ChemicalBook > CAS DataBase List > N-Iodosuccinimide

N-Iodosuccinimide

Product Name
N-Iodosuccinimide
CAS No.
516-12-1
Chemical Name
N-Iodosuccinimide
Synonyms
NIS;1-iodopyrrolidine-2,5-dione;Iodosuccinimide;N-IodosucciniMide (NIS);1-IODO-2,5-PYRROLIDINEDIONE;N-iododiimide;succiniodimide;N-IODOSUCCINIMIDE;n-iodo-succinimid;N-lodosuccinimide
CBNumber
CB0342078
Molecular Formula
C4H4INO2
Formula Weight
224.98
MOL File
516-12-1.mol
More
Less

N-Iodosuccinimide Property

Melting point:
202-206 °C(lit.)
Boiling point:
249.6±23.0 °C(Predicted)
Density 
2,245 g/cm3
storage temp. 
2-8°C
solubility 
Soluble in dioxane, tetrahydrfuran and acetonitrile. Insoluble in ether and carbon tetrachloride.
pka
-2.57±0.20(Predicted)
form 
Crystalline Powder
color 
White-yellow to brown
Water Solubility 
decomposes
Sensitive 
Moisture Sensitive
Merck 
14,5045
BRN 
113917
Stability:
Moisture Sensitive
InChIKey
LQZMLBORDGWNPD-UHFFFAOYSA-N
CAS DataBase Reference
516-12-1(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
Xn,Xi
Risk Statements 
22-36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
RTECS 
WN2817000
8-9
Hazard Note 
Harmful/Keep Cold/Moisture Sensitive
TSCA 
No
HazardClass 
IRRITANT
HS Code 
29251995
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H317May cause an allergic skin reaction

H319Causes serious eye irritation

H341Suspected of causing genetic defects

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P201Obtain special instructions before use.

P273Avoid release to the environment.

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

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P308+P313IF exposed or concerned: Get medical advice/attention.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
220051
Product name
N-Iodosuccinimide
Purity
95%
Packaging
5g
Price
$58.9
Updated
2024/03/01
Sigma-Aldrich
Product number
220051
Product name
N-Iodosuccinimide
Purity
95%
Packaging
25g
Price
$126
Updated
2024/03/01
TCI Chemical
Product number
I0074
Product name
N-Iodosuccinimide
Purity
>98.0%(T)
Packaging
5g
Price
$47
Updated
2024/03/01
TCI Chemical
Product number
I0074
Product name
N-Iodosuccinimide
Purity
>98.0%(T)
Packaging
25g
Price
$134
Updated
2024/03/01
Alfa Aesar
Product number
A14320
Product name
N-Iodosuccinimide, 97%
Packaging
5g
Price
$53.1
Updated
2024/03/01
More
Less

N-Iodosuccinimide Chemical Properties,Usage,Production

Chemical Properties

white-yellow to brown crystalline powder

Uses

Iodination of ketones and aldehydes.
Highly substituted iodobenzenes prepared via an efficient 2-step process from 1,6-diynes.
Used with TFA to chemoselectively hydrolyze thioglycosides to 1-hydroxyglycosides.
Synthesis of vinyl sulfones from olefins and benzenesulfinic acid.

Uses

N-Iodosuccinimide is used in the preparation of vinyl sulfones from olefins and benzenesulfinic acid. It acts as a source for I+ and involved in Hunsdiecker reactions for the conversion of cinnamic acids, and propiolic acids to the corresponding alfa-halostyrenes and 1-halo-1-alkynes respectively. It is also used to hydrolyze thioglycosides to 1-hydroxyglycosides with triluoroacetic acid. It is involved in the preparation of iodobenzene from 1,6-diynes. Further, it acts as an iodinating agent in chemical synthesis.

Uses

N-Iodosuccinimide is a iodo substituted succinimide that is used as an iodinating agent in chemical synthesis.

Preparation

To a solution of 39.2g of succinimide in 1200ml of boiling water was added 51.0g of freshly precipitated silver oxide, the mixture was filtered and the silver salt was allowed to crystallize. Filtration and washing with cold water furnished 45.0g of the silver salt of succinimide suitable for the iodination step.
The finely powdered salt (49.5g) was added in portions with stirring to a solution of 50.8g of iodine in 300ml of acetone, the temperature being maintained at 5-10°C. After decolorization (30 min.), the silver iodide was filtered, the solvent was removed under reduced pressure at room temperature and the residue was washed with ether, yielding 43g of N-iodosuccinimide with mp 189-191°C. An analytical sample (85% recovery) was obtained by dissolving in the minimum quantity of hot dioxane and precipitating with carbon tetrachloride; colorless needles, mp 200-201°C.
Ref: JACS 75, 3493 (1953)

Definition

ChEBI: N-iodosuccinimide is a five-membered cyclic dicarboximide compound having an iodo substituent on the nitrogen atom. It is a dicarboximide and a pyrrolidinone. It derives from a succinimide.

Reactions

N-Iodosuccinimide (NIS) is an iodinating agent that is used for various electrophilic iodinations and as source for iodine in radical reactions.
N-Iodosuccinimide is the least reactive of the N-haloamides in aromatic substitution. N-Iodosuccinimide does not act as an iodinating agent in pure dimethyl sulfoxide or N-ethylacetamide. On the other hand, butyl disulfide and a number of other sulfur-containing compounds are effective catalysts at low concentration for the iodination of guanosine derivatives using N-iodosuccinimide. This catalytic effect is observed when dimethyl sulfoxide is used as the solvent,but not when N-ethylacetamide is used.
https://www.organic-chemistry.org/chemicals/oxidations/n-iodosuccinimide-nis.shtm

Synthesis Reference(s)

Journal of the American Chemical Society, 75, p. 3493, 1953 DOI: 10.1021/ja01110a055
Organic Syntheses, Coll. Vol. 5, p. 663, 1973
Tetrahedron Letters, 25, p. 233, 1984 DOI: 10.1016/S0040-4039(00)99848-4

Purification Methods

Crystallise it from dioxane/CCl4. It iodinates arenes in triflic acid. [Olah et al J Org Chem 58 3194 1993, Beilstein 21/9 V 544.]

N-Iodosuccinimide Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

N-Iodosuccinimide Suppliers

Nanjing Hengweisheng Pharmaceutical Technology Co., Ltd
Tel
19941530336
Email
3991044086@qq.com
Country
China
ProdList
682
Advantage
58
Jinan Dexinjia Bio&Tech Co., Ltd
Tel
0531-82375886 13001715031
Fax
0531-82375893
Email
3517280075@qq.com
Country
China
ProdList
1312
Advantage
58
Shanghai Witofly Chemical Co. ,Ltd.
Tel
021-5063062 15300832537
Email
sales@witofly.com
Country
China
ProdList
1603
Advantage
55
Beijing Xinze Pharmaceutical Technology Co., Ltd.
Tel
010-61393740 13121768631
Email
weihong_1979@163.com
Country
China
ProdList
49
Advantage
58
Wuhu Nuowei Chemical Technology Co., Ltd
Tel
0553-2911116 18055326116
Email
sales@nuowei-chem.com
Country
China
ProdList
309
Advantage
58
Shanghai Qiao Chemical Science Co., Ltd
Tel
021-58892003
Email
info@qiaochem.com
Country
China
ProdList
5902
Advantage
65
Chongqing Yuzhiquan Biological Technology Co., Ltd.
Tel
18306022109
Fax
QQ:2966918840
Email
3236923470@qq.com
Country
China
ProdList
296
Advantage
58
NINGBO JL NEW MATERIAL CO.,LTD
Tel
0574-88552218 18969899212
Email
sales@jlbio-tech.cn
Country
China
ProdList
715
Advantage
58
Shanghai NAIFU Biotechnology Co., Ltd
Tel
18939876937 18939876937
Email
sales@naifuchem.com
Country
China
ProdList
49
Advantage
58
Hbzzksw
Tel
13284332550
Email
2277858663@qq.com
Country
China
ProdList
32
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
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15839
Advantage
69
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
Beijing HwrkChemical Technology Co., Ltd
Tel
010-89508211 18501085097
Fax
010-89508210
Email
sales.bj@hwrkchemical.com
Country
China
ProdList
8418
Advantage
55
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44689
Advantage
61
Shijiazhuang Sdyano Fine Chemical Co., Ltd.
Tel
0311-89250318 031166536426
Fax
4000311741
Email
master@sjzsdyn.com
Country
China
ProdList
2963
Advantage
65
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Fax
86-027-87531808
Email
sales@chemwish.com
Country
China
ProdList
35896
Advantage
56
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Fax
0086-571-85864795
Email
sales@capotchem.com
Country
China
ProdList
18207
Advantage
66
Beijing Ouhe Technology Co., Ltd
Tel
010-82967028 13552068683
Fax
+86-10-82967029
Email
2355560935@qq.com
Country
China
ProdList
12390
Advantage
60
JinYan Chemicals(ShangHai) Co.,Ltd.
Tel
13817811078
Fax
86-021-50426522,50426273
Email
sales@jingyan-chemical.com
Country
China
ProdList
9976
Advantage
60
Shanghai Sinch Parmaceuticals Tech. Co. Ltd.
Tel
+86-21-54098501
Fax
+86-21-54096319
Email
sales@sinch.com.cn
Country
China
ProdList
11598
Advantage
64
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Fax
0573-85285100
Email
isenchem@163.com
Country
China
ProdList
9413
Advantage
66
Accela ChemBio Co.,Ltd.
Tel
021-50795510 4000665055
Fax
021-50795055
Email
sales@accelachem.com
Country
China
ProdList
11655
Advantage
64
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
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12984
Advantage
57
Sichuan Kulinan Technology Co., Ltd
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11707
Advantage
57
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14435
Advantage
57
Shanghai Sunway Pharmaceutical Technology Co., Ltd
Tel
021-51613915-820 13611835272
Fax
021 51613951
Email
mmwang@sunwaypharm.cn
Country
China
ProdList
9734
Advantage
57
Hunan Hui Bai Shi Biotechnology Co., Ltd.
Tel
0731-85526065 13308475853
Email
ivy@hnhbsj.com
Country
China
ProdList
4552
Advantage
62
Nanjing Vital Chemical Co., Ltd.
Tel
Please Send Email 18652950785
Fax
025-87193546
Email
chemweiao@163.com
Country
China
ProdList
4378
Advantage
65
Maya High Purity Chemicals
Tel
+86 (573) 82222445 (0)18006601000 452520369
Fax
+86 (573) 82222643
Email
sales@maya-r.com
Country
China
ProdList
11707
Advantage
57
Hangzhou Yuhao Chemical Technology Co., Ltd
Tel
0571-82693216
Fax
+86-571-82880190
Email
info@yuhaochemical.com
Country
China
ProdList
9387
Advantage
52
ZhengZhou HuaWen Chemical Co.Ltd
Tel
0370-2785118 17550508557
Fax
QQ:3470079902
Email
675141927@qq.com
Country
China
ProdList
3203
Advantage
55
Shanghai Sphchem Co., Ltd.
Tel
21-21-56491756 13512199871
Fax
021-5649-1756
Email
sales@panhongchem.com
Country
China
ProdList
4000
Advantage
55
Beijing Taiya Jie Technology Development Co., Ltd.
Tel
021-33690831-8001 13552411790
Fax
021-33690831
Email
postmaster@tyjchem.cn
Country
China
ProdList
1541
Advantage
55
Spectrum Chemical Manufacturing Corp.
Tel
021-021-021-67601398-809-809-809 15221380277
Fax
021-57711696
Email
marketing_china@spectrumchemical.com
Country
China
ProdList
9658
Advantage
60
ShangHai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847 13636370518
Fax
021-55068248
Email
shyysw007@163.com
Country
China
ProdList
4940
Advantage
60
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9718
Advantage
55
Shanghai civi chemical technology co.,Ltd
Tel
86-21-34053660
Fax
86-21-34053661
Email
sale@labgogo.com
Country
China
ProdList
9865
Advantage
52
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17770
Advantage
75
Beijing innoChem Science & Technology Co.,Ltd.
Tel
400-810-7969 010-59572699
Fax
010-59572688
Email
ningzi.li@inno-chem.com.cn
Country
China
ProdList
6134
Advantage
55
Shanghai Topbiochem Technology Co., Ltd
Tel
021-58170097
Email
info@topbiochem.com
Country
China
ProdList
9459
Advantage
58
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611
Fax
+86 21 50676805
Country
China
ProdList
9891
Advantage
58
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
Tel
025-66099280 17798518460
Fax
(1)02557626880
Email
cfzhang@aikonchem.com
Country
China
ProdList
19915
Advantage
55
SuZhou ShiYa Biopharmaceuticals, Inc.
Tel
86(512)5235 8471 17715136450
Fax
86(512)5235 6881
Email
sales@shiyabiopharm.com
Country
China
ProdList
4169
Advantage
58
More
Less

View Lastest Price from N-Iodosuccinimide manufacturers

Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
N-Iodosuccinimide 516-12-1
Price
US $10.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20ton
Release date
2024-05-06
HebeiShuoshengImportandExportco.,Ltd
Product
N-Iodosuccinimide 516-12-1
Price
US $6.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
2000KG/Month
Release date
2024-08-05
Hebei Longbang Technology Co., Ltd
Product
N-Iodosuccinimide 516-12-1
Price
US $6.00/kg
Min. Order
1kg
Purity
More than 99%
Supply Ability
2000KG/Month
Release date
2024-05-27

516-12-1, N-IodosuccinimideRelated Search:


  • 1-iodo-5-pyrrolidinedione
  • 1-IODO-2,5-PYRROLIDINEDIONE
  • NIS
  • N-IODOSUCCINIMIDE
  • N-Iodosuccinimide, 98+%
  • N-Iodosuccinimide ,99%
  • N-Iodosuccinimide , (1-Iodo-2,5-pyrrolidinedione)
  • 1-Iodopyrrolidine-2,5-dione, 2,5-Dioxo-1-iodopyrrolidine
  • N-IodosucciniMide (NIS)
  • N-IodosucciniMide, 98% 100GR
  • N-IodosucciniMide, 98% 10GR
  • N-iodobutanimide/NIS
  • N-IodosucciniMide / N-IodobutaniMide
  • N-iodoDing twoiMide
  • N - butyl diiMide iodine generation
  • <i>N</i>-Iodosuccinimide
  • 1-iodopyrrolidine-2,5-dione
  • Iodosuccinimide
  • 2,5-Pyrrolidinedione, 1-iodo-
  • N-Iodosuccinimide, 97+%
  • n-iodo-succinimid
  • Succinimide,N-iodo-
  • succiniodimide
  • N-Iodosuccinimide≥ 99.9% (Iodometry)
  • N-Iodosuccinimide, 97%, for synthesis
  • N-Iodosuccinimide&gt
  • N-IODOSUCCINIMIDE FOR SYNTHESIS
  • N-succinimide (NIS)
  • N-iododiimide
  • N-iodosuccinimideb
  • Big Discount Purity 99% N-Iodosuccinimide CAS 516-12-1 with Best Quality
  • Intermediate Material N-Iodosuccinimide (NIS) CAS?516-12-1
  • N-Iodosuccinimide 5GM
  • N-Iodosuccinimide extrapure, 99%
  • IODOSUCCINIMIDE For Synthesis
  • N-lodosuccinimide
  • Ripretinib Impurity 39
  • N-Iodosuccinimide (1-Iodopyrrolidine-2,5-Dione)
  • 516-12-1
  • 208-221-6
  • 512-12-1
  • C4H4INO2
  • C4H4O2NI
  • Reagents for Oligosaccharide Synthesis
  • Iodination
  • N-Substituted Succinimides
  • N-Substituted Maleimides, Succinimides & Phthalimides
  • Halogenation
  • C-X Bond Formation (Halogen)
  • Synthetic Reagents
  • C-X Bond Formation (Halogen)
  • Synthetic Reagents
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • API intermediates
  • Biochemistry
  • Halogenation
  • Iodination
  • N-Substituted Maleimides, Succinimides & Phthalimides