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Pralidoxime Chloride

Product Name
Pralidoxime Chloride
CAS No.
51-15-0
Chemical Name
Pralidoxime Chloride
Synonyms
PAM-CL;2-PAM-Cl;protopam;Pyraloxime;PAM CHLORIDE;2-PAM CHLORIDE;protopamchloride;Pyraloxime chloride;PRALIDOXIME CHLORIDE;Pralidoxome Chloride
CBNumber
CB8417130
Molecular Formula
C7H9ClN2O
Formula Weight
172.61
MOL File
51-15-0.mol
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Pralidoxime Chloride Property

Melting point:
230 °C (lit.)
Density 
1.3265 (rough estimate)
refractive index 
1.5430 (estimate)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Methanol (Slightly), Water (Sparingly)
pka
pKa 7.8-8 (Uncertain)
form 
Solid
color 
White to Off-White
Water Solubility 
65.5 g/100 mL (25 ºC)
Merck 
14,7703
BRN 
4163981
CAS DataBase Reference
51-15-0(CAS DataBase Reference)
EPA Substance Registry System
Pralidoxime chloride (51-15-0)
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Safety

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38-20/22
Safety Statements 
36-37/39-26
WGK Germany 
3
RTECS 
UU4200000
HS Code 
29333999
Toxicity
LD50 in rats (mg/kg): 96 i.v. (Fleisher); LD50 in rabbits (mg/kg): 95 i.v.; LD50 in mice (mg/kg): 115 i.v., 205 i.p., 4100 orally (Ellin, Wills)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
P9053
Product name
Pyridine-2-aldoxime methochloride
Packaging
5g
Price
$96.8
Updated
2024/03/01
Sigma-Aldrich
Product number
1553000
Product name
Pralidoxime chloride
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
200mg
Price
$400
Updated
2022/05/15
TCI Chemical
Product number
M0819
Product name
1-Methylpyridinium-2-aldoxime Chloride
Purity
>98.0%(HPLC)(T)
Packaging
25g
Price
$104
Updated
2024/03/01
Alfa Aesar
Product number
B23890
Product name
Pyridine-2-carboxaldoxime methochloride, 97%
Packaging
5g
Price
$35.65
Updated
2024/03/01
Alfa Aesar
Product number
B23890
Product name
Pyridine-2-carboxaldoxime methochloride, 97%
Packaging
25g
Price
$117.65
Updated
2024/03/01
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Pralidoxime Chloride Chemical Properties,Usage,Production

Chemical Properties

white to off-white adhering crystalline powder

Originator

Contrathion, Specia ,France,1961

Uses

vitamin B6, enzyme cofactor

Uses

This compound binds to inactivated acetylcholinesterases and is used to combat poisoning from organophosphates and nerve agents

Definition

ChEBI: Pralidoxime chloride is a pyridinium salt and an organic chloride salt. It has a role as a cholinesterase reactivator and a cholinergic drug. It contains a pralidoxime.

Manufacturing Process

As described in US Patent 3,123,613, the preparation of the intermediate product, 2-pyridinealdoxime methomethylsulfate, is as follows. 1 kg of 2pyridinealdoxime is dissolved in 6 liters of acetone and filtered until clear. 2 kg (2 equivalents) of freshly distilled dimethyl sulfate are added and the solution mixed. In about 30 minutes crystals start to appear, after which a cooling bath is used to keep the temperature at about 30° to 35°C until the reaction is nearly complete (about 2 hours).
The mixture is allowed to stand at room temperature overnight, the crystals filtered off and washed on a filter with acetone. The product is obtained as colorless needles, which melt at 111° to 112.5°C. The methylsulfate is not stable indefinitely. For preparation of pure chloride salt it is desirable to use methylsulfate which gives no titratable acidity with sodium hydroxide using bromophenol blue as indicator.
10 g of 2-pyridinealdoxime methomethylsulfate are then dissolved in 6 cc of concentrated hydrochloric acid, and 60 cc of isopropanol is added with stirring. Crystals appear almost instantly. After 2 hours standing at room temperature, the crystals are separated by filtration and washed with acetone. The product had a melting point of 227° to 228°C and the yield was 85%.
An alternative route is described in US Patent 3,155,674.
(A) Preparation of 1-Methyl-2-Picolinium Chloride: 98 ml of α-picoline is dissolved in 200 ml of methanol, cooled and 85 ml (at -68°C) of methyl chloride is added. The solution is charged to an autoclave, sealed and the nitrogen pressure of 300 psig is established. The mixture is heated at 120° to 130°C for 2 hours, cooled and opened. The resulting solution is then evaporated to dryness in vacuo, yielding a residue of 110 g. This residue is then dissolved in 50 ml of water and extracted with two 50 ml portions of ether. The aqueous phase is then diluted to 150 ml with water and an assay for ionic chloride is performed which indicates the presence of chloride ion equivalent to 721 mg/ml of l-methyl-2picolinium chloride.
(B) Preparation of 2-(Hydroxyiminomethyl)-1-Methyl Pyridinium Chloride: An aqueous solution of 15 ml of 1-methyl-2-picolinium chloride having a concentration of 477 mg/ml is covered with 50 ml of benzene in an atmosphere of nitrogen and cooled to below 10°C. An aqueous solution of sodium hydroxide is added dropwise and the mixture is stirred for 5 minutes and allowed to stratify. The aqueous phase is then drawn off and the benzenesolution is added slowly to a solution of 3 ml of nitrosyl chloride in 175 ml of benzene containing 0.5 ml of dimethyl formamide at about 10°C in an atmosphere of nitrogen with good agitation. The mixture is then stirred for 1.5 hours and then extracted with four 5 ml of portions of water. The aqueous extracts are then concentrated in vacuo, 30 ml of isopropanol is added and the concentration is repeated. 20 ml of isopropanol is then added to the concentrated mixture, and the mixture is cooled to room temperature and filtered, yielding 3.04 g of crude 2-(hydroxyiminomethyl)-1-methylpyridinium chloride, melting at 202° to 214°C with decomposition. The filtrate is then further concentrated to a 7 g residue which is crystallized from absolute alcohol and yields 0.9 g of 2-(hydroxyiminomethyl)-1-methyl pyridinium chloride melting at 221° to 225°C with decomposition.

brand name

Protopam Chloride (Baxter Healthcare); Protopam Chloride (Wyeth).

Therapeutic Function

Antidote (nerve gas)

General Description

Pralidoxime chloride, 2-formyl-1-methylpyridinium chloride oxime, 2-PAM chloride,or 2-pyridine aldoxime methyl chloride (Protopamchloride), is a white, nonhygroscopic, crystalline powderthat is soluble in water, 1 g in less than 1 mL.

Biochem/physiol Actions

The prototypical reactivator of acetylcholinesterase that has been inactivated by organophosphorus insecticides or nerve agents. It is now known that no reactivator is effective against a broad spectrum of organophosphorus agents.

Clinical Use

Pralidoxime chloride is used as an antidote for poisoningby parathion and related pesticides. It may be effectiveagainst some phosphates that have a quaternary nitrogen. Itis also an effective antagonist for some carbamates, such asneostigmine methylsulfate and pyridostigmine bromide.

Pralidoxime Chloride Preparation Products And Raw materials

Raw materials

Preparation Products

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Pralidoxime Chloride Suppliers

Chengdu Lisite Pharmaceutical Co., Ltd.
Tel
028-85918191
Email
hy@liarma.com
Country
China
ProdList
9
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94657
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44688
Advantage
61
Shanghai Longsheng chemical Co.,Ltd.
Tel
021-58099652-8005 13585536065
Fax
021-58099609
Email
bin.wu@shlschem.com
Country
China
ProdList
9809
Advantage
59
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42958
Advantage
64
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32321
Advantage
50
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18738
Advantage
57
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View Lastest Price from Pralidoxime Chloride manufacturers

Hebei Zhuanglai Chemical Trading Co Ltd
Product
Pralidoxime Chloride 51-15-0
Price
US $150.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
500kg
Release date
2024-11-21
Henan Suikang Pharmaceutical Co.,Ltd.
Product
Pyraloxime Methylchloride 51-15-0
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
99.0%
Supply Ability
1tons
Release date
2024-04-26
WUHAN FORTUNA CHEMICAL CO., LTD
Product
Pralidoxime Chloride 51-15-0
Price
US $0.00/KG
Min. Order
1KG
Purity
98.0%
Supply Ability
50kg/month
Release date
2023-01-09

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