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3-Acetoxyindole

Names

[ CAS No. ]:
608-08-2

[ Name ]:
3-Acetoxyindole

[Synonym ]:
1H-Indol-3-ol, acetate (ester)
MFCD00014561
EINECS 210-154-2
1H-Indol-3-yl acetate
acetic acid indol-3-yl ester
3-Indoxyl-3-acetate
Indol-3-ol, acetate (ester) (8CI)
Acetic acid, 3-indolyl ester
3-Acetoxyindole
Indoxyl acetate

Biological Activity

[Description]:

3-Indolyl acetate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
339.1±15.0 °C at 760 mmHg

[ Melting Point ]:
128-130 °C(lit.)

[ Molecular Formula ]:
C10H9NO2

[ Molecular Weight ]:
175.184

[ Flash Point ]:
158.9±20.4 °C

[ Exact Mass ]:
175.063324

[ PSA ]:
42.09000

[ LogP ]:
2.01

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

[ Index of Refraction ]:
1.634

[ Storage condition ]:
2-8°C

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
AI3325000
CHEMICAL NAME :
Acetic acid, 3-indolyl ester
CAS REGISTRY NUMBER :
608-08-2
BEILSTEIN REFERENCE NO. :
0143086
LAST UPDATED :
199701
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C10-H9-N-O2
MOLECULAR WEIGHT :
175.20
WISWESSER LINE NOTATION :
T56 BMJ DV1

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 :
600 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
NYKZAU Nippon Yakurigaku Zasshi. Japanese Journal of Pharmacology. (Nippon Yakuri Gakkai, c/o Kyoto Daigaku Igakubu Yakurigaku Kyoshitsu, Konoe-cho, Yoshida, Sakyo-ku, Kyoto 606, Japan) V.40- 1944- Volume(issue)/page/year: 55,1514,1959 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X2616 No. of Facilities: 178 (estimated) No. of Industries: 1 No. of Occupations: 4 No. of Employees: 663 (estimated) No. of Female Employees: 550 (estimated)

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

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

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

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

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
R22

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
AI3325000

[ HS Code ]:
2933990090

Synthetic Route

Precursor & DownStream

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

Comparison of three rapid methods, tributyrine, 4-methylumbelliferyl butyrate, and indoxyl acetate, for rapid identification of Moraxella catarrhalis.

J. Clin. Microbiol. 32(5) , 1362-3, (1994)

Moraxella catarrhalis can easily be differentiated from other oxidase-positive, gram-negative cocci with tributyrine, 4-methylumbelliferyl butyrate, or indoxyl acetate. All M. catarrhalis give positiv...

Arcobacter mytili sp. nov., an indoxyl acetate-hydrolysis-negative bacterium isolated from mussels.

Int. J. Syst. Evol. Microbiol. 59 , 1391-1396, (2009)

Three Arcobacter isolates, recovered from mussels (genus Mytilus), and one isolate from brackish water in Catalonia (north-east Spain) showed a novel pattern using a recently described identification ...

Arcobacter molluscorum sp. nov., a new species isolated from shellfish.

Syst. Appl. Microbiol. 34 , 105-109, (2011)

Nineteen bacteria isolates recovered from shellfish samples (mussels and oysters) showed a new and specific 16S rDNA-RFLP pattern with an Arcobacter identification method designed to recognize all spe...


More Articles


Related Compounds

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