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45945

Supelco

Isopropylamine

anhydrous, analytical standard

Synonyme(s) :

2-Aminopropane

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About This Item

Formule linéaire :
(CH3)2CHNH2
Numéro CAS:
75-31-0
Poids moléculaire :
59.11
Numéro Beilstein :
605259
Numéro CE :
200-860-9
Numéro MDL:
MFCD00008082
Code UNSPSC :
41116107
ID de substance PubChem :
329757019
Nomenclature NACRES :
NA.24

Qualité

analytical standard
anhydrous

Densité de vapeur

2.04 (vs air)

Pression de vapeur

9.2 psi ( 20 °C)

Température d'inflammation spontanée

755 °F

Durée de conservation

limited shelf life, expiry date on the label

Limite d'explosivité

10.4 %

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.374 (lit.)

Point d'ébullition

33-34 °C (lit.)

Densité

0.688 g/mL at 20 °C (lit.)

Application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

CC(C)N

InChI

1S/C3H9N/c1-3(2)4/h3H,4H2,1-2H3

Clé InChI

JJWLVOIRVHMVIS-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictogrammes

FlameSkull and crossbonesCorrosion
GHS02,GHS06,GHS05

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 1 - Skin Corr. 1A - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

<-13.0 °F - closed cup

Point d'éclair (°C)

<= -25 °C - closed cup

Équipement de protection individuelle

Faceshields, Gloves, Goggles

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Certificats d'analyse (COA)

Lot/Batch Number
BCCM0005
BCCL2209
BCCK4254
BCCH6119
BCCF5389

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Donna L McGovern et al.
Journal of molecular graphics & modelling, 28(7), 612-625 (2010-01-20)
The highly potent and kappa-opioid (KOP) receptor-selective hallucinogen Salvinorin A and selected analogs have been analyzed using the 3D quantitative structure-affinity relationship technique Comparative Molecular Field Analysis (CoMFA) in an effort to derive a statistically significant and predictive model of
Omar Deeb et al.
Chemical biology & drug design, 71(4), 352-362 (2008-03-04)
The aim of this study is to provide an initial indication regarding the scope and limitations of some state-of-the-art methods in computational chemistry, including semiempirical (AM1) and density functional theory (B3LYP), in the flip regression procedure applied to the inhibition
Jacek Lipok et al.
Ecotoxicology and environmental safety, 73(7), 1681-1688 (2010-09-04)
The toxicity of commercial formulation of Roundup® 360 SL, widely used, nonselective herbicide and its main constituents, glyphosate (PMG), equimolar (1:1) isopropylamine salt of glyphosate (GIPA) and isopropylamine (IPA) was examined towards eight aquatic microphotoautotrophs; seven cyanobacterial strains representing either
Bambang Veriansyah et al.
Journal of hazardous materials, 124(1-3), 119-124 (2005-06-09)
Supercritical water oxidation can effectively destroy a large variety of high-risk wastes resulting from munitions demilitarization and complex industrial chemical. An important design consideration in the development of supercritical water oxidation is the information on the oxidation rate. In this
Katrijn De Klerck et al.
Journal of chromatography. A, 1234, 72-79 (2011-12-07)
In chiral supercritical fluid chromatography (SFC), mobile-phase additives are often used to improve enantioseparations and peak shapes. An acidic or basic additive is chosen, depending on the nature of the compound. This work highlights the simultaneous use of the acidic
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