Welcome to chemicalbook!
China english Japan Germany India
010-86108875
18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide
Structured search
Inquriy
Try our best to find the right business for you.
Messages
Do not miss inquiry messages Please log in to view all inquiry messages.
head sculpture My chemicalbook

Welcome back!

RFQ
skype
MY Account
Top
ChemicalBook > Product Catalogue >API >Nervous system drugs >Other nervous system drugs >Pentobarbital sodium

Pentobarbital sodium

Pentobarbital sodium Structure
  • ₹0
  • Product name: Pentobarbital sodium
  • CAS: 57-33-0
  • MF: C11H17N2NaO3
  • MW: 248.25
  • EINECS:200-323-9
  • MDL Number:MFCD00070198
  • Synonyms:Pentobarbital sodium salt,5-Ethyl-5-(1-methylbutyl)-2,4,6-trioxohexahydropyrimidine, Nembutal;2,4,6(1H,3H,5H)-PyriMidinetrione,5-ethyl-5-(1-Methylbutyl)-, sodiuM salt (1:1);barpe;PENTOBARBITAL SODIUM;5-ethyl-5-(1-methylbutyl)-2,4,6(1h,3h,5h)-pyrimidinetrionemonosodiumsalt ;5-Ethyl-5-(1-Methylbutyl)-;5-ethyl-5-(1-methylbutyl)barbituricacidsodiumsalt ;5-ethyl-5-(1-methylbutyl)-barbituricacisodiumsalt
Properties Safety Information Description
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Melting point :127 °C (decomp)
solubility :H2O: soluble
form :Solid
color :Off-White
Water Solubility :Soluble to 100 mM in water
CAS DataBase Reference :57-33-0(CAS DataBase Reference)
EPA Substance Registry System :Pentobarbital sodium (57-33-0)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Danger
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H301 Toxic if swalloed Acute toxicity,oral Category 3 Danger GHS hazard pictograms P264, P270, P301+P310, P321, P330,P405, P501
Precautionary statements:
P264 Wash hands thoroughly after handling.
P264 Wash skin thouroughly after handling.
P270 Do not eat, drink or smoke when using this product.
P301+P310 IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P321 Specific treatment (see … on this label).
P330 Rinse mouth.
P405 Store locked up.
P501 Dispose of contents/container to..…

Description

Barbituric acid, the precursor of barbiturates, was first produced in 1864 by condensation of malonic acid and urea; it had no central nervous system (CNS) effects. In 1903, diethyl barbituric acid (barbital) was created as the first barbiturate with CNS inhibitory effects. Barbiturates were commonly used as sedative-hypnotics in the mid-twentieth century; meantime they were abused by some people as sold on the street. Use of barbiturates quickly dropped after introduction of benzodiazepines as the safer sedative-hypnotics. However some of the barbiturates are still used as anticonvulsants and some for euthanasia.

More related product prices

144-02-5 Ethyl cyanoacetate Sodium alginate Ethylparaben Diantimony trioxide Ethyl propiolate Ethyl acetate Sodium acetate Sodium benzoate Diclofenac sodium Etanol Sodium hydroxide Trinexapac-ethyl Ethyl acrylate Sodium bicarbonate Sodium citrate Aluminum oxide Trisodium phosphate

Related product price