PIVALOYL CHLORIDE

Pivaloyl chloride, also known as Trimethylacetic acid chloride, is a colorless and volatile liquid with a strong odor. 
Pivaloyl chloride is a colorless to light yellow liquid with a pungent odor. 
Pivaloyl chloride (PIVCL) is used in the production of pharmaceuticals and agrochemicals.

CAS Number: 3282-30-2
EC Number: 221-921-6
Chemical Formula: C5H9ClO
Molar Mass: 120.58 g·mol−1

Pivaloyl chloride is a branched-chain acyl chloride.
Pivaloyl chloride was first made by Aleksandr Butlerov in 1874 by reacting pivalic acid with phosphorus pentachloride.

Pivaloyl chloride is used as an input in the manufacture of some drugs, insecticides and herbicides.

Pivaloyl chloride (PC) is a reactive compound that is used in the synthesis of pharmaceuticals, dyes, and other organic compounds. 
Pivaloyl chloride can be used as a precursor to amides, which are important pharmacological agents. 

PC 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 PC in solution. 
PC has been shown to have anti-inflammatory effects in autoimmune diseases and has been investigated for use as a cox-2 inhibitor.

Pivaloyl chloride, also known as Trimethylacetic acid chloride, is a colorless and volatile liquid with a strong odor. 
Pivaloyl chloride is an alkylating reagent and is widely used in organic synthesis for the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. 
Pivaloyl chloride is also used in the manufacture of drugs, pesticides, and other compounds.

Pivaloyl chloride is a colorless to light yellow liquid with a pungent odor. 
Pivaloyl chloride hydrolyses in the presence of water.

Pivaloyl chloride (PIVCL) is used in the production of pharmaceuticals and agrochemicals.

Pivaloyl 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.
Pivaloyl chloride is used in formulation or re-packing, at industrial sites and in manufacturing.

Pivaloyl chloride is a natural product found in Rhodiola rosea with data available.
Pivaloyl chloride appears as colorless fuming liquid with a pungent odor. 

Pivaloyl chloride is very toxic by inhalation, ingestion or skin absorption. 
Pivaloyl chloride is fumes irritate the eyes and mucous membranes. 
Pivaloyl chloride is corrosive to most metals and tissue.

Pivaloyl chloride is used as a precursor in the preparation of tert-butyl peroxypivalate, guttiferon A derivatives, which is potential for the treatment of malaria. 
Pivaloyl chloride is used as a raw material in the production of synthetic acidamide medicament and phenol ester medicament. 
In addition to this, Pivaloyl chloride is used for the synthesis of active pharmaceutical ingredients such as aminobenzylpenicilin, cephalexin, cefazolin, dipivefrin and dipivalyl epinephrine. 

Pivaloyl 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.

Pivaloyl chloride market an overview:
Pivaloyl chloride is classified as a harmful chemical with many restrictions on Pivaloyl chloride handling and storage. 
Pivaloyl chloride is used as a building block in the pharmaceutical and agrochemical industry. 

In pharmaceutical industries, Pivaloyl chloride serves as an important acylating reagent. 
Pivaloyl chloride is a major raw material used in the synthesis of amides and lipids.

Different important drugs that are manufactured using Pivaloyl chloride are Benzylpenicillin, adrenaline, cefazolin, and other drugs. 
In agrochemical industries, Pivaloyl chloride finds Pivaloyl chloride application in pesticide intermediates production. 
The major product agrochemical obtained from Pivaloyl chloride is Chloropivaloyl chloride.

In chemical industries, Pivaloyl chlorides are used in the synthesis of ketones, amino groups, and anhydrides.

Pivaloyl chloride market dynamics:
The global consumption of Pivaloyl chlorides is mainly associated with the growth in pharmaceutical and agrochemical industries. 
Which are the major drivers for the growth of the Pivaloyl chlorides market around the world. 

The global Pivaloyl chloride market is consolidated to a few global and regional players only. 
Major players in global Pivaloyl 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 Pivaloyl 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 Pivaloyl chloride market. 
Pivaloyl chloride high flammability and corrosiveness have also raised the safety concerns for the manufacturer's Transportation of Pivaloyl chloride to involve high risk. 
These are some of the restraining factors for the growth of the Pivaloyl chloride market.

Pivaloyl 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 Pivaloyl chlorides expected to witness significant growth in these regions.

The global Pivaloyl 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 Pivaloyl chloride market.

The pharmaceutical industries have been growing at higher single digits CAGR in Europe and America. 
Since the application of Pivaloyl chlorides is associated with drug manufacturing, the global Pivaloyl 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 Pivaloyl chlorides market.

The Latin American & Middle East & Africa markets for Pivaloyl chloride will show stagnant growth in the forecast period due to limited growth in agrochemical and pharmaceutical industries in these regions.

Pivaloyl Chloride Market Snapshot (2022 to 2032):
The global pivaloyl 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 pivaloyl chloride across pharmaceutical and agrochemical industries are driving growth in the global pivaloyl chloride market.

Pivaloyl Chloride, also called 2, 2- dimethyl propanol chloride, is a branded chain acyl chloride with a pungent odor. 
Pivaloyl chloride is being increasingly used as a building block in agrochemical, pharmaceutical, and refining chemicals industries.

Over the years, pivaloyl 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 pivaloyl chloride during the forecast period.
Pivaloyl chloride is being extensively used to manufacture pharmaceutical products such as DPE, cefazolin, dipivefrin, aminobenzylpenicilin, cephalexin, and digitally epinephrine.

Driving Demand in Pivaloyl Chloride Market:
The rapid growth of end-use industries such as chemical, agrochemical, and pharmaceutical is a major factor driving the demand for pivaloyl chloride.

Pivaloyl 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 pivaloyl chloride as an intermediate, the rising dale for these products will eventually push the demand for pivaloyl 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 pivaloyl chloride market and the trend is likely to continue during the forecast period.

Challenges Faced by the Pivaloyl Chloride Industry:
Despite multiple applications of pivaloyl chloride, there are certain factors that are limiting the growth of the pivaloyl chloride industry. 
Some of these factors include the presence of stringent regulations pertaining to the use of insecticides and pesticides, the hazardous nature of pivaloyl 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 pivaloyl chloride.

Scientific Research Applications of Pivaloyl chloride:
Pivaloyl 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. 
Pivaloyl chloride is also used in the synthesis of polymers, such as polystyrene and polyethylene. 
In addition, Pivaloyl chloride is used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.

Uses of Pivaloyl chloride:
Pivaloyl chloride is used as a precursor in the preparation of tert-butyl peroxypivalate, guttiferon A derivatives, which is potential for the treatment of malaria. 
Pivaloyl chloride is used as a raw material in the production of synthetic acidamide medicament and phenol ester medicament. 

In addition to this, Pivaloyl chloride is used for the synthesis of active pharmaceutical ingredients such as aminobenzylpenicilin, cephalexin, cefazolin, dipivefrin and dipivalyl epinephrine. 
Pivaloyl 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.

Pivaloyl chloride is used as a chemical intermediate.
Pivaloyl chloride is used as a precursor in the preparation of tert-butyl peroxypivalate, guttiferon A derivatives, which is potential for the treatment of malaria. 

Pivaloyl chloride is used as a raw material in the production of synthetic acidamide medicament and phenol ester medicament. 
In addition to this, Pivaloyl chloride is used for the synthesis of active pharmaceutical ingredients such as aminobenzylpenicilin, cephalexin, cefazolin, dipivefrin and dipivalyl epinephrine. 

Pivaloyl 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:
Pivaloyl chloride has an industrial use resulting in manufacture of another substance (use of intermediates).
Pivaloyl chloride is used for the manufacture of: chemicals.
Release to the environment of Pivaloyl 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 Pivaloyl chloride:

Industry Processing Sectors:
All Other Basic Organic Chemical Manufacturing
Pesticide, Fertilizer, and Other Agricultural Chemical Manufacturing
Pharmaceutical and Medicine Manufacturing

Synthesis Method of Pivaloyl chloride:
Pivaloyl 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 Pivaloyl chloride:
A chemical structure of a molecule includes the arrangement of atoms and the chemical bonds that hold the atoms together. 
The Pivaloyl 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 Pivaloyl chloride is also called skeletal formula, which is the standard notation for organic molecules. 
The carbon atoms in the chemical structure of Pivaloyl 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 Pivaloyl 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 Pivaloyl chloride.

Reactivity Profile of Pivaloyl chloride:
Pivaloyl 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 Pivaloyl chloride:

Nonfire Spill Response:
ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area. 
All equipment used when handling Pivaloyl 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 Pivaloyl chloride:
Call 911 or emergency medical service. 
Ensure that medical personnel are aware of Pivaloyl 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 Pivaloyl 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 Pivaloyl 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 Pivaloyl 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 Pivaloyl 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): Pivaloyl 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 Pivaloyl 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 Pivaloyl chloride:
Assay (morpholine method): ≥ 98.0 %
Density (d 20 °C/ 4 °C): 0.979 - 0.982
Identity (IR): passes test

Related Products of Pivaloyl 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 Pivaloyl chloride:

Regulatory process names:
Pivaloyl chloride
Pivaloyl chloride
pivaloyl 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
Pivaloyl 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
pivaloyl chloride
Pivaloyl 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
Pivaloyl chloride
Pivalyl chloride
neopentanoylchloride

Other identifier:
3282-30-2

Synonyms of Pivaloyl chloride:
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