INDOLE-3-ACETALDEHYDE SODIUM BISULFITE ADDITION COMPOUND

Product Name: INDOLE-3-ACETALDEHYDE SODIUM BISULFITE ADDITION COMPOUND
CAS No.: 20095-27-6
Chemical Name: INDOLE-3-ACETALDEHYDE SODIUM BISULFITE ADDITION COMPOUND
Synonyms: Tryptophan Impurity 111;indole-3-acetaldehyde sodium bisulfite;INDOLE-3-ACETALDEHYDE SODIUM BISULFATE);3-INDOLE-3-ACETALDEHYDE SODIUM BISULFITE;3-INDOLEACETALDEHYDE BISULFITE ADDITION COMPOUND;2'-O-MONOBUTYRYLGUANOSINE 3':5'-CYCLIC*M ONOPHOSPHAT;Sodium 1-Hydroxy-2-(1H-indol-3-yl)ethane-1-sulfonate;INDOLE-3-ACETALDEHYDE SODIUM BISULFITE ADDITION COMPOUND;1H-Indole-3-ethanesulfonic acid, α-hydroxy-, sodium salt (1:1)
CBNumber: CB5130351
Molecular Formula: C10H10NO4S.Na
Formula Weight: 263.25
MOL File: 20095-27-6.mol

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INDOLE-3-ACETALDEHYDE SODIUM BISULFITE ADDITION COMPOUND Property

storage temp.: 2-8°C

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Safety

Hazard Codes: Xi
Risk Statements: 36/37/38
Safety Statements: 26-36
WGK Germany: 3

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: I1000
Product name: Indole-3-acetaldehyde–sodium bisulfite addition compound
Packaging: 25mg
Price: $75.1
Updated: 2024/03/01

Sigma-Aldrich

Product number: I1000
Product name: Indole-3-acetaldehyde–sodium bisulfite addition compound
Packaging: 100mg
Price: $245
Updated: 2024/03/01

American Custom Chemicals Corporation

Product number: CHM0237516
Product name: 3-INDOLE-3-ACETALDEHYDE SODIUM BISULFITE
Purity: 98.00%
Packaging: 1G
Price: $1270.5
Updated: 2021/12/16

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INDOLE-3-ACETALDEHYDE SODIUM BISULFITE ADDITION COMPOUND Chemical Properties,Usage,Production

Uses

• ;Reactant for preparation of potential neurotransmitter analogs1• ;Reactant for Strecker reaction with cyanide-11C2

Uses

Reactant for preparation of potential neurotransmitter analogs
Reactant for Strecker reaction with cyanide-11C

INDOLE-3-ACETALDEHYDE SODIUM BISULFITE ADDITION COMPOUND Preparation Products And Raw materials

Raw materials

Preparation Products

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INDOLE-3-ACETALDEHYDE SODIUM BISULFITE ADDITION COMPOUND Suppliers

China 12 Germany 1 Switzerland 1 United Kingdom 1 United States 4 Global 19

RYSS TECH LTD

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Sigma-Aldrich

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Hubei Yangxin Medical Technology Co., Ltd.

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Aikon International Limited

Tel: 025-66113011 18112977050
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Hefei TNJ Chemical Industry Co.,Ltd.

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Energy Chemical

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Shanghai Haohong Scientific Co., Ltd.

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Hubei Qingbei Yunyan Pharmaceutical Technology Co., Ltd

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Jilin Chinese Academy of Sciences-yanshen Technology

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20095-27-6, INDOLE-3-ACETALDEHYDE SODIUM BISULFITE ADDITION COMPOUNDRelated Search:

Sodium bisulfite ETHANESULFONIC ACID SODIUM SALT Sodium hydroxymethanesulphinate ETHANESULFONIC ACID SODIUM SALT MONO- INDOLE-3-ACETALDEHYDE SODIUM BISULFITE ADDITION COMPOUND Sodium ethanesulfinate Tryptophol Formaldehyde sodium bisulfite Sodium 1-propanesulfonate ACETALDEHYDE SODIUM BISULFITE

3-INDOLE-3-ACETALDEHYDE SODIUM BISULFITE

3-INDOLEACETALDEHYDE BISULFITE ADDITION COMPOUND

INDOLE-3-ACETALDEHYDE SODIUM BISULFITE ADDITION COMPOUND

indole-3-acetaldehyde sodium bisulfite

2'-O-MONOBUTYRYLGUANOSINE 3':5'-CYCLIC*M ONOPHOSPHAT

INDOLE-3-ACETALDEHYDE SODIUM BISULFATE)

1H-Indole-3-ethanesulfonic acid, α-hydroxy-, sodium salt (1:1)

Sodium 1-Hydroxy-2-(1H-indol-3-yl)ethane-1-sulfonate

Tryptophan Impurity 111

20095-27-6

C10H11NNaO4S

C10H9NOHNaO3S

C10H9NONaHSO3

C10H10NNaO4S

Heterocyclic Building Blocks

Indoles

Building Blocks

Heterocyclic Building Blocks

Building Blocks

C10

Chemical Synthesis

Heterocyclic Building Blocks

Indoles

Heterocyclic Compounds