INACTIN

INACTIN Structure
CAS No.
947-08-0
Chemical Name:
INACTIN
Synonyms
inaktin;INACTIN;narkothion;brevinarcon;brevinarcone;venobarbital;Inactin? hydrate;Thiobutabarbital;thiobutabarbitonesodium;THIOBUTABARBITAL SODIUM
CBNumber:
CB6486701
Molecular Formula:
C10H15N2NaO2S
Molecular Weight:
250.29
MOL File:
947-08-0.mol
Modify Date:
2024/3/19 15:37:50

INACTIN Properties

Melting point 167-168 °C
solubility H2O: storage of solutions for more than 8 hours at 4°C is not recommended.soluble
form solid
color light yellow
PH pH:9.0~11.0 (50g/l, 25℃)
EPA Substance Registry System Thiobutabarbital sodium (947-08-0)

SAFETY

Risk and Safety Statements

WGK Germany  3
RTECS  CQ2278000

INACTIN Chemical Properties,Uses,Production

Uses

Inactin? hydrate has been used to anesthetize rats to study stress-induced hypersensitivity and mice to study Cisplatin-induced neuropathy. It has also been used to anesthetize rats to measure the glomerular filtration rate (GFR).

General Description

Crystals.

Air & Water Reactions

Slight hygroscopic. Water soluble.

Reactivity Profile

An amine, organosulfide. Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.

Fire Hazard

Flash point data for INACTIN are not available. INACTIN is probably combustible.

INACTIN Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 12)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 China 9708 58 Inquiry
Wako Pure Chemical Industries, Ltd. +81 6 6203 3741 Japan 6828 80 Inquiry
SIGMA-RBI 800 736 3690 (Orders) Switzerland 6913 91 Inquiry
Service Chemical Inc. 888-895-6920 Germany 6373 71 Inquiry
3B Scientific Corporation 847.281.9822 United States 6744 47 Inquiry
HONEST JOY HOLDINGS LIMITED +86-755-26404303 United States 6702 54 Inquiry
Lanospharma Laboratories Co.,Ltd 13440048448 China 6343 56 Inquiry
Riedel-de Haen AG 800 558-9160 United States 6825 87 Inquiry
Shanghai Xiyuan Biotechnology Co., Ltd 021-58116080 CHINA 6936 58 Inquiry
5-sec-butyl-5-ethyl-2-thiobarbituricacidsodiumsalt 5-sec-butyl-5-ethyl-2-thio-barbituricacisodiumsalt 6(1h,5h)-pyrimidinedione,5-ethyldihydro-5-(1-methylpropyl)-2-thioxo-mono 5-Ethyl-5-[1-methylpropyl]-2-thiobarbituric acid, sodium salt 4,6(1H,5H)-PyriMidinedione, 5-ethyldihydro-5-(1-Methylpropyl)-2-thioxo-, sodiuM salt Inactin? hydrate Thiobutabarbital sodium salt hydrate brevinarcon brevinarcone inaktin narkothion thiobutabarbitonesodium venobarbital INACTIN THIOBUTABARBITAL SODIUM THIOBUTABARBITAL SODIUM SALT 5-(sec-butyl)-5-ethyldihydro-2-thioxopyrimidine-4,6(1H,5H)-dione, monosodium salt Thiobutabarbital 5-butan-2-yl-5-ethyl-2-sulfanylidenepyrimidin-3-ide-4,6-dione 947-08-0 C10H15N2NaO2S C10H15N2O2SNa