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1,1'-Azobis(cyanocyclohexane)

CAS No.
2094-98-6
Chemical Name:
1,1'-Azobis(cyanocyclohexane)
Synonyms
ACCN;V-40;1,1'-Azobis(cyclohexanecarbonitrile);MDEG;BNAC1;ASIC2;LABOTEST-BB LT00160148;AZO-1-CYANOCYCLOHEXANE;Azodicyclohexanonitrile;1-Azo-1-cyanocyclohexane
CBNumber:
CB8687740
Molecular Formula:
C14H20N4
Molecular Weight:
244.34
MDL Number:
MFCD00046334
MOL File:
2094-98-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 05:03:46

1,1'-Azobis(cyanocyclohexane) Properties

Melting point 114-118 °C(lit.)
Boiling point 423.9±38.0 °C(Predicted)
Density 1.13±0.1 g/cm3(Predicted)
vapor pressure 0-0.001Pa at 20-25℃
storage temp. 2-8°C
form Solid:crystalline
BRN 960744
Stability Stable, but decomposes exothermically above about 114 C
InChI 1S/C14H20N4/c15-11-13(7-3-1-4-8-13)17-18-14(12-16)9-5-2-6-10-14/h1-10H2/b18-17+
InChIKey KYIKRXIYLAGAKQ-ISLYRVAYSA-N
SMILES N#CC1(CCCCC1)\N=N\C2(CCCCC2)C#N
LogP 3.256 at 25℃ and pH5-6
CAS DataBase Reference 2094-98-6(CAS DataBase Reference)
FDA UNII 9Y0B93KKUS
EPA Substance Registry System 1,1'-Azobiscyclohexanecarbonitrile (2094-98-6)
UNSPSC Code 12162002
NACRES NA.23

SAFETY

Risk and Safety Statements

Symbol(GHS)  Flame (GHS02)Exclamation Mark (GHS07)Environment (GHS09)
GHS02,GHS07,GHS09
Signal word  Danger
Hazard statements  H242-H332-H335-H411
Precautionary statements  P210-P234-P235-P240-P280-P261-P271-P273-P370+P378-P304+P340-P312-P391-P403-P411-P420-P403+P233-P405-P501
target organs Respiratory system
PPE Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  F,Xi
Risk Statements  11-36/37/38
Safety Statements  26
RIDADR  UN 3226 4.1
WGK Germany  3
4.9
TSCA  TSCA listed
HazardClass  4.1
PackingGroup  II
Storage Class 5.2 - Organic peroxides and self-reacting hazardous materials
Hazard Classifications Eye Irrit. 2
Self-react. D
Skin Irrit. 2
STOT SE 3
REACH Registrations Active
Limited Quantities 1.0 Kg (2.2 lbs)
Excepted Quantities Not Permitted as Excepted Quantity

1,1'-Azobis(cyanocyclohexane) price More Price(13)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 380210 1,1′-Azobis(cyclohexanecarbonitrile) 98% 2094-98-6 25g $71.1 2026-04-30 Buy
Sigma-Aldrich 380210 1,1′-Azobis(cyclohexanecarbonitrile) 98% 2094-98-6 100g $193 2026-04-30 Buy
Usbiological 555716 ASIC2 PurifiedbyProteinGaffinitychromatography. 50ug $509 2026-06-03 Buy
Usbiological 555716 ASIC2 PurifiedbyProteinGaffinitychromatography. 100ug $708 2026-06-03 Buy
Usbiological 259931 1,1'-Azobis(cyclohexane-1-carbonitrile Asreported 2094-98-6 10g $333 2026-06-03 Buy
Product number Packaging Price Buy
380210 25g $71.1 Buy
380210 100g $193 Buy
555716 50ug $509 Buy
555716 100ug $708 Buy
259931 10g $333 Buy

1,1'-Azobis(cyanocyclohexane) Chemical Properties, Uses, Production

Chemical Properties

faintly beige crystalline powder

Uses

A more efficient radical initiator than AIBN has been employed to initiate primary radical reactions.

Synthesis Reference(s)

Journal of the American Chemical Society, 71, p. 2661, 1949 DOI: 10.1021/ja01176a018
Organic Syntheses, Coll. Vol. 4, p. 66, 1963

General Description

A white to light colored solid substance. Insoluble in water and more dense that water. May cause irritation to skin, eyes, and mucous membranes. May be toxic by ingestion. If exposed to high temperatures or flames 1,1'-Azobis(cyanocyclohexane) may ignite and burn with an intense flame. Dust may form an explosive mixture in air.

Air & Water Reactions

Dust may form an explosive mixture in air. Insoluble in water.

Reactivity Profile

Self-decomposition or self-ignition may be triggered by heat, chemical reaction, friction or impact. May be ignited by heat, sparks or flames. 1,1'-Azobis(cyanocyclohexane) is an azo compound. Azo, diazo, azido compounds can detonate. This applies in particular to organic azides that have been sensitized by the addition of metal salts or strong acids. Toxic gases are formed by mixing materials of this class with acids, aldehydes, amides, carbamates, cyanides, inorganic fluorides, halogenated organics, isocyanates, ketones, metals, nitrides, peroxides, phenols, epoxides, acyl halides, and strong oxidizing or reducing agents. Flammable gases are formed by mixing materials in this group with alkali metals. Explosive combination can occur with strong oxidizing agents, metal salts, peroxides, and sulfides.

Health Hazard

Fire may produce irritating and/or toxic gases. Contact may cause burns to skin and eyes. Contact with molten substance may cause severe burns to skin and eyes. Runoff from fire control may cause pollution.

Fire Hazard

Flammable/combustible material. May be ignited by friction, heat, sparks or flames. Some may burn rapidly with flare burning effect. Powders, dusts, shavings, borings, turnings or cuttings may explode or burn with explosive violence. Substance may be transported in a molten form at a temperature that may be above its flash point. May re-ignite after fire is extinguished.

Purification Methods

Purify the nitrile by dissolving it in boiling 95%EOH as rapidly as possible, cool overnight at 0o, filter, wash with a little EtOH and dry it in a vacuum desiccator over CaCl2. Note that prolonged heating >80o causes decomposition. Recrystallise it from EtOH. It should be regarded as potentially explosive. It is a radical initiator. [Overberger et al. Org Synth Coll Vol IV 66 1963, Beilstein 16 II 97.]

1,1'-Azobis(cyanocyclohexane) Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 83)
Supplier Tel Email Country ProdList Advantage
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Shanghai Hanhong Scientific Co.,Ltd. 021-54306202 13764082696 info@hanhongsci.com China 42917 64
Shandong Xiya Chemical Co., Ltd 13355009207 13355009207 3007715519@qq.com China 18722 57
Sichuan Kulinan Technology Co., Ltd 400-1166-196 18981987031 cdhxsj@163.com China 11674 57
Sinopharm Chemical Reagent Co,Ltd. 86-21-63210123 sj_scrc@sinopharm.com China 9791 79
9ding chemical ( Shanghai) Limited 4009209199 sales@9dingchem.com China 22497 55
The future of Shanghai Industrial Co., Ltd. 021-61552785 sales@shshiji.com China 9531 55
Shanghai Ruji Biology Technology Co., Ltd. +86-21-65211385-8001 36031160 sales@shruji.com China 3223 55
Wuxi Zhangkun Biochemical Technology Co., Ltd. +86 0510-85629785 China 2321 58
Quzhou Juhua Friendship Co., Ltd 0570-3066667 China 3922 58

View Latest Price from 1,1'-Azobis(cyanocyclohexane) manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
1,1 2021-07-02 1,1"-Azobis(cyclohexanecarbonitrile) 98%
2094-98-6
$10.00-15.00 1KG 99%+ HPLC Zhuozhou Wenxi import and Export Co., Ltd
1,1'-Azobis(cyanocyclohexane) pictures 2020-01-03 1,1'-Azobis(cyanocyclohexane)
2094-98-6
$6.60 1KG 97%-99% 1kg -1000kg Career Henan Chemical Co
1,1’-azobis-cyclohexanecarbonitril 1,1'-azobis(cyclohexanebenzonitrile) ANTI-ACCN1 (CENTER) antibody produced in rabbit ASIC2 BNAC1 MDEG 1,1′-Azobis(cyanocyclohexane), ACHN, VAZO catalyst 88 free radical source Azodicyclohexanonitrile 1,1'-AZODICYCLOHEXANE CARBONITRILE 1,1′-Azodi-(hexahydrobenzonitrile) 1,1'-AZOBIS(CYCLOHEXANE-1-CARBONITRILE) 1,1'-AZOBIS CYANOCYCLOHEXANE LABOTEST-BB LT00160148 AZO-1-CYANOCYCLOHEXANE VAZO(R) CATALYST 88 FREE RADICAL SOURCE VAZO? catalyst 88 free radical source 1,1'-azobis(1-cyclohexanecarbonitrile) 1,1'-AZOBIS(CYCLOHEXANECARBONITRILE), 98 % Azobis-(1-cyclohexanecarbonitrile) Cyclohexanecarbonitrile, 1,1-azobis- 1,1''-Azobis-(1-cyanocyclohexane) 1,1-AZODICYCLOHEXANECARBONITRILE 98% 1,1’-Azobis(cyclohexane-1-carbonitrile) (V-40) 1,1μ-Azobis(cyanocyclohexane), VAZO(R) catalyst 88 free radical source 1-(1-Cyanocyclohexyl)diazenylcyclohexane-1-carbonitrile 1-Azo-1-cyanocyclohexane Azo-(1,1-hexahydrobenzonitrile) N,N-Azobis(cyclohexanecarbonitrile) 1-(1-cyanocyclohexyl)azocyclohexanecarbonitrile 1,1'-Azabis[cyclohexenecarbonitrile) 2094-98-6 C14H20N4 1,1'-Azobis(cyanocyclohexane) 1,1-azobis(cyanocyclohexanecarbonitrile) 1,1'-Azobis(cyanocyclohexane) 1,1'-Azodi(hexahydrobenzonitrile) 1,1'-Azodicyclohexanecarbonitrile 1,1'-Azobis(cyclohexanecarbonitrile) ACCN V-40 2094-98-6 NCC6H10NNC6H10CN Radical Chemistry Radical Initiators Synthetic Reagents