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543-20-4 Usage

Uses

It is employed in the synthesis of biseugenyl succinate and bis(4-maleimidephenyl) succinate. It is also used as used as an important raw material and intermediate in pharmaceuticals, organic synthesis, agrochemicals and dye stuffs. It is also applied as hydrolytic reagent for the determination of water.

Check Digit Verification of cas no

The CAS Registry Mumber 543-20-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 543-20:
(5*5)+(4*4)+(3*3)+(2*2)+(1*0)=54
54 % 10 = 4
So 543-20-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H4Cl2O2/c5-3(7)1-2-4(6)8/h1-2H2

543-20-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A18389)  Succinyl chloride, 96%   

  • 543-20-4

  • 50g

  • 312.0CNY

  • Detail
  • Alfa Aesar

  • (A18389)  Succinyl chloride, 96%   

  • 543-20-4

  • 250g

  • 1446.0CNY

  • Detail
  • Aldrich

  • (S6452)  Succinylchloride  95%

  • 543-20-4

  • S6452-25G

  • 814.32CNY

  • Detail
  • Aldrich

  • (S6452)  Succinylchloride  95%

  • 543-20-4

  • S6452-100G

  • 2,699.19CNY

  • Detail

543-20-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name SUCCINYL CHLORIDE

1.2 Other means of identification

Product number -
Other names Butanedioyl dichloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:543-20-4 SDS

543-20-4Synthetic route

succinic acid
110-15-6

succinic acid

succinoyl dichloride
543-20-4

succinoyl dichloride

Conditions
ConditionsYield
With thionyl chloride for 4h; Inert atmosphere; Schlenk technique; Reflux;99%
With phosgene; N,N-dimethyl-formamide In toluene at 55℃; Product distribution / selectivity;98.2%
With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 0 - 20℃; for 3h;95%
succinic acid anhydride
108-30-5

succinic acid anhydride

succinoyl dichloride
543-20-4

succinoyl dichloride

Conditions
ConditionsYield
With thionyl chloride at 80℃; for 4h;93%
With thionyl chloride; zinc(II) chloride at 120 - 145℃;
With thionyl chloride; copper(l) chloride; zinc(II) chloride at 120 - 145℃;
succinic acid anhydride
108-30-5

succinic acid anhydride

Dichloromethyl methyl ether
4885-02-3

Dichloromethyl methyl ether

(E)-3-Ureido-but-2-enoic acid ethyl ester
5435-44-9, 22243-66-9

(E)-3-Ureido-but-2-enoic acid ethyl ester

A

Methyl formate
107-31-3

Methyl formate

B

succinoyl dichloride
543-20-4

succinoyl dichloride

succinic acid anhydride
108-30-5

succinic acid anhydride

Dichloromethyl methyl ether
4885-02-3

Dichloromethyl methyl ether

succinoyl dichloride
543-20-4

succinoyl dichloride

Conditions
ConditionsYield
With zinc(II) chloride
succinic acid dihydrazide
4146-43-4

succinic acid dihydrazide

succinoyl dichloride
543-20-4

succinoyl dichloride

Conditions
ConditionsYield
With hydrogenchloride; nitromethane; chlorine
succinic acid anhydride
108-30-5

succinic acid anhydride

phosphorus pentachloride
10026-13-8, 874483-75-7

phosphorus pentachloride

succinoyl dichloride
543-20-4

succinoyl dichloride

Conditions
ConditionsYield
at 120 - 130℃;
trimer(ic) β-aldehydo-propionic acid

trimer(ic) β-aldehydo-propionic acid

succinoyl dichloride
543-20-4

succinoyl dichloride

Conditions
ConditionsYield
With phosphorus pentachloride
succinic acid
110-15-6

succinic acid

PCl5 (2 mol)

PCl5 (2 mol)

succinoyl dichloride
543-20-4

succinoyl dichloride

thionyl chloride
7719-09-7

thionyl chloride

succinic acid
110-15-6

succinic acid

ZnCl2

ZnCl2

CuCl

CuCl

succinoyl dichloride
543-20-4

succinoyl dichloride

Conditions
ConditionsYield
at 120 - 145℃;
Succinic semialdehyde
692-29-5

Succinic semialdehyde

phosphorus pentachloride
10026-13-8, 874483-75-7

phosphorus pentachloride

A

succinoyl dichloride
543-20-4

succinoyl dichloride

B

γ-chloro-butyrolactone

γ-chloro-butyrolactone

1,5-pentanedioic acid
110-94-1

1,5-pentanedioic acid

Adipic acid
124-04-9

Adipic acid

succinic acid
110-15-6

succinic acid

A

gloutaric dichloride
2873-74-7

gloutaric dichloride

B

succinoyl dichloride
543-20-4

succinoyl dichloride

C

Adipic acid dichloride
111-50-2

Adipic acid dichloride

Conditions
ConditionsYield
With thionyl chloride at 20℃;
thiophenol
108-98-5

thiophenol

succinoyl dichloride
543-20-4

succinoyl dichloride

S,S'-diphenyl dithiosuccinate
29549-28-8

S,S'-diphenyl dithiosuccinate

Conditions
ConditionsYield
With tetrabutyl-ammonium chloride; sodium hydroxide In dichloromethane; water at 0℃; for 0.0833333h;100%
With silica gel at 20℃; for 4h;72%
succinoyl dichloride
543-20-4

succinoyl dichloride

dimethyl amine
124-40-3

dimethyl amine

N,N,N',N'-tetramethylsuccinamide
7334-51-2

N,N,N',N'-tetramethylsuccinamide

Conditions
ConditionsYield
In water at 0℃; for 0.5h;100%
In diethyl ether at -78 - 20℃;91%
In dichloromethane; water at 0 - 20℃; for 20h; Inert atmosphere;81%
With diethyl ether
In water at 0℃; for 0.5h;
trimethylsilyl cyanide
7677-24-9

trimethylsilyl cyanide

succinoyl dichloride
543-20-4

succinoyl dichloride

Succinyl Dicyanide
63979-84-0

Succinyl Dicyanide

Conditions
ConditionsYield
With chloro-trimethyl-silane at 20℃; for 72h; Inert atmosphere;100%
for 168h; Ambient temperature;63%
thiophene
188290-36-0

thiophene

succinoyl dichloride
543-20-4

succinoyl dichloride

1,4-bis(thiophen-2-yl)butane-1,4-dione
13669-05-1

1,4-bis(thiophen-2-yl)butane-1,4-dione

Conditions
ConditionsYield
With ethylaluminum dichloride In dichloromethane at 0℃; for 2h; Inert atmosphere;99%
With aluminum (III) chloride In N,N-dimethyl-formamide at 20℃; Inert atmosphere;84%
With aluminum (III) chloride In dichloromethane at 20℃; for 20h; Friedel-Crafts Acylation;82%
methanol
67-56-1

methanol

ethylaluminum dichloride
563-43-9

ethylaluminum dichloride

succinoyl dichloride
543-20-4

succinoyl dichloride

methyl 4-oxohexanoate
2955-62-6

methyl 4-oxohexanoate

Conditions
ConditionsYield
In dichloromethane at -40℃; for 3.5h;99%
Stage #1: ethylaluminum dichloride; succinoyl dichloride In dichloromethane at -40℃; for 3.5h;
Stage #2: methanol In dichloromethane at -40℃;
99%
thymol
89-83-8

thymol

succinoyl dichloride
543-20-4

succinoyl dichloride

thymol succinate

thymol succinate

Conditions
ConditionsYield
With sodium hydroxide for 0.05h; microwave irradiation;99%
thymol
89-83-8

thymol

succinoyl dichloride
543-20-4

succinoyl dichloride

Amberlite IRA-400 (chloride form) resin

Amberlite IRA-400 (chloride form) resin

thymol succinate

thymol succinate

Conditions
ConditionsYield
Stage #1: thymol; Amberlite IRA-400 (chloride form) resin With sodium hydroxide
Stage #2: succinoyl dichloride In benzene
98%
1,6-diamino-1,6-dideoxy-3,4-O-isopropylidene-D-mannitol
501668-81-1

1,6-diamino-1,6-dideoxy-3,4-O-isopropylidene-D-mannitol

succinoyl dichloride
543-20-4

succinoyl dichloride

poly(1,6-dideoxy-3,4-di-O-isopropylidene-D-mannitolsuccinimide); monomer(s): 1,6-diamino-1,6-dideoxy-3,4-di-O-isopropylidene-D-mannitol; succinoyl dichloride

poly(1,6-dideoxy-3,4-di-O-isopropylidene-D-mannitolsuccinimide); monomer(s): 1,6-diamino-1,6-dideoxy-3,4-di-O-isopropylidene-D-mannitol; succinoyl dichloride

Conditions
ConditionsYield
With sodium carbonate In tetrachloromethane at 20℃; for 3h;98%
(Z)-2-(3,4-dimethoxy-phenyl)-3-(4-hydroxy-phenyl)-acrylonitrile
741737-80-4

(Z)-2-(3,4-dimethoxy-phenyl)-3-(4-hydroxy-phenyl)-acrylonitrile

succinoyl dichloride
543-20-4

succinoyl dichloride

bis-{4-[(Z)-2-cyano-2-(3,4-dimethoxy-phenyl)-vinyl]-phenyl} succinate

bis-{4-[(Z)-2-cyano-2-(3,4-dimethoxy-phenyl)-vinyl]-phenyl} succinate

Conditions
ConditionsYield
With pyridine98%
(μ-dithio)bis(tricarbonyliron)
14243-23-3

(μ-dithio)bis(tricarbonyliron)

succinoyl dichloride
543-20-4

succinoyl dichloride

para-methylphenylmagnesium bromide
4294-57-9

para-methylphenylmagnesium bromide

(CH3C6H4SFe2(CO)6SCO)2C2H4

(CH3C6H4SFe2(CO)6SCO)2C2H4

Conditions
ConditionsYield
In tetrahydrofuran p-TolMgBr in THF was added under N2 with stirring to a THF soln. of Fe2-complex at -78°C, ClCOCH2CH2COCl (1/2 molar equiv) was added to the resulting anion soln. at -78°C, mixt. was allowed to warm to room temp.; volatiles were removed, residue purified by column chromy.; elem. anal.;98%
benzyl (S)-Lactate
56777-24-3

benzyl (S)-Lactate

succinoyl dichloride
543-20-4

succinoyl dichloride

Succinic acid bis-((S)-1-benzyloxycarbonyl-ethyl) ester
314069-31-3

Succinic acid bis-((S)-1-benzyloxycarbonyl-ethyl) ester

Conditions
ConditionsYield
With pyridine In dichloromethane at 25℃; under 2585.74 Torr; for 16h;97%
With pyridine In dichloromethane at 0℃;
C58H68O2Si3
959397-89-8

C58H68O2Si3

succinoyl dichloride
543-20-4

succinoyl dichloride

(C58H67O2Si3)2COCOCH2CH2

(C58H67O2Si3)2COCOCH2CH2

Conditions
ConditionsYield
With dmap In dichloromethane at 20℃; for 0.216667h;97%
With dmap In dichloromethane at 20℃; for 0.133333h; Inert atmosphere;97%
succinoyl dichloride
543-20-4

succinoyl dichloride

12-(p-aminophenyl)-9,9-dimethyl-8,9,10,11-tetrahydrobenzacridin-11-one
159146-73-3

12-(p-aminophenyl)-9,9-dimethyl-8,9,10,11-tetrahydrobenzacridin-11-one

N,N'-bis-[4-(9,9-dimethyl-11-oxo-8,9,10,11-tetrahydro-benzo[a]acridin-12-yl)-phenyl]-succinamide

N,N'-bis-[4-(9,9-dimethyl-11-oxo-8,9,10,11-tetrahydro-benzo[a]acridin-12-yl)-phenyl]-succinamide

Conditions
ConditionsYield
In acetone at 5℃; for 0.25h;96%
succinoyl dichloride
543-20-4

succinoyl dichloride

aniline
62-53-3

aniline

Succinanilid
15510-09-5

Succinanilid

Conditions
ConditionsYield
In pyridine at 20℃; for 24h;95%
With benzene
2,5-dimethyl-2,5-dihydroperoxyhexane
3025-88-5

2,5-dimethyl-2,5-dihydroperoxyhexane

succinoyl dichloride
543-20-4

succinoyl dichloride

Phthaloyl dichloride
88-95-9

Phthaloyl dichloride

2-(4-{2-[4-(3-{4-[3-(4-Hydroperoxy-1,1,4-trimethyl-pentylperoxycarbonyl)-propionylperoxy]-1,1,4-trimethyl-pentylperoxycarbonyl}-propionylperoxy)-1,1,4-trimethyl-pentylperoxycarbonyl]-benzoylperoxy}-1,1,4-trimethyl-pentylperoxycarbonyl)-benzoic acid
78491-83-5

2-(4-{2-[4-(3-{4-[3-(4-Hydroperoxy-1,1,4-trimethyl-pentylperoxycarbonyl)-propionylperoxy]-1,1,4-trimethyl-pentylperoxycarbonyl}-propionylperoxy)-1,1,4-trimethyl-pentylperoxycarbonyl]-benzoylperoxy}-1,1,4-trimethyl-pentylperoxycarbonyl)-benzoic acid

Conditions
ConditionsYield
With pyridine In dichloromethane at 20℃; for 1.5h;95%
Conditions
ConditionsYield
With triethylamine In N,N-dimethyl-formamide for 3h; Ambient temperature;95%
7-hydroxy-4-methyl-chromen-2-one
90-33-5, 79566-13-5

7-hydroxy-4-methyl-chromen-2-one

succinoyl dichloride
543-20-4

succinoyl dichloride

succinic acid bis-(4-methyl-2-oxo-2H-chromen-7-yl) ester

succinic acid bis-(4-methyl-2-oxo-2H-chromen-7-yl) ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 2h;95%
succinoyl dichloride
543-20-4

succinoyl dichloride

Nε-lauroyl-L-lysine ethyl ester
292140-08-0

Nε-lauroyl-L-lysine ethyl ester

Nα,Nα'-succinyl-bis(Nε-lauroyl-L-lysine ethyl ester)

Nα,Nα'-succinyl-bis(Nε-lauroyl-L-lysine ethyl ester)

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 20℃; for 24h;95%
succinoyl dichloride
543-20-4

succinoyl dichloride

acetyl chloride
75-36-5

acetyl chloride

diphenyl succinate
621-14-7

diphenyl succinate

Conditions
ConditionsYield
With tetrabutyl-ammonium chloride; sodium hydroxide In dichloromethane; water at 0℃; for 0.0833333h;95%
succinoyl dichloride
543-20-4

succinoyl dichloride

para-methylbenzonitrile
104-85-8

para-methylbenzonitrile

2,2'-(1,2-Ethandiyl)bis<4,6-bis(p-tolyl)-1,3,5-oxadiazinium>-dihexachloroantimonat(V)

2,2'-(1,2-Ethandiyl)bis<4,6-bis(p-tolyl)-1,3,5-oxadiazinium>-dihexachloroantimonat(V)

Conditions
ConditionsYield
With antimonypentachloride In tetrachloromethane for 5h; Heating;94%
With antimonypentachloride In dichloromethane 1) -40 to 25 deg C, 2) 25 deg C, 3 h;75%
succinoyl dichloride
543-20-4

succinoyl dichloride

7-(p-Aminophenyl)-10,10-dimethyl-8,9,10,11-tetrahydrobenz[c]acridin-8-one
117358-75-5

7-(p-Aminophenyl)-10,10-dimethyl-8,9,10,11-tetrahydrobenz[c]acridin-8-one

N,N'-bis-[4-(10,10-dimethyl-8-oxo-8,9,10,11-tetrahydro-benzo[c]acridin-7-yl)-phenyl]-succinamide

N,N'-bis-[4-(10,10-dimethyl-8-oxo-8,9,10,11-tetrahydro-benzo[c]acridin-7-yl)-phenyl]-succinamide

Conditions
ConditionsYield
In acetone at 5℃; for 0.25h;94%
succinoyl dichloride
543-20-4

succinoyl dichloride

2-Mercaptobenzothiazole
149-30-4

2-Mercaptobenzothiazole

dithiosuccinic acid di-S-benzothiazol-2-yl ester

dithiosuccinic acid di-S-benzothiazol-2-yl ester

Conditions
ConditionsYield
With sodium hydroxide; Amberlite IRA-400 chloride form In water; acetone94%
Stage #1: 2-Mercaptobenzothiazole With aluminum oxide; silica gel; sodium carbonate; fly ash microwave oven;
Stage #2: succinoyl dichloride microwave irradiation;
N-hydroxyphthalimide
524-38-9

N-hydroxyphthalimide

succinoyl dichloride
543-20-4

succinoyl dichloride

O,O′-succinyloyl-bis-N,N′-phthalimide ester

O,O′-succinyloyl-bis-N,N′-phthalimide ester

Conditions
ConditionsYield
Stage #1: N-hydroxyphthalimide With sodium hydroxide; Amberlite IRA-400 chloride form
Stage #2: succinoyl dichloride In tetrahydrofuran at 20℃;
94%
With pyridine at 20℃; for 24h;60%
succinoyl dichloride
543-20-4

succinoyl dichloride

m,p-dichloroaniline
95-76-1

m,p-dichloroaniline

N,N'-bis(3,4-dichlorophenyl)butanediamide

N,N'-bis(3,4-dichlorophenyl)butanediamide

Conditions
ConditionsYield
In pyridine at 20℃; for 24h;93%
(1R,2R,3S,5S)-3-(3,4-dichlorophenyl)-2-hydroxymethyl-8-thiabicyclo[3.2.1]octane
1020108-12-6

(1R,2R,3S,5S)-3-(3,4-dichlorophenyl)-2-hydroxymethyl-8-thiabicyclo[3.2.1]octane

succinoyl dichloride
543-20-4

succinoyl dichloride

(3β-(3,4-dichlorophenyl)-8-thiabicyclo[3.2.1]octan-2β-yl)methyl,(3β-(3,4-dichlorophenyl)-8-thiabicyclo[3.2.1]octan-2β-yl)methyl succinate
1020108-07-9

(3β-(3,4-dichlorophenyl)-8-thiabicyclo[3.2.1]octan-2β-yl)methyl,(3β-(3,4-dichlorophenyl)-8-thiabicyclo[3.2.1]octan-2β-yl)methyl succinate

Conditions
ConditionsYield
With dmap In dichloromethane at 0 - 20℃;93%
octaethylene glycol monomethyl ether
25990-96-9

octaethylene glycol monomethyl ether

succinoyl dichloride
543-20-4

succinoyl dichloride

C21H39ClO11

C21H39ClO11

Conditions
ConditionsYield
Stage #1: octaethylene glycol monomethyl ether With sodium hydride In tetrahydrofuran at -20℃; for 0.5h;
Stage #2: succinoyl dichloride In tetrahydrofuran at -20 - 20℃;
93%
ethylbenzene
100-41-4

ethylbenzene

succinoyl dichloride
543-20-4

succinoyl dichloride

1,4-bis(4-ethylphenyl)butane-1,4-dione

1,4-bis(4-ethylphenyl)butane-1,4-dione

Conditions
ConditionsYield
With aluminum (III) chloride In benzene at 0 - 20℃; Friedel-Crafts acylation; Inert atmosphere;93%
succinoyl dichloride
543-20-4

succinoyl dichloride

toluene
108-88-3

toluene

1,4-bis(4-tolyl)butane-1,4-dione
13145-56-7

1,4-bis(4-tolyl)butane-1,4-dione

Conditions
ConditionsYield
With aluminum (III) chloride In benzene at 0 - 20℃; Friedel-Crafts acylation; Inert atmosphere;92%
Stage #1: succinoyl dichloride; toluene With aluminum (III) chloride In dichloromethane at 0℃; for 0.5h;
Stage #2: With hydrogenchloride
73%
With aluminium trichloride
With aluminium trichloride

543-20-4Relevant articles and documents

Modulation of charge transport through single-molecule bilactam junctions by tuning hydrogen bonds

Chen, Yaorong,Wang, Hua-Chun,Tang, Yongxiang,Zhou, Yu,Huang, Longfeng,Cao, Jian,Tang, Chun,Zhang, Manxi,Shi, Jia,Liu, Junyang,Ren, Xiancheng,Xu, Yun-Xiang,Hong, Wenjing

, p. 1935 - 1938 (2021)

Bilactam derivatives with different side groups were synthesized and the twisting angle tuning effect induced by the intramolecular hydrogen bond on the charge transport through their single-molecule junctions was investigated. Molecules with strong intramolecular hydrogen bonds exhibited twice higher conductance because of the reduced dihedral twisting, which was reversible with the addition of hydrogen bond destroying solvent. Our findings reveal that the presence of intramolecular hydrogen bonds promotes the planarization of the molecular structure without additional transmission channels, offering a new strategy for controlling molecular switchesviatuning the molecular twisting.

Dimeric 3,5-bis(benzylidene)-4-piperidones: A novel cluster of tumour-selective cytotoxins possessing multidrug-resistant properties

Das, Swagatika,Das, Umashankar,Sakagami, Hiroshi,Umemura, Naoki,Iwamoto, Shoko,Matsuta, Tomohiko,Kawase, Masami,Molnár, Joseph,Serly, Julianna,Gorecki, Dennis K.J.,Dimmock, Jonathan R.

, p. 193 - 199 (2012)

A series of bis[3,5-bis(benzylidene)-4-oxo-1-piperidinyl]amides 1 display potent cytotoxic properties towards a wide range of tumours. A number of the CC50 and IC50 values are in the range of 10-8 M. Specifically, these compounds have the following important properties. First, greater toxicity was demonstrated towards certain tumours than various non-malignant cells. Second, various compounds in series 1 are toxic to a number of human colon cancer and leukaemic cells. Third, these compounds reverse P-gp mediated multidrug resistance. Various prototypic molecules such as 1a,b and 1i were identified as lead molecules for further studies. A representative lead molecule 1b induces apoptosis via internucleosomal DNA fragmentation and PARP cleavage in HSC-2 and HL-60 cells while flow cytometry revealed that this compound blocked the G2/M and S-phases in the cell cycle of human colon cancer HCT-116 cells.

Ruthenium-catalyzed cascade metathetical cyclopolymerization of bisnorbornenes with flexible linkers

Chen, Chung-Hsuan,Chen, Chun-Hsien,Zhu, Lei,Lin, Nai-Ti,Xie, Zhen-Yu,Lee, Shern-Long,Huang, Shou-Ling,Yang, Jian-He,Lee, Yu-Der,Luh, Tien-Yau

, p. 656 - 663 (2013)

Treatments of bisnorbornenes tethered by a flexible linker (triethylene glycol, tetramethylene moiety, or crown ether) with the first generation of Grubbs catalyst give the corresponding single-stranded polybisnorbornenes via cascade metathetical cyclopolymerization (CMCP). The structures of these polymers were proved by spectroscopic means, MALDI-TOF mass spectrometry, gel permeation chromatography, and dynamic light scatterings as well as by chemical degradation via hydrolysis followed by esterification. The presence of N-aryl pendants to connect the norbornene moiety and the flexible linker is crucial for the success of such CMCP process. Presumably, intramolecular π-π interactions between the pending aryl groups may take place to direct the ring closure process. Substrates without such N-aryl pendants give a mixture of single- and double-stranded polynorbornenes in addition to cross-linking polymers.

Citrate plasticizer and preparation method thereof

-

Paragraph 0059; 0062, (2021/05/29)

The invention discloses a citrate plasticizer and a preparation method thereof. The preparation method comprises the following steps: firstly, carrying out reaction on citric acid and alcohol to prepare citric acid triester; acylating dianhydride to prepare carboxyl-containing triester citrate; carrying out acylating chlorination on the carboxyl-containing triester citrate, and then carrying out esterification reaction on the carboxyl-containing triester citrate and tri(2-hydroxyethyl) isocyanurate to prepare triester citrate containing isocyanurate; and finally, esterifying with fatty acyl chloride to obtain the modified citrate plasticizer. The preparation method is simple to operate, wide in raw material source and mild in reaction condition, and meets industrial production. The prepared triester citrate containing isocyanurate has a good plasticizing effect and excellent thermal stability, low-temperature flexibility, solvent extraction resistance, migration resistance and flame retardance, and can be widely applied to plastic rubber plasticizers.

Refining method of succinylcholine chloride

-

Paragraph 0040-0041, (2020/02/14)

The invention discloses a refining method of succinylcholine chloride. A crude product of succinylcholine chloride is added into a polar aprotic solvent and recrystallized to obtain a refined productof succinylcholine chloride, and related substances of the product meet USP pharmacopoeia standards. The invention provides a refining method of succinylcholine chloride with simple process, convenient operation, low production cost, high product purity, stable process and suitability for industrial production, and also provides a raw material or bulk drug of high-purity succinylcholine chloride.

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