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Oxalyl chloride

CAS No.
79-37-8
Chemical Name:
Oxalyl chloride
Synonyms
OXALYL DICHLORIDE;Oxalyl;OC;formyl chloride;Oxalic dichloride;COX;ETHANEDIOYL DICHLORIDE;Oxalic chloride;Oxaloyl chloride;Oxalyl chloride solution 2.0 M in methylene chloride
CBNumber:
CB7854408
Molecular Formula:
C2Cl2O2
Molecular Weight:
126.93
MDL Number:
MFCD00000704
MOL File:
79-37-8.mol
MSDS File:
SDS
Last updated:2024-11-06 10:05:12

Oxalyl chloride Properties

Melting point -10--8 °C (lit.)
Boiling point 62-65 °C (lit.)
Density 1.5 g/mL at 20 °C (lit.)
vapor density 4.4 (vs air)
vapor pressure 150 mm Hg ( 20 °C)
refractive index n20/D 1.429(lit.)
Flash point 176-178°C
storage temp. Store Cold
solubility Chloroform (Soluble), Ethyl Acetate
form Liquid
color APHA: 0-150
Odor penetrating odor
Water Solubility reacts
Decomposition 176-178 ºC
Sensitive Moisture Sensitive
Merck 14,6914
BRN 1361988
Dielectric constant 3.5(21℃)
Exposure limits ACGIH: TWA 50 ppm
OSHA: TWA 25 ppm; STEL 125 ppm
NIOSH: IDLH 2300 ppm
Stability Stable. Incompatible with bases, alcohols, steel, oxidizing agents, alkali metals. Moisture sensitive. Reacts violently with water, liberating toxic gas.
InChIKey CTSLXHKWHWQRSH-UHFFFAOYSA-N
CAS DataBase Reference 79-37-8(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII R4Y96317DW
NIST Chemistry Reference Oxalyl chloride(79-37-8)
EPA Substance Registry System Ethanedioyl dichloride (79-37-8)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS05,GHS06
Signal word  Danger
Hazard statements  H260-H301+H331-H314
Precautionary statements  P223-P231+P232-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
Hazard Codes  C,T
Risk Statements  14-20-29-34-40-23/24/25-37-35-23
Safety Statements  26-36/37/39-43-45-8-24/25-23-27
RIDADR  UN 2927 6.1/PG 2
WGK Germany  2
RTECS  KI2950000
9-19-21
Hazard Note  Toxic/Corrosive/Store Cold/Lacrymatory
TSCA  Yes
HazardClass  8
PackingGroup  II
HS Code  29171990
NFPA 704
1
3 2
W

Oxalyl chloride price More Price(41)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 221015 Oxalyl chloride ReagentPlus , ≥99% 79-37-8 5g $27.8 2024-03-01 Buy
Sigma-Aldrich 221015 Oxalyl chloride ReagentPlus , ≥99% 79-37-8 10kg $2040 2024-03-01 Buy
TCI Chemical O0082 Oxalyl Chloride >98.0%(GC)(T) 79-37-8 25g $28 2024-03-01 Buy
TCI Chemical O0082 Oxalyl Chloride >98.0%(GC)(T) 79-37-8 100g $62 2024-03-01 Buy
Alfa Aesar A18012 Oxalyl chloride, 98% 79-37-8 50g $45.9 2023-06-20 Buy
Product number Packaging Price Buy
221015 5g $27.8 Buy
221015 10kg $2040 Buy
O0082 25g $28 Buy
O0082 100g $62 Buy
A18012 50g $45.9 Buy

Oxalyl chloride Chemical Properties,Uses,Production

Chemical Properties

colourless liquid with a pungent odour

Uses

Oxalyl Chloride is used in the preparation of cardiolipin analogs which induce peroxidase activity by Cytochrome C. It is also used in the preparation of fluorescent indicators for cytosolic calcium.

Production Methods

Oxalyl Chloride is produced by the reaction of anhydrous oxalic acid and phosphorus pentachloride.

Preparation

Oxalyl chloride was first prepared in 1892 by the French chemist Adrien Fauconnier, who reacted diethyl oxalate with phosphorus pentachloride. Oxalyl chloride is also produced commercially from ethylene carbonate. Photochlorination gives the tetrachloride, which is subsequently degraded:
C2H4O2CO + 4 Cl2 → C2Cl4O2CO + 4 HCl
C2Cl4O2CO → C2O2Cl2 + COCl2

Application

Oxalyl chloride is used in organic synthesis. It may be used in the following processes:
Unncatalyzed reaction of silyl ketene acetals with oxalyl chloride yeilds symmetrical pulvinic acids.
Catalytic syntheses of N-heterocyclic ynones and ynediones by in situ activation of carboxylic acids with oxalyl chloride.
Oxalyl chloride was reportedly used in the first synthesis of dioxane tetraketone.
Preparation of Mosher′s acid chloride by reacting with Mosher′s acid in the presence of DMF.
Activation of dimethyl sulfoxide for use in the oxidation of long-chain alcohols to carbonyls.
Activation of α-keto carboxylic acids and N-heterocyclic carboxylic acids for alkynylation to form ynediones and N-heterocyclic ynones, respectively.

Reactions

Oxalyl Chloride vigorously reacts with water, alcohols, and amines, and is employed for the synthesis of agrochemicals, pharmaceuticals, and fine chemicals.

General Description

Oxalyl chloride is a commonly used chlorinating reagent that can be prepared by the reaction of oxalic acid and phosphorus pentachloride.

Health Hazard

Oxalyl chloride is a corrosive respiratory irritant and lachrymator. The vapors will attack the skin, eyes and especially the mucous membranes of the nose and throat and respiratory system. This material should be used only in a well ventilated area.

Fire Hazard

Extinguish with dry powder or carbon dioxide. Do not use water. Oxalyl chloride decomposes upon contact with water to produce toxic and corrosive fumes. When heated to decomposition, product emits toxic fumes.

Chemical Reactivity

Oxalyl chloride is sensitive to temperatures below -10° and above 40°C. It reacts vigorously with water and hydroxyl compounds.

Safety Profile

Poison. Violently decomposed by water and alcohol. Severe irritant to skin, eyes, respiratory tract. Explodeson contact with dimethyl sulfoxide. Forms shock-sensitive explosive mixtures with potassium or with K-Na alloy. Will react with water or steam to

Waste Disposal

Carefully mix acidic compound with dry sodium bicarbonate. Dilute slowly with water and wash down the drain with copious amounts of water.

Global( 519)Suppliers
Supplier Tel Email Country ProdList Advantage
Ningxia Jinhua Chemical Co.,Ltd
025-52279164 info@nxjhchem.com China 79 58
Hebei Weibang Biotechnology Co., Ltd
+8615531157085 abby@weibangbio.com China 8810 58
Hebei Mojin Biotechnology Co., Ltd
+86 13288715578 +8613288715578 sales@hbmojin.com China 12839 58
Hebei Yanxi Chemical Co., Ltd.
+8617531190177 peter@yan-xi.com China 5857 58
Hebei Chuanghai Biotechnology Co,.LTD
+86-13131129325 sales1@chuanghaibio.com China 5892 58
Hebei Kangcang new material Technology Co., LTD
+8615713292910 Nancy@kangcang.com.cn China 341 58
Springchem New Material Technology Co.,Limited
+86-021-62885108 +8613917661608 info@spring-chem.com China 2068 57
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806 sales@capot.com China 29791 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21634 55
Shanghai Time Chemicals CO., Ltd.
+86-021-57951555 +8617317452075 jack.li@time-chemicals.com China 1803 55

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View Lastest Price from Oxalyl chloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Oxalyl chloride pictures 2024-11-04 Oxalyl chloride
79-37-8
US $1.00 / PCS 1PCS 99% 100mt Hebei Weibang Biotechnology Co., Ltd
Oxalyl chloride pictures 2024-10-25 Oxalyl chloride
79-37-8
US $0.00 / kg 1kg 0.99 20tons Hebei Yanxi Chemical Co., Ltd.
Oxalyl chloride pictures 2024-10-11 Oxalyl chloride
79-37-8
US $10.60 / KG 1KG 98% 5000kg Hebei Chuanghai Biotechnology Co,.LTD
  • Oxalyl chloride pictures
  • Oxalyl chloride
    79-37-8
  • US $1.00 / PCS
  • 99%
  • Hebei Weibang Biotechnology Co., Ltd
  • Oxalyl chloride pictures
  • Oxalyl chloride
    79-37-8
  • US $10.60 / KG
  • 98%
  • Hebei Chuanghai Biotechnology Co,.LTD
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