2,3-Diaminophenol

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
303.6±27.0 °C at 760 mmHg

[ Melting Point ]:
161-165 °C(lit.)

[ Molecular Formula ]:
C₆H₈N₂O

[ Molecular Weight ]:
124.141

[ Flash Point ]:
137.4±23.7 °C

[ Exact Mass ]:
124.063660

[ PSA ]:
72.27000

[ LogP ]:
-0.30

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.723

[ Storage condition ]:
2-8°C

Click to get detail MSDS

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H332-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful;

[ Risk Phrases ]:
R20/22;R36/37/38

[ Safety Phrases ]:
S26

[ RIDADR ]:
UN 3259 8/PG 2

[ WGK Germany ]:
3

[ HS Code ]:
2922299090

Precursor

DownStream

[ HS Code ]: 2922299090

[ Summary ]:
2922299090. other amino-naphthols and other amino-phenols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

1,5-Benzoxazepines vs 1,5-benzodiazepines. one-pot microwave-assisted synthesis and evaluation for antioxidant activity and lipid peroxidation inhibition.

J. Med. Chem. 53(23) , 8409-20, (2010)

Amino-1,5-benzoxazepines 2 and 5 and hydroxyl-1,5-benzodiazepines 3 and 6 have been synthesized in one-pot solvent-free conditions from 2,3-diaminophenol and ketones through microwave assisted acid ca...

Pd(II) and Pt(II) complexes with aromatic diamines: study of their interaction with DNA.

J. Inorg. Biochem. 98(3) , 510-21, (2004)

Pd(II) and Pt(II) new complexes with simple aromatic diamines were synthesised and characterised with the aim of studying their possible antitumour activity. The aromatic diamines chosen were 2,3-diam...

On benzo[b][1,4]diazepinium-olates, -thiolates and -carboxylates as anti-Hückel mesomeric betaines.

Org. Biomol. Chem. 1(23) , 4342-50, (2003)

2,3-Diaminophenol 4, 3,4-diaminophenol 5, 4-methoxy-1,2-diaminobenzene 6, 3,4-diaminobenzenethiol 7, 2,3-diaminobenzoic acid 8, and 3,4-diaminobenzoic acid 9 were reacted with 2,4-pentanedione to yiel...

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