5-Indolol

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Names

[ CAS No. ]:
1953-54-4

[ Name ]:
5-Indolol

[Synonym ]:
5-hydroxyindol
5-Hydroxyindole,5-Indolol
5-hydroxy-1H-indol
EINECS 217-782-6
1H-Indol-5-ol
5-Hydroxy-1H-indole
INDOL-5-OL
1H-indole-5-ol
Hydroxy-5-indole
5-Indolol
5-hydroxylindole
5-hydroxy-indole
5-Hydroxyindole
MFCD00005677
MFCD0005677

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
343.2±15.0 °C at 760 mmHg

[ Melting Point ]:
105-110ºC

[ Molecular Formula ]:
C8H7NO

[ Molecular Weight ]:
133.147

[ Flash Point ]:
161.4±20.4 °C

[ Exact Mass ]:
133.052765

[ PSA ]:
36.02000

[ LogP ]:
0.97

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.739

[ Storage condition ]:
0-6°C

MSDS

Click to get detail MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
NM2430000
CHEMICAL NAME :
Indol-5-ol
CAS REGISTRY NUMBER :
1953-54-4
BEILSTEIN REFERENCE NO. :
0112349
LAST UPDATED :
199612
DATA ITEMS CITED :
2
MOLECULAR FORMULA :
C8-H7-N-O
MOLECULAR WEIGHT :
133.16
WISWESSER LINE NOTATION :
T56 BMJ GQ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
EJMCA5 European Journal of Medicinal Chemistry--Chimie Therapeutique. (Editions Scientifiques Elsevier, 29 rue Buffon, F-75005, Paris, France) V.9- 1974- Volume(issue)/page/year: 9,453,1974
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
56 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
CSLNX* U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. (Aberdeen Proving Ground, MD 21010) Volume(issue)/page/year: NX#01920

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

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

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

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
NM2430000

[ HS Code ]:
29339990

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 1-[2-(5-Benzyloxy-2-nitrophenyl)vinyl]pyrrolidine
  • 5-Benzyloxyindole
  • 5-Methoxyindole
  • 5-(prop-2-ynynloxy)indole
  • (4-BENZYLOXY-PHENYL)-HYDRAZINE
  • Indole
  • 4-Nitrophenol
  • 1-Benzyloxy-4-Nitrobenzene

DownStream

  • 5-HYDROXY-DL-TRYPTOPHAN ETHYL ESTER HYDROCHLORIDE
  • 5-Hydroxy-1H-indole-3-carbaldehyde
  • BRL-54443
  • 1-(4-METHYLBENZENESULFONYL)-1H-INDOLE
  • 5-Hydroxyanthranilic acid
  • N-Boc-5-Hydroxyindole
  • TERT-BUTYL ((1H-INDOL-5-YL)METHYL)CARBAMATE
  • 5-hydroxy-1H-indazole-3-carbaldehyde
  • 4-Tolylmethylcarbinol
  • 3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indol-5-ol

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Validation and application of an UPLC-MS/MS method for the quantification of synthetic cannabinoids in urine samples and analysis of seized materials from the Portuguese market.

Forensic Sci. Int. 243 , 117-25, (2014)

An UPLC-MS/MS method using ESI+ionization and MRM was developed and fully validated according to international guidelines for the qualitative and quantitative analysis of nine synthetic cannabinoids a...

A separation of tyramine on a 2-(4-methoxyphenyl)ethylamine imprinted polymer: an answer from theoretical and experimental studies.

Talanta 129 , 155-64, (2014)

A 2-(4-methoxyphenyl)ethylamine imprinted polymer (MIP) was successfully applied for the selective separation of tyramine. A computational analysis was used to predict the affinity of the polymer matr...

Determination of selected synthetic cannabinoids and their metabolites by micellar electrokinetic chromatography--mass spectrometry employing perfluoroheptanoic acid-based micellar phase.

Talanta 150 , 568-76, (2016)

Perfluoroheptanoic acid was employed as a volatile micellar phase in background electrolyte for micellar electrokinetic chromatography-tandem mass spectrometry separation and determination of 15 selec...


More Articles

Related Compounds

  • 3-(2-Aminopropyl)-5-indolol hydrochloride
  • 5-(2,4-difluorophenyl)-2-hydroxy-3-sulfooxybenzoic acid
  • 5-hydroxy-3-(methylamino)naphthalene-2,7-disulfonic acid
  • 5-methoxy-3-(di-n-propylamino)chroman
  • 5-BROMO-2,3-DIHYDRO-1H-INDOLE HYDROCHLORIDE
  • 5-(p-Toluenesulfonate)-2,3-O-isopropylidene-2-C-methyl-D-ribonic-gamma-lactone
  • 4-(Propan-2-yl)pyrrolidin-3-ol
  • N-(1-cyanocyclopentyl)-2-[5-oxo-3-(pyridin-2-yl)-4,5-dihydro-1,2,4-oxadiazol-4-yl]acetamide
  • N-[3-(3-methoxyphenyl)-1,2,4-thiadiazol-5-yl]furan-2-carboxamide
  • 2-{[1-(Hydroxymethyl)cyclopentyl]amino}-2-methylpropan-1-ol
  • 2,2,2-Trifluoro-1-[3-(2-methylpropyl)imidazo[1,5-a]pyridin-1-yl]ethan-1-one
  • 4-(4-(Benzyloxy)phenyl)-1h-pyrazole
  • 4-[(2,6-Dichloropyrimidin-4-yl)amino]cyclohexan-1-ol
  • Ethyl 2-amino-4-(2'-hydroxy-[1,1'-biphenyl]-4-yl)thiophene-3-carboxylate
  • 6-(propan-2-yl)-1H,2H,3H-pyrrolo[2,3-b]quinoline
  • N-benzyl-N-methyl-6-nitropyridin-3-amine
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