） 为溶剂， 以70%的产率得到bis(pentadecafluoro-octanoyl) peroxide
  参考文献：
  名称：

  Thermal decomposition of some perfluoro- and polyfluorodiacyl peroxides

  摘要：

  DOI：

  10.1021/jo00132a007
• 作为产物：
  描述：

  全氟辛酸 在 苯甲酰氯 作用下， 以77%的产率得到全氟辛酰氯
  参考文献：
  名称：

  α，α-二卤代氟甲基全氟烷基酮的区域特异性制备

  摘要：

  -磷鎓盐与-酰氯的酰化以高收率得到相应的-全氟甜菜碱。随后的氯化或溴化区域特异性地产生α，α-二卤代氟甲基全氟烷基酮。

  DOI：

  10.1016/s0040-4039(00)83859-9

文献信息

• Synthesis and antimalarial activity of new 4-amino-7-chloroquinolyl amides, sulfonamides, ureas and thioureas
  作者：Kekeli Ekoue-Kovi、Kimberly Yearick、Daniel P. Iwaniuk、Jayakumar K. Natarajan、John Alumasa、Angel C. de Dios、Paul D. Roepe、Christian Wolf

  DOI：10.1016/j.bmc.2008.11.009

  日期：2009.1

  We report the synthesis and in vitro antimalarial activities of more than 50 7-chloro-4-aminoquinolyl-derived sulfonamides 3–8 and 11–26, ureas 19–22, thioureas 23–26, and amides 27–54. Many of the CQ analogues prepared for this study showed submicromolar antimalarial activity versus HB3 (chloroquine sensitive) and Dd2 (chloroquine resistant strains of Plasmodium falciparum) and low resistance indices

  我们报告了 50 多种 7-氯-4-氨基喹啉衍生的磺酰胺3 – 8和11 – 26、尿素19 – 22、硫脲23 – 26和酰胺27 – 54的合成和体外抗疟活性。许多为本研究制备的 CQ 类似物显示出亚微摩尔级抗疟活性，而 HB3（对氯喹敏感）和 Dd2（恶性疟原虫的氯喹抗性菌株）) 和低电阻指数在大多数情况下获得。侧链长度的系统变化和氟化脂肪族和芳香族末端的引入揭示了克服 CQ 抗性的有希望的线索。特别是，磺酰胺3具有短侧链和末端丹磺酰部分，结合了高抗疟原虫效力和低抗性指数，对 HB3 和 Dd2 寄生虫的IC 50 s 分别为 17.5 和 22.7 nM。
• An Efficient, Overall [4+1] Cycloadditon of 1,3-Dienes and Nitrene Precursors
  作者：Qiong Wu、Jian Hu、Xinfeng Ren、Jianrong Steve Zhou

  DOI：10.1002/chem.201101630

  日期：2011.10.4

  Intermolecular cycloadditions of conjugated dienes and nitrene precursors usually produce aziridines. A generally useful method was lacking to directly provide the [4+1] cycloadducts, 3‐pyrrolines. We have realized this transformation by using an uniquely active catalyst, copper(II) 1,1,1,5,5,5‐hexafluoroacetylacetonate ([Cu(hfacac)2]). The method is applicable to a wide array of dienes with good yields

  共轭二烯和腈前体的分子间环加成通常产生氮丙啶。缺少直接提供[4 + 1]环加合物，3-吡咯啉的通用方法。我们已经通过使用独特的活性催化剂1，（1,2,1,1,1,5,5,5,5-六氟乙酰丙酮铜（[Cu（hfacac）2 ]））实现了这种转变。该方法适用于多种具有良好产率的二烯。当使用1,4-二取代的二烯作为底物时，可以获得很好的顺式或反式选择性。有趣的是，顺式或反式优选取决于取代基的性质，而不是二烯的几何形状。机理研究表明，[4 + 1]环加成反应是通过二烯叠氮化和随后的环扩展进行的。在普通的铜催化剂中，只有[Cu（hfacac）2 ]可以有效地催化两个步骤，这说明了该催化剂的独特效率。
• Hydrophobic effects on photochemical and photophysical processes: evidence for aggregation of perfluorocarbon in aqueous–organic solvents
  作者：Chen-Ho Tung、Hai-Feng Ji

  DOI：10.1039/ft9959102761

  日期：——

  spectra and photodimerization of fluorinated alkyl 2-naphthoates (NpFCn) and 9-anthrylmethyl perfluoroalkanoates (AnFCn) in aqueous–organic binary solvents have been investigated. The fluorescence spectra of NpFCn in dimethyl sulfoxide–water mixture (DMSO–H2O) are dominated by excimer emission. Addition of long chain fluorocarbon compounds to the solution results in a reduction in the excimer emission

  氟化烷基-2-萘（NPFC的发射光谱和光二Ñ）和9-蒽甲基perfluoroalkanoates（AnFC Ñ在水-有机溶剂的二进制）进行了研究。NpFC n在二甲亚砜-水混合物（DMSO-H 2 O）中的荧光光谱受准分子发射支配。向溶液中加入长链碳氟化合物可减少受激准分子的发射并增加单体的发射。在NPFC的混合物溶液中的萘部分的有选择性的激励Ñ和AnFC Ñ从AnFC导致强发射Ñ。NpFC n的光辐照产生具有相对高量子产率的“类古巴”光电二聚体。所有这些观察结果表明，疏水相互作用迫使带有长碳氟化合物链的分子在水性有机二元溶剂中形成聚集体。
• Fluorous-tag assisted synthesis of bile acid–bisphosphonate conjugates via orthogonal click reactions: an access to potential anti-resorption bone drugs
  作者：Chiara Massarenti、Olga Bortolini、Giancarlo Fantin、Dario Cristofaro、Daniele Ragno、Daniela Perrone、Elena Marchesi、Gianluca Toniolo、Alessandro Massi

  DOI：10.1039/c7ob00774d

  日期：——

  candidates is reported. The disclosed methodology relied on the installation of azide and thiol functionalities at the head and tail positions, respectively, of the BA scaffold and its subsequent decoration by orthogonal click reactions (copper-catalyzed azide–alkyne cycloaddition, thiol–ene or thiol–yne coupling) to introduce BP units and a fluorophore. Because of the troublesome isolation of the target

  据报道，合成了少量新的胆汁酸-双膦酸盐（BA-BP）偶联物作为潜在的候选药物。所披露的方法分别依赖于BA支架的头尾位置上的叠氮化物和硫醇官能团的安装以及随后通过正交点击反应（铜催化的叠氮化物-炔环加成，硫醇-烯或硫醇-炔偶联）的修饰）引入BP单元和荧光团。由于通过标准程序难以分离靶标结合物，因此该方法最终以具有轻质荧光标签的BA支架功能化，从而通过荧光固相萃取快速有效地纯化中间体和最终产物。
• Potential antiatherosclerotic agents. 4. [(Functionalized-alkyl)amino]benzoic acid analogs of cetaben
  作者：Vern G. DeVries、Elwood E. Largis、Thomas G. Miner、Robert G. Shepherd、Janis Upeslacis

  DOI：10.1021/jm00364a011

  日期：1983.10

  the alkyl group of cetaben is substituted with various functional groups or replaced entirely by a functionalized alkanoyl moiety is described. Also reported are the syntheses of branched-chain (alkylamino)benzoic acids in which branching is specifically localized at the terminus of the alkyl chain. Structure-activity relationships of these compounds, both as hypolipidemic agents and as inhibitors of

  描述了一系列类似物的合成，其中cetaben的烷基被各种官能团取代或完全被官能化的烷酰基部分取代。还报道了支链（烷基氨基）苯甲酸的合成，其中支化特别地位于烷基链的末端。讨论了这些化合物的结构活性关系，这些化合物既作为降血脂药，又作为脂肪酰基辅酶A：胆固醇酰基转移酶（ACAT）的抑制剂。专门合成了某些化合物以检验以下假设：位于Cetaben烷基链末端附近的基团可能会延迟分子的代谢降解，从而增强生物活性。发现其中一些（48-50）是合成的最活跃的类似物。

表征谱图