ChemicalBook > CAS DataBase List > Imidazolidine

Imidazolidine

Product Name
Imidazolidine
CAS No.
504-74-5
Chemical Name
Imidazolidine
Synonyms
imidazoline;mizuolin;Oil soluble imidazoline;Imidazolidine;1,3-Diazacyclopentane;Imidazolidine ISO 9001:2015 REACH;Imidazolidine (6CI, 8CI, 9CI, ACI)
CBNumber
CB71133311
Molecular Formula
C3H8N2
Formula Weight
72.11
MOL File
504-74-5.mol
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Imidazolidine Property

Melting point:
68.2-68.8 °C
Boiling point:
92.8±8.0 °C(Predicted)
Density 
0.892±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
10.33±0.20(Predicted)
EPA Substance Registry System
Imidazolidine (504-74-5)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Ambeed
Product number
A318836
Product name
Imidazolidine
Purity
90%inH2O
Packaging
5g
Price
$6
Updated
2021/12/16
Ambeed
Product number
A318836
Product name
Imidazolidine
Purity
90%inH2O
Packaging
25g
Price
$14
Updated
2021/12/16
Ambeed
Product number
A318836
Product name
Imidazolidine
Purity
90%inH2O
Packaging
100g
Price
$31
Updated
2021/12/16
Ambeed
Product number
A318836
Product name
Imidazolidine
Purity
90%inH2O
Packaging
500g
Price
$114
Updated
2021/12/16
Labseeker
Product number
SC-97431
Product name
Imidazolidine
Purity
98
Packaging
5g
Price
$283
Updated
2021/12/16
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Imidazolidine Chemical Properties,Usage,Production

Uses

The imidazolines, was discovered at American Cyanamid in the early 1980s. Extensive research has led to the development of four commercial compounds: imazapyr, imazamethabenzmethyl, imazethapyr, and imazaquin. Like the sulfonylureas, the imidazolines are extremely active at low rates.

Definition

ChEBI: Imidazolidine is a saturated organic heteromonocyclic parent, a member of imidazolidines and an azacycloalkane.

Synthesis

Imidazolidine is produced by a cyclocondensation reaction between ethylenediamine and an aldehyde. The yield is 70 %. The reaction conditions are that one of the amino groups of ethylenediamine is present using the secondary amine form.

Synthesis of Imidazolidine derivatives including:
(1) Synthesis of 1,3-dibenzyl-2-arylimidazolidine
It is divided into three steps: the first step is the condensation of ethylenediamine with aldehyde in dry benzene to obtain N,N′-dibenzylidene-1,2-diamine, and the second step is the reduction of N,N′-dibenzylidene ethylenediamine to N,N′-dibenzylidene ethylenediamine in ethanol with sodium borohydride. The substituted diamine was condensed with an aryl aldehyde in the final step to give 1,3-dibenzyl-2-arylimidazolidine.

(2)Synthesis of 2-iminoimidazolidine
Method: Ethylenediamine reacts with cyanobromide to form 2-iminoimidazolidine by substitution-cyclisation.

(3) Synthesis of Imidazolidin-2-one
Methods: Imidazolidin-2-one was prepared by heating ethylenediamine and urea with 75% yield.

Structure and conformation

Dihydroimidazole is a five-membered, nonplanar, and nonaromatic heterocycle, derived by the partial reduction of one of the two double bonds of the imidazole ring. The dihydroimidazoles are also referred to as imidazolines and there are three possible regioisomeric forms: 4,5-dihydroimidazole (2-imidazoline), 2,5-dihydroimidazole (3-imidazoline), and 2,3- dihydroimidazole (4-imidazoline). The 2- and 3-imidazolines contain an imine center, while 4-imidazoline contains an alkene substructure. Among these three isomeric forms, the chemistry of 2-imidazoline is more developed than 3- and 4-imidazolines.

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Imidazolidine Suppliers

Hubei Shiteng Chemical Technology Co. LTD
Tel
187-72749323 18971850150
Email
1273131441@qq.com
Country
China
ProdList
4989
Advantage
58
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
chenyj@titansci.com
Country
China
ProdList
14103
Advantage
59
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42958
Advantage
64
SpringPharma Tech Co.,Ltd
Tel
+86-25-68710855, +86-25-68710897
Fax
025-68710856
Email
sales@springpharma.net
Country
China
ProdList
1261
Advantage
62
Hangzhou Yuhao Chemical Technology Co., Ltd
Tel
0571-82693216
Fax
+86-571-82880190
Email
info@yuhaochemical.com
Country
China
ProdList
9387
Advantage
52
Hangzhou Sage Chemical Co., Ltd.
Tel
+86057186818502 13588463833
Fax
Pls mail us for more information!
Email
info@sagechem.com
Country
China
ProdList
10266
Advantage
58
Nanjing Sunlida Biological Technology Co., Ltd.
Tel
025-57798810
Fax
025-57019371
Email
sales@sunlidabio.com
Country
China
ProdList
3239
Advantage
55
Quzhou Juhua Friendship Co., Ltd
Tel
0570-3066667
Fax
0570-3063388
Country
China
ProdList
3930
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58
Shanghai JONLN Reagent Co., Ltd.
Tel
400-0066400 13621662912
Fax
021-55660885
Email
422131432@qq.com
Country
China
ProdList
9978
Advantage
55
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
41462
Advantage
60
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View Lastest Price from Imidazolidine manufacturers

Hebei Andu Technology Com.,Ltd
Product
Imidazolidine 504-74-5
Price
US $3.60/kg
Min. Order
1kg
Purity
≥99%
Supply Ability
3000tons/month
Release date
2024-07-25
Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
Imidazolidine 504-74-5
Price
US $70.00/kg
Min. Order
1kg
Purity
99
Supply Ability
5000
Release date
2024-05-22
HebeiShuoshengImportandExportco.,Ltd
Product
Imidazolidine 504-74-5
Price
US $6.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
2000KG/Month
Release date
2024-08-08