Methyl 2-Cyanoacrylate Hazard Summary

Total Page:16

File Type:pdf, Size:1020Kb

Methyl 2-Cyanoacrylate Hazard Summary Common Name: METHYL 2-CYANOACRYLATE CAS Number: 137-05-3 RTK Substance number: 1241 DOT Number: None Date: April 1986 Revision: February 2000 ----------------------------------------------------------------------- ----------------------------------------------------------------------- HAZARD SUMMARY * Methyl 2-Cyanoacrylate can affect you when breathed in * ODOR THRESHOLD = 2.2 ppm. and may be absorbed through the skin. * The range of accepted odor threshold values is quite * Contact can irritate and burn the skin and eyes. broad. Caution should be used in relying on odor alone as * Breathing Methyl 2-Cyanoacrylate can irritate the nose a warning of potentially hazardous exposures. and throat causing coughing and wheezing. * Methyl 2-Cyanoacrylate may cause a skin allergy. If WORKPLACE EXPOSURE LIMITS allergy develops, very low future exposure can cause NIOSH: The recommended airborne exposure limit is itching and a skin rash. 2 ppm averaged over a 10-hour workshift and * Methyl 2-Cyanoacrylate may cause an asthma-like 4 ppm not to be exceeded during any 15 minute allergy. Future exposure can cause asthma attacks with work period. shortness of breath, wheezing, cough, and/or chest tightness. ACGIH: The recommended airborne exposure limit is 0.2 ppm averaged over an 8-hour workshift. IDENTIFICATION Methyl 2-Cyanoacrylate, also called “Super Glue,” is a thick * The above exposure limits are for air levels only. When clear liquid with an irritating odor. It is used in adhesives and skin contact also occurs, you may be overexposed, even in dentistry. though air levels are less than the limits listed above. REASON FOR CITATION WAYS OF REDUCING EXPOSURE * Methyl 2-Cyanoacrylate is on the Hazardous Substance * Where possible, enclose operations and use local exhaust List because it is cited by ACGIH and NIOSH. ventilation at the site of chemical release. If local exhaust * Definitions are provided on page 5. ventilation or enclosure is not used, respirators should be worn. HOW TO DETERMINE IF YOU ARE BEING * Wear protective work clothing. EXPOSED * Wash thoroughly immediately after exposure to Methyl 2- The New Jersey Right to Know Act requires most employers Cyanoacrylate and at the end of the workshift. to label chemicals in the workplace and requires public * Post hazard and warning information in the work area. In employers to provide their employees with information and addition, as part of an ongoing education and training training concerning chemical hazards and controls. The effort, communicate all information on the health and federal OSHA Hazard Communication Standard, 1910.1200, safety hazards of Methyl 2-Cyanoacrylate to potentially requires private employers to provide similar training and exposed workers. information to their employees. * Exposure to hazardous substances should be routinely evaluated. This may include collecting personal and area air samples. You can obtain copies of sampling results from your employer. You have a legal right to this information under OSHA 1910.1020. * If you think you are experiencing any work-related health problems, see a doctor trained to recognize occupational diseases. Take this Fact Sheet with you. METHYL 2-CYANOACRYLATE page 2 of 6 This Fact Sheet is a summary source of information of all Any evaluation should include a careful history of past and potential and most severe health hazards that may result from present symptoms with an exam. Medical tests that look for exposure. Duration of exposure, concentration of the damage already done are not a substitute for controlling substance and other factors will affect your susceptibility to exposure. any of the potential effects described below. --------------------------------------------------------------------------- Request copies of your medical testing. You have a legal right to this information under OSHA 1910.1020. HEALTH HAZARD INFORMATION Mixed Exposures Acute Health Effects * Because smoking can cause heart disease, as well as lung The following acute (short-term) health effects may occur cancer, emphysema, and other respiratory problems, it may immediately or shortly after exposure to Methyl 2- worsen respiratory conditions caused by chemical Cyanoacrylate: exposure. Even if you have smoked for a long time, stopping now will reduce your risk of developing health * Contact can irritate and burn the skin and eyes. problems. * Breathing Methyl 2-Cyanoacrylate can irritate the nose and throat causing coughing and wheezing. WORKPLACE CONTROLS AND PRACTICES Chronic Health Effects Unless a less toxic chemical can be substituted for a hazardous The following chronic (long-term) health effects can occur at substance, ENGINEERING CONTROLS are the most some time after exposure to Methyl 2-Cyanoacrylate and can effective way of reducing exposure. The best protection is to last for months or years: enclose operations and/or provide local exhaust ventilation at the site of chemical release. Isolating operations can also Cancer Hazard reduce exposure. Using respirators or protective equipment is * According to the information presently available to the less effective than the controls mentioned above, but is New Jersey Department of Health and Senior Services, sometimes necessary. Methyl 2-Cyanoacrylate has not been tested for its ability to cause cancer in animals. In evaluating the controls present in your workplace, consider: (1) how hazardous the substance is, (2) how much of the Reproductive Hazard substance is released into the workplace and (3) whether * According to the information presently available to the harmful skin or eye contact could occur. Special controls New Jersey Department of Health and Senior Services, should be in place for highly toxic chemicals or when Methyl 2-Cyanoacrylate has not been tested for its ability significant skin, eye, or breathing exposures are possible. to affect reproduction. In addition, the following control is recommended: Other Long-Term Effects * Methyl 2-Cyanoacrylate may cause a skin allergy. If * Where possible, automatically pump liquid Methyl 2- allergy develops, very low future exposure can cause Cyanoacrylate from drums or other storage containers to itching and a skin rash. process containers. * Methyl 2-Cyanoacrylate may cause an asthma-like allergy. Future exposure can cause asthma attacks with Good WORK PRACTICES can help to reduce hazardous shortness of breath, wheezing, cough, and/or chest exposures. The following work practices are recommended: tightness. * Workers whose clothing has been contaminated by MEDICAL Methyl 2-Cyanoacrylate should change into clean clothing promptly. Medical Testing * Contaminated work clothes should be laundered by individuals who have been informed of the hazards of If symptoms develop or overexposure is suspected, the exposure to Methyl 2-Cyanoacrylate. following are recommended: * Eye wash fountains should be provided in the immediate work area for emergency use. * Evaluation by a qualified allergist, including careful * If there is the possibility of skin exposure, emergency exposure history and special testing, may help diagnose shower facilities should be provided. skin allergy. * On skin contact with Methyl 2-Cyanoacrylate, * Lung function tests. These may be normal if the person is immediately wash or shower to remove the chemical. At not having an attack at the time of the test. the end of the workshift, wash any areas of the body that may have contacted Methyl 2-Cyanoacrylate, whether or not known skin contact has occurred. METHYL 2-CYANOACRYLATE page 3 of 6 * Do not eat, smoke, or drink where Methyl 2- QUESTIONS AND ANSWERS Cyanoacrylate is handled, processed, or stored, since the chemical can be swallowed. Wash hands carefully before Q: If I have acute health effects, will I later get chronic eating, drinking, smoking, or using the toilet. health effects? A: Not always. Most chronic (long-term) effects result PERSONAL PROTECTIVE EQUIPMENT from repeated exposures to a chemical. WORKPLACE CONTROLS ARE BETTER THAN Q: Can I get long-term effects without ever having short- PERSONAL PROTECTIVE EQUIPMENT. However, for term effects? some jobs (such as outside work, confined space entry, jobs A: Yes, because long-term effects can occur from repeated done only once in a while, or jobs done while workplace exposures to a chemical at levels not high enough to controls are being installed), personal protective equipment make you immediately sick. may be appropriate. Q: What are my chances of getting sick when I have been OSHA 1910.132 requires employers to determine the exposed to chemicals? appropriate personal protective equipment for each hazard and A: The likelihood of becoming sick from chemicals is to train employees on how and when to use protective increased as the amount of exposure increases. This is equipment. determined by the length of time and the amount of material to which someone is exposed. The following recommendations are only guidelines and may not apply to every situation. Q: When are higher exposures more likely? A: Conditions which increase risk of exposure include Clothing physical and mechanical processes (heating, pouring, * Avoid skin contact with Methyl 2-Cyanoacrylate. Wear spraying, spills and evaporation from large surface areas protective gloves and clothing. Safety equipment such as open containers), and "confined space" suppliers/ manufacturers can provide recommendations on exposures (working inside vats, reactors, boilers, small the most protective glove/clothing material for your rooms, etc.). operation.
Recommended publications
  • (12) United States Patent (10) Patent No.: US 6,699,940 B2 Shalaby (45) Date of Patent: Mar
    USOO66.9994OB2 (12) United States Patent (10) Patent No.: US 6,699,940 B2 Shalaby (45) Date of Patent: Mar. 2, 2004 (54) CYANOACRYLATE-CAPPED (56) References Cited HETEROCHAIN POLYMERS AND TISSUE ADHESIVES AND SEALANTS THEREFROM U.S. PATENT DOCUMENTS 4,260,719 A * 4/1981 Ching ........................ 528/196 (75) Inventor: Shalaby W. Shalaby, Anderson, SC 4,377,490 A * 3/1983 Shiraishi et al. ...... 252/188.3 R (US) 5,340,873 A * 8/1994 Mitry .......................... 525/10 5,350,798 A 9/1994 Linden et al. ................ 525/41 (73) Assignee: Poly Med, Inc., Anderson, SC (US) 5,373,035 A * 12/1994 Uemura et al. ............. 523/212 5,422,068 A 6/1995 Shalaby et al. ............... 422/22 (*) Notice: Subject to any disclaimer, the term of this 5,653,992 A 8/1997 Bezwada et al. ............ 264/4.3 5,714,159 A 2/1998 Shalaby ...................... 424/426 patent is extended or adjusted under 35 U.S.C. 154(b) by 0 days. 6,299,631 B1 10/2001 Shalaby ...................... 606/214 6,462,169 B1 10/2002 Shalaby ...................... 528/354 (21) Appl. No.: 10/300,079 6,467,169 B1 10/2002 Wieres ........................ 29/890 (22) Filed: Nov. 20, 2002 * cited by examiner (65) Prior Publication Data Primary Examiner Helen L. Pezzuto US 2003/0105256 A1 Jun. 5, 2003 (74) Attorney, Agent, or Firm-Leigh P. Gregory Related U.S. Application Data (57) ABSTRACT (60) Provisional application No. 60/335,439, filed on Dec. 4, The present invention is directed toward cyanoacrylate 2001. based tissue adhesive or Sealant compositions comprising (51) Int.
    [Show full text]
  • Born2bond Structural Cyanoacrylate Adhesive
    Born2Bond Structural Cyanoacrylate Adhesive Description Born2Bond™ Structural Cyanoacrylate Adhesive is a high-strength, high-temperature (120°C) hybrid cyanoacrylate adhesive that provides a fast fixture time at room temperature while maintaining good processability and the capability to bond gaps up to 5mm. This product offers excellent bonding characteristics to a large variety of substrates, including aluminium, plastics and elastomers, but also porous substrates, such as woods, chipboard and leather. Born2Bond Structural is the toughest structural, fast cure two part (2K) cyanoacrylate adhesive on the market, with the longest open time. Born2Bond Structural offers “on demand” structural bonding. Once mixed and applied, the exposed dot or bead has an open time of up to 30 minutes – but a fixture time of only seconds once the parts are assembled. This fixture and ultimate cure time compares favourably with other structural adhesive chemistries. Formulated using MECA (methoxyethyl cyanoacrylate) chemistry, Born2Bond Structural is able to withstand temperatures up to 120°C, far exceeding the capabilities of standard cyanoacrylate adhesives. It offers a balance between bonding speed, long open time, bond strength (>6 MPa), and impact and environmental resistance. Born2Bond Structural is supplied in a syringe cartridge, available in 10g and 50g sizes. Both cartridges come with static mixing nozzles. The 10g size is suitable for manual application and comes with a plunger. The 50g size is used with a dispensing gun for manual application,
    [Show full text]
  • Dispensing Solutions for Cyanoacrylate Adhesives White
    Dispensing Solutions for Cyanoacrylate Adhesives Contents How Cyanoacrylates Work .......................................................................3 Advantages of CAs ...................................................................................4 CA Dispensing Challenges .......................................................................4 Best Practices for Dispensing CAs .....................................................5-12 Best Systems for Dispensing CAs ....................................................13-14 Useful Resources ...................................................................................15 Introduction Cyanoacrylate adhesives, also known as CAs or cyanos, are highly effective at bonding many types of materials together in assembly processes. Often referred to as super glues, they exhibit high bond strength and fast cure times that help manufacturers speed production processes for higher throughput yields. This makes them an ideal choice for assembling products in a variety of industries, including automotive, electronics, life sciences, defense, and consumer goods. Though beneficial, these moisture-cure adhesives can be a challenge, especially when your assembly process requires precise, repeatable dispensing. This paper outlines proper handling methods and dispensing solutions for successful CA dispensing. Find out how to minimize material waste by more than 60% while also minimizing operator exposure to the adhesive. Speed your production processes while producing higher quality parts with
    [Show full text]
  • Technical Procedure for Cyanoacrylate Ester Fingerprint
    Technical Procedure for Cyanoacrylate Ester Fingerprint Development Kits Version 5 Latent Evidence Section Effective Date: 02/01/2019 Issued by Latent Technical Leader Technical Procedure for Cyanoacrylate Ester Fingerprint Development Kits 1.0 Purpose – This procedure is a non-porous development procedure. 2.0 Scope – This procedure is a step in the processing of non-porous evidence that may contain impressions that require developing/enhancing. 2.1 The Cyanoacrylate Ester Fingerprint Development Kit is a commercially prepared product that polymerizes the latent impression using cyanoacrylate. Numerous materials, including plastic bags, weapons, metals, and various other substrates, may be processed using the Cyanoacrylate Ester Fingerprint Development Kit. Cyanoacrylate shall be used as a preliminary process for subsequent processing techniques. Fluorescent dye staining, in conjunction with laser examinations, is dependent on the proper use of cyanoacrylate fuming techniques. 3.0 Definitions Alternate light source: Any of the multiple forensic light sources readily available in the Latent Evidence Section including, but not limited to, the CrimeScope (CS), Mini-CrimeScope (MCS), and TracER Laser. Ambient light: Light that is readily available in the office environment (i.e., natural light or light that emanates from an office lighting source). CE: Cyanoacrylate ester, also known as super glue. Cyanoacrylate Ester Fingerprint Development Kit: A commercially prepared cyanoacrylate ester fuming kit that assists in the processing of non-porous items of evidence with the assistance of cyanoacrylate ester. Commercial products currently used include Hot-Shot by Lynn Peavey and Cyano- Shot by Sirchie. 4.0 Equipment, Materials and Reagents 4.1 Equipment and Materials Cyanoacrylate Ester Fingerprint Development Kit 4.2 Reagents – N/A 5.0 Procedure 5.1 Hot-Shot (Lynn Peavey Product): 5.1.1 Items to be processed with the Hot-Shot shall first be examined visually in ambient lighting conditions and then with the use of an alternate light source (CS, MCS).
    [Show full text]
  • Technical Data Sheet Permatex® Plastic & Rubber Cyanoacrylate
    Unit 3 Shipton Way Technical Data Sheet Express Business Park Permatex® Plastic & Rubber Northampton Road Rushden, NN10 6GL Cyanoacrylate Adhesive. Tel: 0870 458 9686 PRODUCT DESCRIPTION PROPERTIES OF UNCURED MATERIAL Permatex Plastic & Rubber Cyanoacrylate Adhesive is a Typical Value low viscosity Ethyl Cyanoacrylate adhesive. Permatex Chemical Type Ethyl Plastic & Rubber Cyanoacrylate Adhesive is formulated for Appearance Clear high strength, high speed bonding of plastics and rubbers. Specific Gravity 1.06 Viscosity cPs¹ PRODUCT BENEFITS - range 17-22 • Fast cure speed - typical value 20 • Bonds most plastic and rubbers Tensile Strength², typical (N/mm²) 20 • Can be post applied to pre assembled parts Fixture Time (seconds) 2-20 Full Cure (hours) 24 DIRECTIONS FOR USE Flash point (ºC) >85 1. Both surfaces must be smooth, clean, dry and free of Shelf Life @ 5 ºC (months) 12 oil, grease, etc. Max Gap Fill (mm) 0.10 2. USE EXTREME CARE WHEN OPENING. Hold bottle Operating Temperature Range (ºC) -50 to +80 upright, pointing away from face. Remove nozzle. 3. Apply adhesive to one surface, about one drop per ¹ISO 3104/3105 square inch. Spread evenly. ²ISO 6922 4. Immediately place the second surface in contact with the first surface and press together. TYPICAL CURING PERFORMANCE 5. Keep light pressure on surfaces for 15 seconds or until Substrate Cure time, seconds. bond sets. DO NOT REPOSITION THE PARTS. Steel/Steel <20 6. Allow to completely harden, for best results, overnight. ABS/ABS <10 NOTE: Not suitable for untreated polyethylene or Rubber/Rubber <5 polypropylene products. Cure speed vs. substrate FOR CLEANUP The cure speed of cyanoacrylates vary according to the 1.
    [Show full text]
  • PERMABOND® 260 Cyanoacrylate Ref
    PERMABOND ® 260 Cyanoacrylate Ref. #: 041509PB260 FEATURES & BENEFITS TYPICAL APPLICATION ¨ Instant Setting Rubber bonding ¨ Improved Gap Filling Bonding of passivated metals ¨ Faster Strength Development ¨ Improved Bonding to Difficult Surfaces ¨ High Shear Strength ¨ Easy to Apply ¨ One Part System GENERAL DESCRIPTION PERMABOND 260 is a low viscosity cyanoacrylate ideal fro wicking type application. PERMABOND 260 provides faster set times and improved gap­filling capability compared to conventional cyanoacrylates. The adhesive bonds to a wide range of substrates including metals, ceramics, plastics and elastomers. It is excellent for bonding difficult­to­bond plastics such as polyacetals. PHYSICAL PROPERTIES OF THE UNCURED ADHESIVE Chemical Type Ethyl Color Colorless Viscosity, cP @ 25°C 2 Specific Gravity 1.05 Flash point, °C (°F) 83 (181) Shelf Life stored at 2°C – 7°C (35°F – 45°F), months 12 Maximum gap fill; in (mm) .002 (0.05) Non­Warranty: The information given and the recommendations made herein are based on our research and are believed to be accurate but no guarantee of their accuracy is made. In every case we urge and recommend that purchasers before using any product in full­scale production make their own tests to determine to their own satisfaction whether the product is of acceptable quality and is suitable for their particular purpose under their own operating conditions. THE PRODUCTS DISCLOSED HEREIN ARE SOLD WITHOUT ANY WARRANTY AS TO MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE OR ANY OTHER WARRANTY, EXPRESS OR IMPLIED. No representative of ours has any authority to waive or change the foregoing provisions but, subject to such provisions, our engineers are available to assist purchasers in adapting our products to their needs and to the circumstances prevailing in their business.
    [Show full text]
  • Nomination Background: Ethyl Cyanoacrylate (CASRN: 7085-85-0)
    i' ETHYL CYANOACRYLATE CAS Number: 7085-85-0 NTP Nomination History and Review NCI summary of·oata for Chemical Selection Ethyl cyanoacrylate 7085-85-0 NTP NOMINATION HISTORY AND REVIEW A. Nomination History 1. Source: National Cancer Institute 2. Reco~endation: -Carcinogenicity (Inhalation) -Neurotoxicity -Reproductive and developmental effects 3. Rationale/Remarks: -Widespread use as a consumer instant adhesive -Lack of toxicity data -Potential biological activity 4. Priority: High 5. Date of Nomination: 5/91 B. Chemical Evaluation Committee Review 1. Date of Review: 2. Recommendations: 3. Priority: 4. NTP Chemical Selection Principles: 5. Rationale/Remarks: c. Board of Scientific Counselors Review 1. Date of Review: 2. Recommendations: 3. Priority: 4. Rationale/Remarks: D. Executive Committee Review 1. Date of Review: 2. Decision: . \ ,. 7085-85-0 Ethyl cyanoacrylate SUMMARY OF DATA FOR CHEMICAL SELECTION CHEMICAL IDENTIFICATION CAS Registry Number: 7085-85-0 Chern. Abstr. Name: 2-Cyano-2-propenoic acid, ethyl ester Synonyms & Trade Names: 910EM; ACE-EE; ACE-E SO; acrylic acid, 2-cyano-, ethyl ester; adhesive 502; Aron Alpha D; Black Max; CA 3; CA 3 (adhesive); CA 8-3A; CN 2; CN 4; Cemedine 3000RP; Cemedine 3000RP Type-II; Cemedine 3000RS; Cemedine 3000RS Type-11; Cyanobond W 100; Cyanobond W 300; Cyanolite 20 1; Cyan on 5MSP; DA 737S; ethyl Q-cyanoacrylate; ethyl 2-cyanoacrylate; Krazy Glue; N 135; Permabond 105; Permabond 200; Permabond 268; Pro Grip 4000; PTR-E 3; PTR-E 40; Super 3-1000; Superbonder 420; Super Glue; TK. 200; TK 201 Structure. Molecular Formula and Molecular Weight Mol. wt.: 125.13 Chemical and Physical Properties [From Coover eta/.
    [Show full text]
  • Determination of the Kinetics of Curing of Cyanoacrylate-Based Adhesives with Fourier Transform Infrared Spectroscopy
    CPGAN #001 Kinetics of Curing of Adhesives ©Cambridge Polymer Group, Inc.(2004). All rights reserved. Determination of the Kinetics of Curing of Cyanoacrylate-based Adhesives with Fourier Transform Infrared Spectroscopy Background Cyanoacrylate-based adhesives are low-viscosity, rapid curing adhesives that are commonly used for quick fix applications. They cure within a few minutes, and provide a brittle, non-space filling bond between two subtrates. The adhesives rely on moisture to initiate the curing reaction. Chemistry Cyanoacrylate cements contain a monomer group possessing an unsaturated carbon-carbon bond. The monomer is stabilized with a weak acid to prevent curing in the container. To initiate the reaction, the acid stabilizer must be neutralized with a weak base. Airborne or surface adsorbed water is usually sufficient to neutralize the weak base, although an alkaline surface will also suffice. The amino acid content in skin, in addition to the water content, initiates the polymerization reaction very well. Once the stabilizer is neutralized by the water, the monomer polymerizes via an anionic reaction. Only a small amount of water is necessary to catalyze the initiation reaction. As the monomer polymerizes, the carbon-carbon double bond is consumed, as shown in Figure 1. Figure 1: Initiation and propagation reactions for cyanoacrylate-based adhesives when exposed to a weak base. Reaction Kinetics In order to monitor the polymerization kinetics of cyanoacrylate adhesives, we often employ Fourier Transform Infrared Spectroscopy (FTIR). FTIR is used to identify and quantify chemical groups, such as C-H bonds or C=C bonds, which absorb infrared light at specific wavelengths. By identifying a specific chemical group that is consumed in a chemical reaction, FTIR can be used to monitor the kinetics and extent of reaction.
    [Show full text]
  • Reactive Polymers Fundamentals and Applications
    Propery of Reed Elsevier 13 Cyanoacrylates Cyanoacrylates were commercially introduced in for polymerization. Instead of aqueous formaldehyde, 1950 by Tennesee Eastman Company. Cyanoacrylate paraformaldehyde was used with an organic solvent to adhesives are monomeric adhesives. They are gener- remove the water by azeotropic distillation. The sta- ally quick-setting materials which cure to clear, hard bility of the monomer can be enhanced by the redistil- glassy resins, useful as sealants, coatings, and par- lation of the crude monomer in the presence of small ticularly adhesives for bonding together a variety of quantities of acidic stabilizers, e.g., sulfur dioxide. substrates [1]. Polymers of alkyl 2-cyanoacrylates are Several other methods for cyanoacrylate monomer also known as superglues. production have been described, including the pyro- In addition to their use as adhesives, cyanoacrylates lysis of 3-alkoxy-2-cyanopropionates [8], transester- have been reported to have highly herbicidal prop- ification of ethyl cyanoacrylate [9], and displacement erties, as they disrupt photosynthetic electron trans- of cyanoacrylate monomer from its anthracene Diels- portation [2–4]. Alder adduct by treatment with maleic anhydride. This last method is used for the synthesis of monomers 13.1 Monomers that are not accessible or may be difficult to prepare by the retropolymerization route, for example difunc- 13.1.1 Synthesis tional cyanoacrylates [10], thiocyanoacrylates [11], and perfluorinated monomers. In 1895 von Auwers and Thorpe [5] attempted to synthesize diethyl-2,2-dicyanoglutarate (Figure 13.1) by base-catalyzed condensation of aqueous formalde- 13.1.2 Crosslinkers hyde and ethyl cyanoacetate. They isolated a mixture To improve the cohesive strength, difunctional mono- of oily oligomers and an amorphous polymer of higher meric crosslinking agents may be added to the mono- molecular weight.
    [Show full text]
  • M-Bond 200 Adhesive August 30, 2004
    MATERIAL SAFETY DATA SHEET SECTION 1: CHEMICAL PRODUCT AND COMPANY IDENTIFICATION PRODUCT: M-Bond 200 Adhesive August 30, 2004 Vishay Micro-Measurements MSDS # MGM007P Post Office Box 27777 Raleigh, NC 27611 919-365-3800 CHEMTREC 1-800-424-9300 (U.S.) 703-527-3887 (Outside U.S.) NOTE: CHEMTREC numbers to be used only in the event of chemical emergencies involving a spill, leak, fire, exposure or accident involving chemicals. SECTION 2: HAZARDOUS INGREDIENTS / IDENTITY INFORMATION NOTE: This material is purchased from a number of suppliers and distributed by Vishay Micro- Measurements. To ensure that you have the appropriate information, cross-reference the following data with the manufacturer’s label on the product you purchased. CAS NUMBER CHEMICAL IDENTITY % Methyl Cyanoacrylate Adhesive MC-100 (Chemence, Inc.) 137-05-3 Methyl 2-Cyanoacrylate 90-95 9011-14-7 Poly Methyl Methacrylate 5-10 123-31-9 Hydroquinone 0.1-0.5 Cyberbond APOLLO 2010 (Cyberbond, L.L.C.) 7085-85-0 Ethyl 2 Cyanoacrylate 80-90 9011-14-7 Poly Methyl Methacrylate 10-20 SI 120 Cyanoacrylate Adhesive (Adhesive Systems, Inc.) 7085-85-0 Ethyl Cyanoacrylate 80-95 9011-14-7 Poly (Methyl Methacrylate) 1-10 123-31-9 Hydroquinone 0.1-0.5 805-FRM011 M-Bond 200 Adhesive MSDS # MGM007P SECTION 3: HEALTH HAZARD DATA Routes of Entry: Inhalation: YES Skin: YES Ingestion: Accidental Health Hazards (Acute and Chronic): Bonds skin rapidly and strongly. Carcinogenicity: NTP: Not listed IARC Monographs: Not listed OSHA Regulated: Not listed Signs and Symptoms of Exposure: INHALATION: Vapor is irritating to nose and bronchial passages.
    [Show full text]
  • A Review of One-Step Fluorescent Cyanoacrylate Techniques
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Abertay Research Portal A review of one-step fluorescent cyanoacrylate techniques Vanessa Stewart, Paul Deacon, Kevin Farrugia This is the accepted manuscript © 2016 the Fingerprint Society which is published in final form in 2016 in Fingerprint Whorld. Stewart, V. Deacon, P. and Farrugia, K.J. 2016. A review of one- step fluorescent cyanoacrylate techniques. Fingerprint Whorld. 41(162). A review of one-step fluorescent cyanoacrylate techniques Vanessa Stewart, Paul Deacon, Kevin Farrugia* School of Science, Engineering & Technology, Division of Science, Abertay University, Bell Street, Dundee, DD1 1HG, UK * Corresponding Author: School of Science, Engineering & Technology Division of Science Abertay University Bell Street Dundee DD1 1HG United Kingdom tel: +44 (0) 1382 308689 [email protected] 1 Abstract A review of recent research in the use of one-step fluorescent cyanoacrylate techniques is presented. Advantages and disadvantages of such techniques in comparison to two-step processes are discussed. Further studies and new experimental data are presented to aid this review: three one-step cyanoacrylate products (Lumicyano, PolyCyano UV and PECA Multiband) containing a fluorescent dye were tested to evaluate their effectiveness in developing latent fingermarks on polyethylene bags by means of a pseudo operational trial. The results were compared to the traditional two-step process of cyanoacrylate fuming followed by staining with ethanol-based basic yellow 40 (BY40). The study was conducted using sequential treatments of an initial fuming cycle, a second cycle and finally BY40 staining. LumicyanoTM and PolyCyano UV performed similarly before BY40 staining, with both providing good contrast and visibility under fluorescence.
    [Show full text]
  • Chemical Bonds, Winter 2015
    Winter 2015 CHEMICAL BONDS THE UNIVERSITY OF TENNESSEE, KNOXVILLE DEPARTMENT OF CHEMISTRY Welcome New Faculty !!! Vol VI Issue No.1 Chemical Bonds is published biannually Contents by the University of Tennessee, Knoxville, Department of Chemistry Dr. Charles Feigerle Professor and Department Head 3 Department News Dr. Diane Schmidt 5 Faculty Highlights President, Chemistry Board of Visitors Dr. Rachel Rui 7 National Spotlight Writer/Editor/Photographer/Graphic Designer Pam Roach 9 Student Features Proofreader Address correspondence to the editor: The University of Tennessee, Knoxville Department of Chemistry The University of Tennessee 552 Buehler Hall 1420 Circle Dr. Knoxville, TN 37996-1600 Featured Group: Xue Research Group [email protected] (865) 974-8019 Visit the Department of Chemistry Website at www.chem.utk.edu Access this issue online by scanning the QR code below or go to https://www.chem.utk.edu/home/publications 11/16/15 A paper on the syntheses and characterization of tantalum alkyl imides and amide imides has been accepted for publication in Organometallics. Led to Seth Hunter, this work is a collaboration with Professor Michael Richmond of the University of North Texas. 9/18/15 A paper on magnetic transitions (zero-field splittings or ZFS) in iron porphyrin halides by inelastic neutron scattering (INS) and ab initio studies of the origins of ZFS has been accepted for publication in Inorganic Chemistry. Led by Shelby Stavretis, INS studies were conducted with Dr. Andrey Podlesnyak of Oak Ridge National Laboratory at Cold Neutron Chopper Spectrometer, Spallation Neutron Source. The work is also a collaboration with Dr. Mihail Atanasov, Institute of General and Inorganic Chemistry in the Bulgarian Academy of Sciences and Max Planck Institute (MPI) for Chemical Energy Conversion in Germany, and Dr.
    [Show full text]