Chemical Properties Usage Usage limitation Preparation Content analysis Category Toxicity grade Toxicity Acute toxicity Stimulus data Flammability hazard characteristics Storage Fire extinguishing agent
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Isoquinoline

Chemical Properties Usage Usage limitation Preparation Content analysis Category Toxicity grade Toxicity Acute toxicity Stimulus data Flammability hazard characteristics Storage Fire extinguishing agent
Product Name
Isoquinoline
CAS No.
119-65-3
Chemical Name
Isoquinoline
Synonyms
LEUCOLINE;FEMA 2978;IsoquinoL;ISOQUINOLIN;2-Benzanine;ISOCHINOLIN;2-BENZAZINE;ISOQINOLINE;ISOQUINOLINE;Isochinoline
CBNumber
CB1690422
Molecular Formula
C9H7N
Formula Weight
129.16
MOL File
119-65-3.mol
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Isoquinoline Property

Melting point:
26-28 °C (lit.)
Boiling point:
242-243 °C (lit.)
Density 
1.099 g/mL at 25 °C (lit.)
FEMA 
2978 | ISOQUINOLINE
refractive index 
n20/D 1.623(lit.)
Flash point:
225 °F
storage temp. 
2-8°C
solubility 
5g/l
pka
5.42(at 20℃)
form 
Low Melting Solid
color 
Light brown
PH
7.5 (5g/l, H2O, 20℃)
Water Solubility 
practically insoluble
JECFA Number
1303
Merck 
14,5222
BRN 
107549
InChIKey
AWJUIBRHMBBTKR-UHFFFAOYSA-N
CAS DataBase Reference
119-65-3(CAS DataBase Reference)
NIST Chemistry Reference
Isoquinoline(119-65-3)
EPA Substance Registry System
Isoquinoline (119-65-3)
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Safety

Hazard Codes 
T
Risk Statements 
22-24-38-52/53-36/38-21/22-45
Safety Statements 
36/37-45-36/37/39-61-53
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
2
RTECS 
NW6825000
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
II
HS Code 
29334900
Toxicity
LD50 orally in rats: 360 mg/kg (Smyth)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H302Harmful if swallowed

H311Toxic in contact with skin

H315Causes skin irritation

H319Causes serious eye irritation

H350May cause cancer

H412Harmful to aquatic life with long lasting effects

Precautionary statements

P201Obtain special instructions before use.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P273Avoid release to the environment.

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

P321Specific treatment (see … on this label).

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.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
282162
Product name
Isoquinoline
Purity
technical grade, 90-92%
Packaging
100ml
Price
$51.2
Updated
2021/03/22
Sigma-Aldrich
Product number
68853
Product name
Isoquinoline
Purity
analytical standard
Packaging
1ml
Price
$62.7
Updated
2020/08/18
TCI Chemical
Product number
I0182
Product name
Isoquinoline
Purity
>95.0%(GC)
Packaging
25g
Price
$22
Updated
2021/03/22
TCI Chemical
Product number
I0182
Product name
Isoquinoline
Purity
>95.0%(GC)
Packaging
500g
Price
$124
Updated
2021/03/22
Alfa Aesar
Product number
B21279
Product name
Isoquinoline, 97%
Packaging
100g
Price
$63.6
Updated
2021/03/22
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Isoquinoline Chemical Properties,Usage,Production

Chemical Properties

Colorless flaky crystal or liquid, similar fragrance to bitter almonds and Chervil, sweet taste, melting point 23℃,boiling point 243℃, soluble in ethanol and non-volatile oil, diluted inorganic acid and most organic solvents, slightly soluble in water.

Usage

  • A kind of Spice
  • Mainly used for the preparation of vanilla spice.   
  • Used in the production of pesticides, medicine, rubber accelerator, color film sensitizing agent, dyes, anion exchange resin and so on.
  • Used as gas chromatographic stationary liquid and analytical reagent,
  • Used in the pharmaceutical industry.
  • Used for the production of drugs for prevention and treatment of schistosomiasis (praziquantel), antimalarial, chemical reagents, etc.
  • Isoquinoline can be oxidized to produce Pyridine carboxylic acid And Its derivatives can be used for the production of color films and dyes.  It can be used as Iron preservative, soluble phenolic resin curing agent, etc. Its Addition compounds formed with metals can be used for the quantitative determination of nickel and cadmium and the qualitative determination of noble metal. Isoquinoline can also be used as a catalyst in the benzoylation reaction and polymerization of α-olefin.

Usage limitation

FEMA(mg/kg): Soft drinks 0.25,, cold drinks 0.25, sweets1.0; bakery products 0.004-1.0, moderate use (FDA§172.515,2000).

Preparation

Crude quinoline containing 83% quinoline, 15% isoquinoline and 2% methyl quinoline can be used as the raw material for the production of isoquinoline. However, the Distillation section from 237.5-239.5℃ and 243-246℃ is generally collected and used as the raw material for the extraction of isoquinoline. 13-28% of 2-methyl quinoline and 3.9% quinoline can be separated from this distillation section in the form of hydrochloride salt.
The isoquinoline fraction reacted with 98% sulfuric acid at 35℃ in alcohol solution to produce isoquinoline sulfonate. Isoquinoline sulfonate crystallizes faster than its homologues in the cooling process. After filtration, recrystallization was carried out with 85% ethanol, and then decomposed with 20% ammonia water. The generated oil layer was firstly washed with water, and then rectified to collect the fraction at242-243℃to obtain Isoquinoline with purity greater than 95%  It is separated by repeated freezing the coal tar with the boiling rangeat 238~250℃.

Content analysis

Determined by Gas chromatography and liquid chromatography and the chromatographic test conditions are the same as α-allyl ionone (03411).

Category

flammable liquid

Toxicity grade

middle toxic

Toxicity

GRAS(FEMA)

Acute toxicity

Oral – rat LD50: 360mg/kg

Stimulus data

Skin-rabbit  10 mg/24h mild;  eye-rabbit 250 μg severe.

Flammability hazard characteristics

Flammable in case of fire, high temperature and oxidants, Combustion produces toxic nitrogen oxide smog.

Storage

Completely packed, handle with care; Ventilated warehouse, away from open flame, high temperature, separated from strong acids.

Fire extinguishing agent

foam, carbon dioxide, dry powder, dry sand, water spray.

Description

Isoquinoline has an odor reminiscent of benzaldehyde and anise. Isoquinoline may be obtained from coal tar (238 - 250°C boiling fraction); it is isolated as the sulfate or as is by repeated freezing.

Chemical Properties

Isoquinoline has a heavy sweet balsamic, herbaceous odor.

Chemical Properties

LIGHT BROWN LOW MELTLING SOLID

Occurrence

Reported found in milk and dried bonito; also occurs in coal tar, where it is formed during the dry distillation of coal

Uses

Manufacture of pharmaceuticals (such as nicotinic acid), dyes, insecticides, rubber accelerators, and in organic synthesis.

Uses

It is used in the manufacture of dyes, pharmaceuticals,and insecticides, and as an antimalarialagent.

Preparation

Obtained from coal tar (238 to 250°C boiling fraction); it is isolated as the sulfate or as is by repeated freezing

Definition

ChEBI: An ortho-fused heteroarene that is a benzopyridine in which the N atom not directly attached to the benzene ring.

Synthesis Reference(s)

The Journal of Organic Chemistry, 29, p. 2240, 1964 DOI: 10.1021/jo01031a031
Synthesis, p. 288, 1974

Hazard

Toxic by ingestion.

Health Hazard

The toxic properties of this compound aresimilar to those of quinoline. It is moderatelytoxic in rats and rabbits by oral routeand skin absorption. The oral LD50 value inrats is 360 mg/kg. The irritation effects onskin and eyes in rabbits were moderate tosevere. Carcinogenicity due to isoquinolinein animals or humans is not known. The histidinereversion–Ames test for mutagenicitywas inconclusive.

Fire Hazard

Noncombustible liquid (solid).

Purification Methods

Dry isoquinoline with Linde type 5A molecular sieves or Na2SO4 and fractionally distil at reduced pressure. Alternatively, it can be refluxed with, and distilled from, BaO. It is also purified by fractional crystallisation from the melt and distilled from zinc dust. It forms a phosphate (m 135o) and a picrate (m 223o), which are purified by crystallisation, and the free base can be recovered and distilled. [Packer et al. J Am Chem Soc 80 905 1958.] The procedure for purification via the picrate comprises the addition of quinoline to picric acid dissolved in the minimum volume of 95% EtOH to yield yellow crystals which are washed with EtOH and air dried before recrystallising from acetonitrile. The crystals are dissolved in dimethyl sulfoxide (previously dried over 4A molecular sieves) and passed through a basic alumina column, on which picric acid is adsorbed. The free base in the effluent is extracted with n-pentane and distilled under vacuum. Traces of solvent from small quantities are removed by vapour phase chromatography. The hydrochloride crystallises from EtOH with m 193o. [Mooman & Anton J Phys Chem 80 2243 1976, Beilstein 20 II 236, 20 III/IV 3410, 20/7 V 333.]

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Isoquinoline Suppliers

Anshan Beida Industrial Co., Ltd.
Tel
86-0412-8410999
Email
13904227333@126.com
Country
China
ProdList
1
Advantage
58
Tocopharm Co., Ltd.
Tel
021-69895597- ;021-69895597- ;021-69895597-
Fax
021-61292409
Email
info@tocopharm.com;sales@tocopharm.com;739486509@qq.com
Country
China
ProdList
208
Advantage
55
Hangzhou YiDi Industrial Co., Ltd.
Tel
0571-82609104-
Fax
0571-82691158
Email
yidipharma@163.com
Country
China
ProdList
117
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833- ;010-82848833-
Fax
86-10-82849933
Email
jkinfo@jkchemical.com;market6@jkchemical.com
Country
China
ProdList
96500
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
21-61259100-
Fax
86-21-61259102
Email
sh@meryer.com
Country
China
ProdList
40264
Advantage
62
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15877
Advantage
69
Alfa Aesar
Tel
400-610-6006; 021-67582000
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30159
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386 / 800-988-0390
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24555
Advantage
81
ShangHai DEMO Chemical Co.,Ltd
Tel
400-021-7337 qq:2355568890
Fax
0086-21-50182339
Email
sales@demochem.com; export1@demochem.com
Country
China
ProdList
2582
Advantage
57
Beijing dtftchem Technology Co., Ltd.
Tel
13651141086; 86(10)60275028、60275820
Fax
86 (10) 60270825
Email
dtftchem@sina.com
Country
China
ProdList
3392
Advantage
62
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View Lastest Price from Isoquinoline manufacturers

Hebei Guanlang Biotechnology Co., Ltd.
Product
Isoquinoline 119-65-3
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2021-08-19
Hebei Dongdu Import and Export Co. LTD
Product
isoquinoline 119-65-3
Price
US $60.00/g
Min. Order
500g
Purity
99%
Supply Ability
20 tons
Release date
2020-11-27
Shaanxi Dideu Medichem Co. Ltd
Product
Isoquinoline 119-65-3
Price
US $0.00-0.00/KG
Min. Order
1g
Purity
99%
Supply Ability
2000tons
Release date
2019-12-31

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