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3,4-Dinitrochlorobenzene

CAS No.
610-40-2
Chemical Name:
3,4-Dinitrochlorobenzene
Synonyms
3,4-DINITROCHLOROBENZENE;Bendamustine Impurity 54;4-Chloro-1,2-dinitrobenzen;3,4-Dinitrochlorobenzene>1-CHLORO-3,4-DINITROBENZENE;4-CHLORO-1,2-DINITROBENZENE;1,2-Dinitro-4-chlorobenzene;1,2-Dinitro-5-chlorobenzene;Benzene, 4-chloro-1,2-dinitro-;1-Chloro-3,4-dinitrobenzene, 92%+
CBNumber:
CB9691894
Molecular Formula:
C6H3ClN2O4
Molecular Weight:
202.55
MDL Number:
MFCD00007212
MOL File:
610-40-2.mol
MSDS File:
SDS
Last updated:2023-04-23 13:52:06

3,4-Dinitrochlorobenzene Properties

Melting point 40-41 °C
Boiling point 16 °C (4 mmHg)
Density 1.687 g/mL at 25 °C(lit.)
refractive index n20/D 1.587(lit.)
Flash point >230 °F
storage temp. 0-10°C
form Oily Liquid
color Yellow-brown
Water Solubility insoluble
BRN 521564
CAS DataBase Reference 610-40-2(CAS DataBase Reference)
FDA UNII Z29B1F274E
NIST Chemistry Reference Benzene, 4-chloro-1,2-dinitro-(610-40-2)
EPA Substance Registry System Benzene, 4-chloro-1,2-dinitro- (610-40-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS06,GHS07,GHS08,GHS09
Signal word  Danger
Hazard statements  H301+H311+H331-H317-H371-H373-H410-H300-H310-H330-H400
Precautionary statements  P260-P264-P270-P271-P272-P273-P280-P301+P310+P330-P302+P352+P312+P361+P364-P304+P340+P311-P308+P311-P391-P403+P233-P405-P501-P301+P310a-P304+P340-P320-P330-P501a
Hazard Codes  T,N
Risk Statements  23/24/25-33-50/53
Safety Statements  28-36/37-45-60-61-28A
RIDADR  UN 3441 6.1/PG 2
WGK Germany  3
TSCA  Yes
HazardClass  6.1
PackingGroup  II
HS Code  2904990090
NFPA 704
1
4 0

3,4-Dinitrochlorobenzene price More Price(14)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical D1900 3,4-Dinitrochlorobenzene >90.0%(GC) 610-40-2 25g $104 2024-03-01 Buy
Alfa Aesar B22773 1-Chloro-3,4-dinitrobenzene, tech. 90% 610-40-2 100g $57.65 2024-03-01 Buy
Alfa Aesar B22773 1-Chloro-3,4-dinitrobenzene, tech. 90% 610-40-2 250g $113.65 2024-03-01 Buy
TRC D482120 3,4-Dinitrochlorobenzene 610-40-2 50g $140 2021-12-16 Buy
TRC D482120 3,4-Dinitrochlorobenzene 610-40-2 10g $50 2021-12-16 Buy
Product number Packaging Price Buy
D1900 25g $104 Buy
B22773 100g $57.65 Buy
B22773 250g $113.65 Buy
D482120 50g $140 Buy
D482120 10g $50 Buy

3,4-Dinitrochlorobenzene Chemical Properties,Uses,Production

Description

Securinine is derived from the leaf of Securinega suffruticosa Rehd., which was first separated by V.I.?Murav’eva in 1956 . Securinega suffruticosa Rehd., a kind of subshrub plant, is widely distributed in temperate and subtropical regions . It has strong adaptability and can be planted in most parts of China. Moreover, it is rich in natural resources. Securinega suffruticosa Rehd. is a folk medicine whose root is the main component, with the effects of activating circulation, spleen, and stomach to treat rheumatism waist pain, limb numbness, infant malnutrition, and other diseases. The roots, stems, leaves, flowers, and skin of Securinega suffruticosa Rehd. contain alkaloids, in which securinine is the main ingredient.

Chemical Properties

YELLOW-BROWN OILY LIQUID AFTER MELTING

Physical properties

Appearance: yellow crystalline powder, slightly bitter. Solubility: soluble in anhydrous ethanol or chloroform, insoluble in water. Melting point: 139–140?°C Specific optical rotation: (D) ?1042°(C?=?1, EtOH).

History

Securinine was first isolated by a Soviet scholar from the Wusuli region, but its chemical structure was separated and finally determined by Chinese scholars from local sources . The main structural feature is a tetracyclic compound containing an indolizine, pyrrole elidine, or quinolizine ring and an α, β-unsaturated pentahydrin ring whose basic structural skeleton type is as shown in what follows .
Owing to the complexity of the chemical reaction of securinine, reports on its chemical reactivity and structural modification have been relatively scarce since securinine was reported on in 1956. However, the research on chemical total synthesis and biological activities of securinine has made a certain amount of progress.
Securinine has a rigid molecular structure containing four rings and three chiral centers, which makes synthesis difficult. From 1974 to 1978, three research groups from Japan, the USA, and Canada studied the biosynthesis of securinine by feeding animals with isotope-labeled S. suffruticosa.

Uses

This compound is a sensitizer.

Uses

3,4-Dinitrochlorobenzene is a useful reactant in organic synthesis.

Indications

Poliomyelitis sequela and facial paralysis, neurasthenia, hypotension, autonomic dysfunction, and others

Pharmacology

The pharmacological effect of securinine is mainly manifested as a central nervous system excitatory effect. As a GABA receptor inhibitor, it has an excitatory effect similar to that of strychnine on the spinal cord. A low dose of securinine can improve the excitability of brain reflection, while a high dose of securinine will cause febrile seizures, and at the same time securinine can strengthen the conditioned reflex of the cerebral cortex, shorten the latency period, and promote learning and memory capability , and so it is expected to be a promising drug for the treatment of Alzheimer’s disease.,
Securinine can improve the hematopoietic environment of patients with aplastic anemia, promote cell proliferation, have a synergistic anti-tumor effect in combination with cyclophosphamide (CTX), and can antagonize bone marrow suppression caused by CTX.?It has an inhibitory effect on cell proliferation of human leukocyte cell K562 and four other kinds of tumor cells.

Clinical Use

In recent years, securinine has been widely used in clinical practice, mainly for the treatment of polio sequelae and facial nerve palsy. It also has a certain effect on neurasthenia, hypotension and dizziness, tinnitus, and deafness caused by autonomic dysfunction. The nitrate and hydrochloride of left-handed securinine are mainly used clinically. In addition, securinine eye drops are found to have a remarkable effect on the treatment of herpes simplex keratitis through initial clinical observation.

3,4-Dinitrochlorobenzene Preparation Products And Raw materials

Global( 101)Suppliers
Supplier Tel Email Country ProdList Advantage
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49391 58
SIMAGCHEM CORP
+86-13806087780 sale@simagchem.com China 17367 58
Career Henan Chemica Co
+86-0371-86658258 15093356674; laboratory@coreychem.com China 30255 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671 sales@tnjchem.com China 34572 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com CHINA 52867 58
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923 1026@dideu.com China 9020 58
Hebei Duling International Trade Co. LTD
+8618712993135 sales01@hbduling.cn China 15741 58
Hebei Guanlang Biotechnology Co., Ltd.
+86-19930503259 +86-19930503259 cherry@crovellbio.com China 18451 58

View Lastest Price from 3,4-Dinitrochlorobenzene manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
3,4-Dinitrochlorobenzene pictures 2023-01-14 3,4-Dinitrochlorobenzene
610-40-2
US $20.00 / kg 1kg 99% 5000 tons Hebei Duling International Trade Co. LTD
4-Chloro-1,2-dinitrobenzen 4-CHLORO-1,2-DINITROBENZENE 3,4-DINITROCHLOROBENZENE 1-CHLORO-3,4-DINITROBENZENE 1-CHLORO-3,4-DINITROBENZENE, TECH., 90% Benzene, 4-chloro-1,2-dinitro- 1,2-Dinitro-5-chlorobenzene 1,2-Dinitro-4-chlorobenzene 1-Chloro-3,4-dinitrobenzene,90%,tech. 1-Chloro-3,4-dinitrobenzene, 92%+ 3,4-Dinitrochlorobenzene> Bendamustine Impurity 54 610-40-2 NO22C6H3Cl Building Blocks Nitrogen Compounds Organic Building Blocks Nitro Compounds Benzene derivates API intermediates Synthetic Flavours & Fragrances