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INACTIN

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
MDL Number:
MFCD00214068
MOL File:
947-08-0.mol
Last updated:2024-03-19 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℃)
FDA UNII VE5XWZ299Q
EPA Substance Registry System Thiobutabarbital sodium (947-08-0)

SAFETY

Risk and Safety Statements

WGK Germany  3
RTECS  CQ2278000

INACTIN price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich T133 Inactin? hydrate ≥98% (HPLC) 947-08-0 1g $126 2024-03-01 Buy
Sigma-Aldrich T133 Inactin? hydrate ≥98% (HPLC) 947-08-0 5x1g $453 2024-03-01 Buy
Sigma-Aldrich T133 Inactin? hydrate ≥98% (HPLC) 947-08-0 25x1g $1630 2024-03-01 Buy
American Custom Chemicals Corporation API0004392 THIOBUTABARBITAL SODIUM SALT 95.00% 947-08-0 100MG $1695.03 2021-12-16 Buy
Product number Packaging Price Buy
T133 1g $126 Buy
T133 5x1g $453 Buy
T133 25x1g $1630 Buy
API0004392 100MG $1695.03 Buy

INACTIN Chemical Properties,Uses,Production

Description

Thiobutabarbital sodium , the sodium salt of 5-sec-butyl-5-ethylthiobarbituric acid, is a yellowishwhite amorphous powder soluble in water and alcohol. The colorless crystals of the free acid melt at 163 – 165 ?C. Thiobutabarbital is prepared from thiourea and a malonic ester .

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.

Biochem/physiol Actions

Inactin? is a long-lasting rodent anesthetic with minimal effects on cardiovascular tone and renal output. It exhibits sedative and hypnotic properties.

Clinical Use

It is a short-acting intravenous anesthetic. It is the least potent of the thiobarbiturates and therefore causes the least number of complications during anesthesia. The compound is available as 5 % and 10 % solutions.

INACTIN Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 12)Suppliers
Supplier Tel Email Country ProdList Advantage
Shanghai ZaiQi Bio-Tech Co., Ltd. 021-54824098, 021-37212705 021-37212706, 13391256916 sales@chemzq.com China 570 55
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9806 58
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