TRIMETHYLACETIC ACID CHLORIDE
TRIMETHYLACETIC ACID CHLORIDE
Trimethylacetic acid chloride is used as a precursor in the preparation of various pharmaceutical and agrochemical products, including drugs, insecticides, and herbicides.
Trimethylacetic acid chloride is a highly reactive and toxic compound, used in organic synthesis for the production of pharmaceuticals, dyes, and other organic compounds.
Trimethylacetic acid chloride appears as a colorless to light yellow liquid with a pungent odor and is very toxic by inhalation, ingestion, or skin absorption.
CAS Number: 3282-30-2
EC Number: 221-921-6
Chemical Formula: C5H9ClO
Molar Mass: 120.58 g·mol−1
Synonyms: Pivaloyl chloride, 3282-30-2, Trimethylacetyl chloride, 2,2-DIMETHYLPROPANOYL CHLORIDE, Propanoyl chloride, 2,2-dimethyl-, Pivalyl chloride, 2,2-Dimethylpropionyl chloride, Pivalic acid chloride, Pivalolyl chloride, pivalic chloride, Neopentanoyl chloride, 2,2-dimethyl-propionyl chloride, JQ82J0O21T, 2,2,2-trimethylacetyl chloride, DTXSID4027529, 2,2-dimethylpropionic acid chloride, pivaloylchloride, Pivaloyl chlorid, pivaloylchlorid, UNII-JQ82J0O21T, Pvaloyl chlorde, PivCl, pivaloyl-chloride, 2,2, Dimethyl-propanoyl chloride, tBuCOCl, Piv-Cl, t-BuCOCl, EINECS 221-921-6, UN2438, PVCL, trimethylacetylchloride, trimethylacetyl choride, trimehtylacetyl chloride, trimethyl acetylchloride, Trimethylacetyl-chloride, t-butylcarbonyl chloride, trimethylacetoyl chloride, Trimethyl acetyl chloride, (CH3)3CCOCl, tert-butylcarbonyl chloride, EC 221-921-6, Acetyl chloride, trimethyl-, SCHEMBL1404, trimethylacetic acid chloride, 2,2-dimethylpropanoylchloride, 2,2-dimethylpropionylchloride, 2,2,2-trimethylacetylchloride, 2,2-Dimethyl-propionylchloride, Trimethylacetyl chloride, 99%, DTXCID907529, TERT-BUTYL CHLORO KETONE, 2,2-dimethyl propanoyl chloride, CHEMBL3183814, 2,2-dimethylpropionicacid cloride, STR00119, ZINC1534960, Tox21_200646, BBL011382, MFCD00000709, STL146483, 2,2-Dimethyl-propionic acid chloride, AKOS000121190, UN 2438, NCGC00248779-01, NCGC00258200-01, 1,1-DIMETHYLETHANECARBONYL CHLORIDE, CAS-3282-30-2, FT-0652320, P0677, Pivaloyl chloride, purum, >=98.0% (GC), EN300-19178, Trimethylacetyl chloride [UN2438] [Poison], A821441, J-523982, Q2017164, F2190-0014, 2,2-Dimethylpropanoyl chloride [ACD/IUPAC Name], 2,2, Dimethylpropanoylchlorid [German] [ACD/IUPAC Name], 221-921-6 [EINECS], 3282-30-2 [RN], Chlorure de 2,2-diméthylpropanoyle [French] [ACD/IUPAC Name], Pivaloyl chloride, PIVALYL CHLORIDE, Propanoyl chloride, 2,2-dimethyl- [ACD/Index Name], Trimethylacetyl chloride, [503-30-0] [RN], 1,3-Propylene oxide, 102382 [Beilstein], 15722-48-2 [RN], 2,2,2-Trimethylacetyl chloride, 2,2-Dimethyl-propionyl chloride, 2,2-Dimethylpropionyl Chloride, 2,2-Dimethylpropionyl chloride, Trimethylacetyl chloride, Acetyl chloride, trimethyl-, Cyclooxabutane, MFCD00005167 [MDL number], Neopentanoyl chloride, Oxetane [ACD/Index Name] [ACD/IUPAC Name] [Wiki], PI-44939, Pivalic acid chloride, Pivalolyl chloride, PivaloylChloride, RQ6825000, STR00119, tert-Valeryl chloride, Trimethylacetyl chloride [UN2438] [Poison], Trimethylacetylchloride, Trimethylene Oxide, UN 2438
Trimethylacetic acid chloride is a branched-chain acyl chloride.
Trimethylacetic acid chloride was first made by Aleksandr Butlerov in 1874 by reacting pivalic acid with phosphorus pentachloride.
Trimethylacetic acid chloride is used as an input in the manufacture of some drugs, insecticides and herbicides.
Trimethylacetic acid chloride is a reactive compound that is used in the synthesis of pharmaceuticals, dyes, and other organic compounds.
Trimethylacetic acid chloride can be used as a precursor to amides, which are important pharmacological agents.
Trimethylacetic acid chloride undergoes chemiluminescence when reacted with hydrogen fluoride and potassium dichromate in the presence of an amide.
This reaction mechanism can be used to detect small amounts of Trimethylacetic acid chloride in solution.
Trimethylacetic acid chloride has been shown to have anti-inflammatory effects in autoimmune diseases and has been investigated for use as a cox-2 inhibitor.
Trimethylacetic acid chloride, also known as Pivaloyl chloride, is a colorless and volatile liquid with a strong odor.
Trimethylacetic acid chloride is an alkylating reagent and is widely used in organic synthesis for the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.
Trimethylacetic acid chloride is also used in the manufacture of drugs, pesticides, and other compounds.
Trimethylacetic acid chloride is a colorless to light yellow liquid with a pungent odor.
Trimethylacetic acid chloride hydrolyses in the presence of water.
Trimethylacetic acid chloride is used in the production of pharmaceuticals and agrochemicals.
Trimethylacetic acid chloride is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 to < 10 tonnes per annum. Trimethylacetic acid chloride is used in formulation or re-packing, at industrial sites and in manufacturing. Trimethylacetic acid chloride is a natural product found in Rhodiola rosea with data available. Trimethylacetic acid chloride appears as colorless fuming liquid with a pungent odor. Trimethylacetic acid chloride is very toxic by inhalation, ingestion or skin absorption. Trimethylacetic acid chloride is fumes irritate the eyes and mucous membranes. Trimethylacetic acid chloride is corrosive to most metals and tissue. Trimethylacetic acid chloride is used as a precursor in the preparation of tert-butyl peroxypivalate, guttiferon A derivatives, which is potential for the treatment of malaria. Trimethylacetic acid chloride is used as a raw material in the production of synthetic acidamide medicament and phenol ester medicament. In addition to this, Trimethylacetic acid chloride is used for the synthesis of active pharmaceutical ingredients such as aminobenzylpenicilin, cephalexin, cefazolin, dipivefrin and dipivalyl epinephrine. Trimethylacetic acid chloride is also used in heavy polymerization, N-acylating agent for amines, Schiff bases, pyrrolidinones as well as an O-acylating agent for alcohols, lactones and saccharides. Trimethylacetic acid chloride market an overview: Trimethylacetic acid chloride is classified as a harmful chemical with many restrictions on Trimethylacetic acid chloride handling and storage. Trimethylacetic acid chloride is used as a building block in the pharmaceutical and agrochemical industry. In pharmaceutical industries, Trimethylacetic acid chloride serves as an important acylating reagent. Trimethylacetic acid chloride is a major raw material used in the synthesis of amides and lipids. Different important drugs that are manufactured using Trimethylacetic acid chloride are Benzylpenicillin, adrenaline, cefazolin, and other drugs. In agrochemical industries, Trimethylacetic acid chloride finds Trimethylacetic acid chloride application in pesticide intermediates production. The major product agrochemical obtained from Trimethylacetic acid chloride is ChloroTrimethylacetic acid chloride. In chemical industries, Trimethylacetic acid chlorides are used in the synthesis of ketones, amino groups, and anhydrides. Trimethylacetic acid chloride market dynamics: The global consumption of Trimethylacetic acid chlorides is mainly associated with the growth in pharmaceutical and agrochemical industries. Which are the major drivers for the growth of the Trimethylacetic acid chlorides market around the world. The global Trimethylacetic acid chloride market is consolidated to a few global and regional players only. Major players in global Trimethylacetic acid chloride markets are mainly from China and India. These countries are global leaders of agrochemical substances. The demand for agrochemicals in these regions is mainly accelerated due to the government's positive attitude towards agriculture. The government of India has launched initiatives like Pradhan Mantri Krishi Sinchai Yojana(PMKSY), which helps to support farmers in these regions. With these schemes, the government is targeting an increase in the country's revenue from agriculture sectors. This positive attitude in the development of the agriculture sector will boost the global Trimethylacetic acid chloride Market in these countries. The same strategy is followed by various other developing countries of Asia and other parts of the world. The fluctuating international currency has negative impacts on the Trimethylacetic acid chloride market. Trimethylacetic acid chloride high flammability and corrosiveness have also raised the safety concerns for the manufacturer's Transportation of Trimethylacetic acid chloride to involve high risk. These are some of the restraining factors for the growth of the Trimethylacetic acid chloride market. Trimethylacetic acid chloride market analysis: Agrochemical industries have grown significantly in the Asia Pacific region due to the rising demand for food crops in these regions. China and India are leading producers of the agrochemical, which is utilized in regional development in the agriculture sector. Thus overall consumption Trimethylacetic acid chlorides expected to witness significant growth in these regions. The global Trimethylacetic acid chloride market in China and India is experiencing higher growth due to several government inanities, which are encouraging the growth of agriculture in these regions. Besides agrochemical industries, pharmaceuticals and chemical industries have shown significant growth in Asia Pacific regions, which leverages the global Trimethylacetic acid chloride market. The pharmaceutical industries have been growing at higher single digits CAGR in Europe and America. Since the application of Trimethylacetic acid chlorides is associated with drug manufacturing, the global Trimethylacetic acid chlorides are expected to rise in these regions. The agriculture sector being the least contributing sector to the country`s GDP of the United States, contributes a very less to global Trimethylacetic acid chlorides market. The Latin American & Middle East & Africa markets for Trimethylacetic acid chloride will show stagnant growth in the forecast period due to limited growth in agrochemical and pharmaceutical industries in these regions. Trimethylacetic acid chloride Market Snapshot (2022 to 2032): The global Trimethylacetic acid chloride demand is anticipated to rise at a CAGR of 4.3% to 6% during the forecast period between 2022 and 2032. Rising applications of Trimethylacetic acid chloride across pharmaceutical and agrochemical industries are driving growth in the global Trimethylacetic acid chloride market. Trimethylacetic acid chloride, also called 2, 2- dimethyl propanol chloride, is a branded chain acyl chloride with a pungent odor. Trimethylacetic acid chloride is being increasingly used as a building block in agrochemical, pharmaceutical, and refining chemicals industries. Over the years, Trimethylacetic acid chloride has become a commonly used intermediate for the production of agricultural chemicals like insecticides, herbicides, pesticides, pharmaceutical compounds, and in peroxy esters manufacturing. The rapid expansion of the pharmaceutical industry triggered by the increasing prevalence of various chronic and infectious diseases, growing health awareness, and increasing spending on medicines is expected to push the demand for Trimethylacetic acid chloride during the forecast period. Trimethylacetic acid chloride is being extensively used to manufacture pharmaceutical products such as DPE, cefazolin, dipivefrin, aminobenzylpenicilin, cephalexin, and digitally epinephrine. Driving Demand in Trimethylacetic acid chloride Market: The rapid growth of end-use industries such as chemical, agrochemical, and pharmaceutical is a major factor driving the demand for Trimethylacetic acid chloride. Trimethylacetic acid chloride has become an ideal intermediate candidate for manufacturing a wide range of pharmaceutical and agrochemical products. Factors such as a surge in diseases worldwide and increasing healthcare spending have ignited the growth of the pharmaceutical industry worldwide. People are spending large amounts on pharmaceutical drugs. As many of these pharmaceuticals are manufactured by using Trimethylacetic acid chloride as an intermediate, the rising dale for these products will eventually push the demand for Trimethylacetic acid chloride during the forecast period. Similarly, rising concerns about food insecurity are prompting farmers to use agrochemicals like herbicides, fertilizers, pesticides, etc. According to the Food and Agriculture Organization (FAO) of the United Nations, globally, hunger levels remained alarmingly high during 2021 with around 193 million people facing acute food insecurity. This is acting as a catalyst for the growth of the Trimethylacetic acid chloride market and the trend is likely to continue during the forecast period. Challenges Faced by the Trimethylacetic acid chloride Industry: Despite multiple applications of Trimethylacetic acid chloride, there are certain factors that are limiting the growth of the Trimethylacetic acid chloride industry. Some of these factors include the presence of stringent regulations pertaining to the use of insecticides and pesticides, the hazardous nature of Trimethylacetic acid chloride, and the availability of various alternative pharmaceutical and pesticide intermediates. Various countries are introducing regulations on the excessive use of insecticides and pesticides as they are harmful to humans, animals, and the environment. This in turn is creating major challenges for manufacturers of Trimethylacetic acid chloride. Scientific Research Applications of Trimethylacetic acid chloride: Trimethylacetic acid chloride is used in a variety of scientific research applications, such as the synthesis of peptides, the synthesis of heterocyclic compounds, and the synthesis of amines. Trimethylacetic acid chloride is also used in the synthesis of polymers, such as polystyrene and polyethylene. In addition, Trimethylacetic acid chloride is used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Uses of Trimethylacetic acid chloride: Trimethylacetic acid chloride is used as a precursor in the preparation of tert-butyl peroxypivalate, guttiferon A derivatives, which is potential for the treatment of malaria. Trimethylacetic acid chloride is used as a raw material in the production of synthetic acidamide medicament and phenol ester medicament. In addition to this, Trimethylacetic acid chloride is used for the synthesis of active pharmaceutical ingredients such as aminobenzylpenicilin, cephalexin, cefazolin, dipivefrin and dipivalyl epinephrine. Trimethylacetic acid chloride is also used in heavy polymerization, N-acylating agent for amines, Schiff bases, pyrrolidinones as well as an O-acylating agent for alcohols, lactones and saccharides. Trimethylacetic acid chloride is used as a chemical intermediate. Trimethylacetic acid chloride is used as a precursor in the preparation of tert-butyl peroxypivalate, guttiferon A derivatives, which is potential for the treatment of malaria. Trimethylacetic acid chloride is used as a raw material in the production of synthetic acidamide medicament and phenol ester medicament. In addition to this, Trimethylacetic acid chloride is used for the synthesis of active pharmaceutical ingredients such as aminobenzylpenicilin, cephalexin, cefazolin, dipivefrin and dipivalyl epinephrine. Trimethylacetic acid chloride is also used in heavy polymerization, N-acylating agent for amines, Schiff bases, pyrrolidinones as well as an O-acylating agent for alcohols, lactones and saccharides. Uses at industrial sites: Trimethylacetic acid chloride has an industrial use resulting in manufacture of another substance (use of intermediates). Trimethylacetic acid chloride is used for the manufacture of: chemicals. Release to the environment of Trimethylacetic acid chloride can occur from industrial use: as an intermediate step in further manufacturing of another substance (use of intermediates). Industry Uses: Intermediate Intermediates General Manufacturing Information of Trimethylacetic acid chloride: Industry Processing Sectors: All Other Basic Organic Chemical Manufacturing Pesticide, Fertilizer, and Other Agricultural Chemical Manufacturing Pharmaceutical and Medicine Manufacturing Synthesis Method of Trimethylacetic acid chloride: Trimethylacetic acid chloride is synthesized from trimethylacetic acid and thionyl chloride. The reaction is carried out in a sealed tube or flask at a temperature of 40-60°C. The reaction is exothermic and the reaction is complete in about 2 hours. The yield of the reaction is usually in the range of 75-95%. Chemical Structure of Trimethylacetic acid chloride: A chemical structure of a molecule includes the arrangement of atoms and the chemical bonds that hold the atoms together. The Trimethylacetic acid chloride molecule contains a total of 15 bond(s). There are 6 non-H bond(s), 1 multiple bond(s), 1 rotatable bond(s), 1 double bond(s) and 1 acyl halogenide(s) (aliphatic). The 2D chemical structure image of Trimethylacetic acid chloride is also called skeletal formula, which is the standard notation for organic molecules. The carbon atoms in the chemical structure of Trimethylacetic acid chloride are implied to be located at the corner(s) and hydrogen atoms attached to carbon atoms are not indicated – each carbon atom is considered to be associated with enough hydrogen atoms to provide the carbon atom with four bonds. The 3D chemical structure image of Trimethylacetic acid chloride is based on the ball-and-stick model which displays both the three-dimensional position of the atoms and the bonds between them. The radius of the spheres is therefore smaller than the rod lengths in order to provide a clearer view of the atoms and bonds throughout the chemical structure model of Trimethylacetic acid chloride. Reactivity Profile of Trimethylacetic acid chloride: Trimethylacetic acid chloride is acidic. Incompatible with bases (including amines), strong oxidizing agents, and alcohols. May react vigorously or explosively if mixed with diisopropyl ether or other ethers in the presence of trace amounts of metal salts. Handling and Storage of Trimethylacetic acid chloride: Nonfire Spill Response: ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area. All equipment used when handling Trimethylacetic acid chloride must be grounded. Do not touch or walk through spilled material. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. A vapor-suppressing foam may be used to reduce vapors. SMALL SPILL: Absorb with earth, sand or other non-combustible material and transfer to containers for later disposal. Use clean, non-sparking tools to collect absorbed material. LARGE SPILL: Dike far ahead of liquid spill for later disposal. Water spray may reduce vapor, but may not prevent ignition in closed spaces. First Aid Measures of Trimethylacetic acid chloride: Call 911 or emergency medical service. Ensure that medical personnel are aware of Trimethylacetic acid chloride(s) involved and take precautions to protect themselves. Move victim to fresh air if it can be done safely. Give artificial respiration if victim is not breathing. Do not perform mouth-to-mouth resuscitation if victim ingested or inhaled Trimethylacetic acid chloride; wash face and mouth before giving artificial respiration. Use a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. Wash skin with soap and water. In case of burns, immediately cool affected skin for as long as possible with cold water. Do not remove clothing if adhering to skin. Keep victim calm and warm. Effects of exposure (inhalation, ingestion or skin contact) to substance may be delayed. Fire Fighting of Trimethylacetic acid chloride: The majority of these products have a very low flash point. Use of water spray when fighting fire may be inefficient. Methanol (UN1230) will burn with an invisible flame. Use an alternate method of detection (thermal camera, broom handle, etc.). SMALL FIRE: Dry chemical, CO2, water spray or alcohol-resistant foam. LARGE FIRE: Water spray, fog or alcohol-resistant foam. If it can be done safely, move undamaged containers away from the area around the fire. Dike runoff from fire control for later disposal. Avoid aiming straight or solid streams directly onto the product. FIRE INVOLVING TANKS OR CAR/TRAILER LOADS: Fight fire from maximum distance or use unmanned master stream devices or monitor nozzles. Cool containers with flooding quantities of water until well after fire is out. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire. For massive fire, use unmanned master stream devices or monitor nozzles. If this is impossible, withdraw from area and let fire burn. Accidental Release Measures of Trimethylacetic acid chloride: Isolation and Evacuation: IMMEDIATE PRECAUTIONARY MEASURE: Isolate spill or leak area for at least 50 meters (150 feet) in all directions. FIRE: If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions. Identifiers of Trimethylacetic acid chloride: CAS Number: 3282-30-2 Beilstein Reference: 102382 ChEMBL: ChEMBL3183814 ChemSpider: 56272 ECHA InfoCard: 100.019.929 EC Number: 221-921-6 PubChem CID: 62493 UNII: JQ82J0O21T UN number: 2438 CompTox Dashboard (EPA): DTXSID4027529 InChI: InChI=1S/C5H9ClO/c1-5(2,3)4(6)7/h1-3H3 Key: JVSFQJZRHXAUGT-UHFFFAOYSA-N SMILES: CC(C)(C)C(=O)Cl Synonym(s): Trimethylacetic acid chloride, Trimethylacetyl chloride Linear Formula: (CH3)3CCOCl CAS Number: 3282-30-2 Molecular Weight: 120.58 Beilstein: 385668 EC Number: 221-921-6 MDL number: MFCD00000709 PubChem Substance ID: 24900440 NACRES: NA.22 CAS number: 3282-30-2 EC number: 221-921-6 Hill Formula: C₅H₉ClO Chemical formula: (CH₃)₃CCOCl Molar Mass: 120.58 g/mol HS Code: 2915 90 70 EC / List no.: 221-921-6 CAS no.: 3282-30-2 Mol. formula: C5H9ClO Product Number: P0677 Purity / Analysis Method: >98.0%(T)
Molecular Formula / Molecular Weight: C5H9ClO = 120.58
Physical State (20 deg.C): Liquid
Storage Temperature: 0-10°C
Store Under Inert Gas: Store under inert gas
Condition to Avoid: Moisture Sensitive,Heat Sensitive
CAS RN: 3282-30-2
Reaxys Registry Number: 385668
PubChem Substance ID: 125310048
SDBS (AIST Spectral DB): 2154
MDL Number: MFCD00000709
Properties of Trimethylacetic acid chloride:
Chemical formula: C5H9ClO
Molar mass: 120.58 g·mol−1
Density: 0.985
Melting point: −57 °C (−71 °F; 216 K)
Boiling point: 105.5 °C (221.9 °F; 378.6 K)
Refractive index (nD): 1.412
Boiling point: 105 °C (1013 hPa)
Density: 0.98 g/cm3 (20 °C)
Explosion limit: 1.9 – 7.4 %(V)
Flash point: 13 °C
Ignition temperature: 455 °C
Melting Point: 87 – 88 °C
Vapor pressure: 38.59 hPa (20 °C)
Vapor density: >1 (vs air)
Quality Level: 200
Vapor pressure: 36 mmHg ( 20 °C)
Assay: 99%
Refractive index: n20/D 1.412 (lit.)
bp: 105-106 °C (lit.)
Density: 0.979 g/mL at 25 °C (lit.)
SMILES string: CC(C)(C)C(Cl)=O
InChI: 1S/C5H9ClO/c1-5(2,3)4(6)7/h1-3H3
InChI key: JVSFQJZRHXAUGT-UHFFFAOYSA-N
Molecular Weight: 120.58
XLogP3-AA: 2.2
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 1
Exact Mass: 120.0341926
Monoisotopic Mass: 120.0341926
Topological Polar Surface Area: 17.1 Ų
Heavy Atom Count: 7
Complexity: 80.6
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Specifications of Trimethylacetic acid chloride:
Assay (morpholine method): ≥ 98.0 %
Density (d 20 °C/ 4 °C): 0.979 – 0.982
Identity (IR): passes test
Related Products of Trimethylacetic acid chloride:
1,1-Dimethoxybutane
(E)-6,6-Dimethyl-2-hept-1-en-4-yn-1-amine
2,2-dimethoxybutane
Dimethyl trans-3-Hexenedioate
Dimethyl Hydroxyaspartate, Mixture of Diastereomers
Names of Trimethylacetic acid chloride:
Regulatory process names:
Trimethylacetic acid chloride
Trimethylacetic acid chloride
Trimethylacetic acid chloride
TRIMETHYLACETYL CHLORIDE
Directive, Annex II – RID
CAS names:
Propanoyl chloride
2,2-dimethyl-
IUPAC names:
2,2-Dimethylpropanoyl chloride
2,2-dimethylpropanoyl chloride
2,2-dimethylpropanoylchloride
2,2-dimethylpropionic acid chloride
Trimethylacetic acid chloride
Preferred IUPAC name:
2,2-Dimethylpropanoyl chloride
Trade names:
1,1-Dimethylethanecarbonyl chloride
2,2-Dimethylpropanoyl chloride
2,2-Dimethylpropionic acid chloride
2,2-Dimethylpropionyl chloride
Neopentanoyl chloride
Pivalic acid chloride
Pivalolyl chloride
Trimethylacetic acid chloride
Trimethylacetic acid chloride (6CI, 7CI, 8CI)
Pivaloylchlorid
Pivalyl chloride
Propanoyl chloride, 2,2-dimethyl-
Propanoyl chloride, 2,2-dimethyl- (9CI)
tert-Butyl chloro ketone
tert-Butylcarbonyl chloride
Trimethylacetyl chloride
Other names:
Trimethylacetyl chloride
Trimethylacetic acid chloride
Pivalyl chloride
neopentanoylchloride
Other identifier:
3282-30-2