| Identification | More | [Name]
2-NITROPHENYL ISOCYANATE | [CAS]
3320-86-3 | [Synonyms]
2-NITROPHENYL ISOCYANATE O-NITROPHENYL ISOCYANATE TIMTEC-BB SBB006627 1-isocyanato-2-nitro-benzen 1-Isocyanato-2-nitrobenzene Benzene, 1-isocyanato-2-nitro- Isocyanic acid, o-nitrophenyl ester 2-Isocyanatonitrobenzene 2-NITROPHENYL ISOCYANATE 97% | [EINECS(EC#)]
222-024-2 | [Molecular Formula]
C7H4N2O3 | [MDL Number]
MFCD00007092 | [Molecular Weight]
164.12 | [MOL File]
3320-86-3.mol |
| Chemical Properties | Back Directory | [Appearance]
yellow crystalline solid | [Melting point ]
40-41 °C(lit.) | [Boiling point ]
135-137 °C17 mm Hg(lit.) | [density ]
1.5018 (rough estimate) | [refractive index ]
1.5300 (estimate) | [Fp ]
>230 °F
| [storage temp. ]
Refrigerator (+4°C) | [form ]
Crystalline Solid | [color ]
Yellow | [InChI]
1S/C7H4N2O3/c10-5-8-6-3-1-2-4-7(6)9(11)12/h1-4H | [InChIKey]
JRVZITODZAQRQM-UHFFFAOYSA-N | [SMILES]
[O-][N+](=O)c1ccccc1N=C=O | [CAS DataBase Reference]
3320-86-3(CAS DataBase Reference) | [EPA Substance Registry System]
Benzene, 1-isocyanato-2-nitro- (3320-86-3) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S27:Take off immediately all contaminated clothing . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [RIDADR ]
2206 | [WGK Germany ]
3
| [TSCA ]
TSCA listed | [HazardClass ]
6.1(b) | [PackingGroup ]
III | [HS Code ]
29291090 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Acute Tox. 4 Dermal Acute Tox. 4 Inhalation Acute Tox. 4 Oral Eye Irrit. 2 Resp. Sens. 1 Skin Irrit. 2 Skin Sens. 1 STOT SE 3 |
| Hazard Information | Back Directory | [Chemical Properties]
yellow crystalline solid | [Uses]
2-Nitrophenyl isocyanate was used in the synthesis of symmetrical bis-2-nitrophenylcarbodi-imide via dimerisation reaction. |
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SVH BIOSCIENCES
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