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CHLOROPROCAINE

Product Name
CHLOROPROCAINE
CAS No.
133-16-4
Chemical Name
CHLOROPROCAINE
Synonyms
C07877;Halestyn;Piocaine;nescaine;nesacaine;Chlorprocaine;Chloroprocain;CHLOROPROCAINE;2-Chloroprocaine;SGVQMKDQDTWFEM-UHFFFAOYSA-N
CBNumber
CB4183345
Molecular Formula
C13H19ClN2O2
Formula Weight
270.76
MOL File
133-16-4.mol
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CHLOROPROCAINE Property

Melting point:
42°C
Boiling point:
402.6±35.0 °C(Predicted)
Density 
1.2020 (rough estimate)
refractive index 
1.5270 (estimate)
pka
9.14±0.25(Predicted)
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Safety

Hazardous Substances Data
133-16-4(Hazardous Substances Data)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0008904
Product name
CHLOROPROCAINE
Purity
95.00%
Packaging
5MG
Price
$504.25
Updated
2021/12/16
AvaChem
Product number
2816B
Product name
Chloroprocaine
Packaging
100mg
Price
$145
Updated
2021/12/16
AvaChem
Product number
2816B
Product name
Chloroprocaine
Packaging
1g
Price
$350
Updated
2021/12/16
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CHLOROPROCAINE Chemical Properties,Usage,Production

Description

Chloroprocaine (N,N′-diethylaminoethyl 4-amino-2-chlorobenzoate) is a very short-acting, amino ester-type local anesthetic used to provide regional anesthesia by infiltration as well as by peripheral and central nerve block, including lumbar and caudal epidural blocks. The presence of a chlorine atom ortho to the carbonyl of the ester function increases its rate of hydrolysis by plasma cholinesterase at least threefold compared to procaine and benzocaine. Thus, chloroprocaine may be used in maternal and neonatal patients with minimal placental passage of chloroprocaine. The lower plasma cholinesterase activity in the maternal epidural space must still have sufficient activity for degrading chloroprocaine and, thus, not allowing it to cross the placenta barrier. Like PABA, the hydrolysis product of chloroprocaine, 4-amino-2-chlorobenzoic acid, also inhibits the action of sulfonamides. Therefore, its use with sulfonamides should be avoided.

Uses

Chloroprocaine is an ester that is metabolised rapidly by ester hydrolysis, so its duration of action is short and potential for cardiac toxicity relatively low. It can be used as a preservative-free solution for spinal anaesthesia for surgical procedures up to 40 min in duration.

Uses

Anesthetic (local).

Definition

ChEBI: Procaine in which one of the hydrogens ortho- to the carboxylic acid group is substituted by chlorine. It is used as its monohydrochloride salt as a local anaesthetic, particularly for oral surgery. It has the advantage over lidocaine of const icting blood vessels, so reducing bleeding.

brand name

Nesacaine (Abraxis).

Biological Functions

Chloroprocaine hydrochloride (Nesacaine) is obtained from addition of a chlorine atom to procaine, which results in a compound of greater potency and less toxicity than procaine itself. This local anesthetic is hydrolyzed very rapidly by cholinesterase and therefore has a short plasma half-life. Because it is broken down rapidly, chloroprocaine is commonly used in obstetrics. It is believed that the small amount that might get to the fetus continues to be rapidly hydrolyzed, so there may be no residual effects on the neonate.

General Description

The 2 chloride substitution on the aromatic ring of chloroprocaineis an electron-withdrawing functional group. Thus, itpulls the electron density from the carbonyl carbon into thering. The carbonyl carbon is now a stronger electrophile andmore susceptible to ester hydrolysis. Therefore, chloroprocainehas a more rapid metabolism than procaine. The in vitroplasma half-life is approximately 25 seconds. The 2-chloro-4-aminobenzoic acid metabolite precludes this from being usedin patients allergic to PABA. The very short duration of actionmeans that this drug can be used in large doses for conductionblock (with rapid onset and short duration of action.).

Clinical Use

Chloroprocaine is used for cutaneous or mucous membraneinfiltration for surgical procedures, epidural anesthesia(without preservatives) and for peripheral conduction block.

CHLOROPROCAINE Preparation Products And Raw materials

Raw materials

Preparation Products

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CHLOROPROCAINE Suppliers

Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12335
Advantage
58
Dayang Chem (Hangzhou) Co.,Ltd.
Tel
571-88938639 +8617705817739
Fax
+86-571-88938652,+86-571- 88492614
Email
info@dycnchem.com
Country
China
ProdList
52849
Advantage
58
Career Henan Chemica Co
Tel
+86-0371-86658258 +8613203830695
Fax
0371-86658258
Email
laboratory@coreychem.com
Country
China
ProdList
30239
Advantage
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QUALITY CONTROL SOLUTIONS LTD.
Tel
0755-66853366; 13670046396
Email
ORDERS@QCSRM.COM
Country
China
ProdList
24342
Advantage
58
TargetMol Chemicals Inc.
Tel
4008200310
Email
marketing@tsbiochem.com
Country
China
ProdList
24644
Advantage
58
Shanghai Yifei Biotechnology Co. , Ltd.
Tel
021-65675885 18964387627
Email
customer_service@efebio.com
Country
China
ProdList
11974
Advantage
58
Tel
58896805
Email
7993601name@qq.com
Country
CHINA
ProdList
15620
Advantage
58
TargetMol Chemicals Inc.
Tel
+8613564774135
Email
zijue.cai@tsbiochem.com
Country
United States
ProdList
19885
Advantage
58
GIHI CHEMICALS CO.,LIMITED
Tel
+8618058761490
Email
info@gihichemicals.com
Country
China
ProdList
49978
Advantage
58
PT CHEM GROUP LIMITED
Tel
+86-85511178; +86-85511178;
Email
peter68@ptchemgroup.com
Country
China
ProdList
35425
Advantage
58

133-16-4, CHLOROPROCAINERelated Search:


  • CHLOROPROCAINE
  • 2-DIETHYLAMINOETHYL 4-AMINO-2-CHLORO-BENZOATE
  • 2-Chloroprocaine
  • 4-amino-2-chloro-benzoicaci2-(diethylamino)ethylester
  • Benzoic acid, 4-amino-2-chloro-, 2-(diethylamino)ethyl ester
  • Chloroprocain
  • Chlorprocaine
  • Halestyn
  • nesacaine
  • nescaine
  • Piocaine
  • CHLOROPROCAINE(2-CHLOROPROCAINE HYDROCHLORIDE)
  • C07877
  • SGVQMKDQDTWFEM-UHFFFAOYSA-N
  • 133-16-4