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Suppliers for

Isatin

Properties

CAS   91-56-5 
Formula   C8H5NO2 
EINECS   202-077-8 

Structure

23 Registered suppliers

rd Simagchem Corporation P.R.China
rd Aecochem Corp. P.R.China
rd Sancai Industry Co.,Ltd. P.R.China
rd H&Z Industry Co.,Ltd P.R.China
rd Xingrui Industry Co., Limited P.R.China
rd Leap Chem Co., Ltd P.R.China CD details
rd Richman Chemical Inc., USA
Molecular Formula: C8H5NO2
Molecular Weight: 147.1308

rd Klaus F. Meyer GmbH Germany
Molecular Formula: C8H5NO2
Molecular Weight: 147.1308

rd Krada CPS Industry S.L Spain
Molecular Formula: C8H5NO2
Molecular Weight: 147.1308

rd Shandong Minglang Chemical Co., Ltd P.R.China
Molecular Formula: C8H5NO2
Molecular Weight: 147.1308

rd Lori Industry Co., Ltd P.R.China
Molecular Formula: C8H5NO2
Molecular Weight: 147.1308

rd Zehao Industry Co., Ltd. P.R.China CD details
rd Finetech Industry Limited P.R.China CD details
rd Hangzhou Lingrui Chemical Co., Ltd. P.R.China


More details are to be found here
rd Skyrun Industrial Co., Ltd. P.R.China


More details are to be found here
rd Ambeed, Inc. USA CD details
rd Xiamen Equation Chemical Co.,Ltd P.R.China
Purity : 98%
Smile code : O=C1NC2=C(C=CC=C2)C1=O
MDL Number : MFCD00005718
MolFormula : C8H5NO2
MolWeight : 147.1308
Available in stock : 134475.895

More details are to be found here
rd AK Scientific, Inc. USA
Purity : 98%
Smile code : O=C1NC2=C(C=CC=C2)C1=O
MDL Number : MFCD00005718
MolFormula : C8H5NO2
MolWeight : 147.1308
Available in stock : 134475.895

More details are to be found here
rd BuGuCh & Partners Germany CD details
rd Fabrichem, Inc. USA
Product Name: Isatin
Synonyms: TIMTEC-BB SBB009100;O-AMINOPHENYLGLYOXALIC LACTIM;O-AMINOBENZOYLFORMIC ACID;O-AMINOBENZOYLFORMIC ANHYDRIDE;AKOS BBS-00003223;2,3-DIKETOINDOLINE;2,3-DIHYDROINDOLE-2,3-DIONE;2,3-INDOLEDIONE
CAS: 91-56-5
MF: C8H5NO2
MW: 147.13
EINECS: 202-077-8
mp 193-195 °C (dec.)(lit.)
Fp 220 °C
storage temp. Store at RT.
Decomposition 194 ºC
Merck 14,5104
BRN 383659
Stability: Stable. Incompatible with strong acids.

chemical property: orange-red powder or crystals

Uses
Indigo and its derivatives as indigo and related dyes and some of the raw materials for the preparation of drugs. Because of its hepatotoxicity, indigo derivatives are no longer used in the pharmaceutical industry.
A precipitant for the detection of ketones and silver. Spectrophotometric Determination of Thiophene, Thiol, Thiophene, Urine Blue and Proline.

Preparation Source
By indophenol or indigo by oxidation and prepared. Indigo was first isolated by the French chemist Auguste Laurent. In 1878, Adolf von Bayer completed the full synthesis of isatin. In 1880, Bayer developed a method of synthesizing isatin from o-nitrocinnamic acid. In 1883, from the o-nitrobenzaldehyde synthesis of isatin method by Bayer patent. Since then, indigo as the raw material for the synthesis of indigo gradually replace the method of extraction from plants, as the main source of indigo.

rd BASF Belgium S.A. / N.V. Belgium
Product Name: Isatin
Synonyms: TIMTEC-BB SBB009100;O-AMINOPHENYLGLYOXALIC LACTIM;O-AMINOBENZOYLFORMIC ACID;O-AMINOBENZOYLFORMIC ANHYDRIDE;AKOS BBS-00003223;2,3-DIKETOINDOLINE;2,3-DIHYDROINDOLE-2,3-DIONE;2,3-INDOLEDIONE
CAS: 91-56-5
MF: C8H5NO2
MW: 147.13
EINECS: 202-077-8
mp 193-195 °C (dec.)(lit.)
Fp 220 °C
storage temp. Store at RT.
Decomposition 194 ºC
Merck 14,5104
BRN 383659
Stability: Stable. Incompatible with strong acids.

chemical property: orange-red powder or crystals

Uses
Indigo and its derivatives as indigo and related dyes and some of the raw materials for the preparation of drugs. Because of its hepatotoxicity, indigo derivatives are no longer used in the pharmaceutical industry.
A precipitant for the detection of ketones and silver. Spectrophotometric Determination of Thiophene, Thiol, Thiophene, Urine Blue and Proline.

Preparation Source
By indophenol or indigo by oxidation and prepared. Indigo was first isolated by the French chemist Auguste Laurent. In 1878, Adolf von Bayer completed the full synthesis of isatin. In 1880, Bayer developed a method of synthesizing isatin from o-nitrocinnamic acid. In 1883, from the o-nitrobenzaldehyde synthesis of isatin method by Bayer patent. Since then, indigo as the raw material for the synthesis of indigo gradually replace the method of extraction from plants, as the main source of indigo.

rd Merck Schuchardt OHG Germany
Product Name: Isatin
Synonyms: TIMTEC-BB SBB009100;O-AMINOPHENYLGLYOXALIC LACTIM;O-AMINOBENZOYLFORMIC ACID;O-AMINOBENZOYLFORMIC ANHYDRIDE;AKOS BBS-00003223;2,3-DIKETOINDOLINE;2,3-DIHYDROINDOLE-2,3-DIONE;2,3-INDOLEDIONE
CAS: 91-56-5
MF: C8H5NO2
MW: 147.13
EINECS: 202-077-8
mp 193-195 °C (dec.)(lit.)
Fp 220 °C
storage temp. Store at RT.
Decomposition 194 ºC
Merck 14,5104
BRN 383659
Stability: Stable. Incompatible with strong acids.

chemical property: orange-red powder or crystals

Uses
Indigo and its derivatives as indigo and related dyes and some of the raw materials for the preparation of drugs. Because of its hepatotoxicity, indigo derivatives are no longer used in the pharmaceutical industry.
A precipitant for the detection of ketones and silver. Spectrophotometric Determination of Thiophene, Thiol, Thiophene, Urine Blue and Proline.

Preparation Source
By indophenol or indigo by oxidation and prepared. Indigo was first isolated by the French chemist Auguste Laurent. In 1878, Adolf von Bayer completed the full synthesis of isatin. In 1880, Bayer developed a method of synthesizing isatin from o-nitrocinnamic acid. In 1883, from the o-nitrobenzaldehyde synthesis of isatin method by Bayer patent. Since then, indigo as the raw material for the synthesis of indigo gradually replace the method of extraction from plants, as the main source of indigo.

rd Santa Cruz Biotechnology, Inc. USA
Product Name: Isatin
Synonyms: TIMTEC-BB SBB009100;O-AMINOPHENYLGLYOXALIC LACTIM;O-AMINOBENZOYLFORMIC ACID;O-AMINOBENZOYLFORMIC ANHYDRIDE;AKOS BBS-00003223;2,3-DIKETOINDOLINE;2,3-DIHYDROINDOLE-2,3-DIONE;2,3-INDOLEDIONE
CAS: 91-56-5
MF: C8H5NO2
MW: 147.13
EINECS: 202-077-8
mp 193-195 °C (dec.)(lit.)
Fp 220 °C
storage temp. Store at RT.
Decomposition 194 ºC
Merck 14,5104
BRN 383659
Stability: Stable. Incompatible with strong acids.

chemical property: orange-red powder or crystals

Uses
Indigo and its derivatives as indigo and related dyes and some of the raw materials for the preparation of drugs. Because of its hepatotoxicity, indigo derivatives are no longer used in the pharmaceutical industry.
A precipitant for the detection of ketones and silver. Spectrophotometric Determination of Thiophene, Thiol, Thiophene, Urine Blue and Proline.

Preparation Source
By indophenol or indigo by oxidation and prepared. Indigo was first isolated by the French chemist Auguste Laurent. In 1878, Adolf von Bayer completed the full synthesis of isatin. In 1880, Bayer developed a method of synthesizing isatin from o-nitrocinnamic acid. In 1883, from the o-nitrobenzaldehyde synthesis of isatin method by Bayer patent. Since then, indigo as the raw material for the synthesis of indigo gradually replace the method of extraction from plants, as the main source of indigo.

Detailed information on the suppliers of Isatin

Properties:

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