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Sodium pentylate, also known as sodium amyloxide, is an organic compound with the chemical formula C5H11ONa. It is derived from the reaction of pentanol (an alcohol with a five-carbon chain) with sodium hydroxide, resulting in the formation of a sodium alkoxide. Sodium pentylate is a colorless liquid with a mild, alcoholic odor and is soluble in water. It is commonly used as an intermediate in the synthesis of various organic compounds, as a catalyst in certain chemical reactions, and as a component in some specialty lubricants and greases. Due to its reactivity, sodium pentylate must be handled with care, as it can react with acids and water to produce heat and potentially hazardous conditions.

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  • 1941-84-0 Structure
  • Basic information

    1. Product Name: Sodium pentylate
    2. Synonyms: Sodium pentylate
    3. CAS NO:1941-84-0
    4. Molecular Formula: C5H11O*Na
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1941-84-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Sodium pentylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Sodium pentylate(1941-84-0)
    11. EPA Substance Registry System: Sodium pentylate(1941-84-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1941-84-0(Hazardous Substances Data)

1941-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1941-84-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,4 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1941-84:
(6*1)+(5*9)+(4*4)+(3*1)+(2*8)+(1*4)=90
90 % 10 = 0
So 1941-84-0 is a valid CAS Registry Number.

1941-84-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name NaO-amylate

1.2 Other means of identification

Product number -
Other names pentan-1-ol,sodium salt

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1941-84-0 SDS

1941-84-0Upstream product

1941-84-0Relevant articles and documents

Method For Directly Producing Fine-Particle Diketopyrrolopyrrol Pigments

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Page/Page column 4, (2010/06/11)

The invention relates to a method for directly producing fine-particle 1,4-diketopyrrolo[3,4-c]pyrrols of formula (1), wherein R1a, R1b, R2a and R2b independently represent hydrogen, halogen, C1-C4 alkyl, C1-C4 alkoxy, cyano or phenyl, said compounds being characterized by a maximum frequency distribution between 20 and 120 nm. According to the method, nitriles are reacted with succinic acid esters or lactames or enamines in an alkali medium to form a pigment salt, and then protolysis of the pigment alkali salt is carried out. Said method is characterized in that an effective quantity of a pigment dispersant of formula (II) is added during the protolysis of the pigment alkali salt. In formula (II), Q is a radical of an organic pigment from the group of perinone, quinacridone, quinacridonquinone, anthanthrone, indanthrone, dioxazine, diketopyrrolopyrrol, indigo, thioindigo, thiazineindigo, isoindoline, isoindolinone, pyranthrone, isoviolanthrone, flavanthrone or anthrapyrimidine pigments.

Heterocyclic compounds their preparation and use

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, (2008/06/13)

The present invention relates to therapeutically active azacyclic or azabicyclic compounds, a method of preparing the same and to pharmaceutical compositions comprising the compounds. The novel compounds are useful as stimulants of the cognitive function of the forebrain and hippocampus of mammals and especially in the treatment of Alzheimer's disease.

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