H-Aib-OMe.HCl

Modify Date: 2024-01-02 12:12:40

H-Aib-OMe.HCl Structure
H-Aib-OMe.HCl structure
Common Name H-Aib-OMe.HCl
CAS Number 15028-41-8 Molecular Weight 153.61
Density N/A Boiling Point 120.6ºC at 760mmHg
Molecular Formula C5H12ClNO2 Melting Point 185°C
MSDS Chinese USA Flash Point 56.1ºC

 Use of H-Aib-OMe.HCl


Methyl 2-aminoisobutyrate hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name Alpha-Aminoisobutyric Acid Methyl Ester Hydrochloride
Synonym More Synonyms

 H-Aib-OMe.HCl Biological Activity

Description Methyl 2-aminoisobutyrate hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog

 Chemical & Physical Properties

Boiling Point 120.6ºC at 760mmHg
Melting Point 185°C
Molecular Formula C5H12ClNO2
Molecular Weight 153.61
Flash Point 56.1ºC
Exact Mass 153.055649
PSA 52.32000
LogP 1.39900
Vapour Pressure 15.1mmHg at 25°C
Storage condition −20°C

 MSDS

Material Safety Data Sheet

Section1. Identification of the substance
Product Name: Alpha-aminoisobutyric acid methyl ester, HCl
Synonyms:Methyl 2-aminoisobutyrate HCl

Section2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

Section3. Composition/information on ingredients.
Ingredient name:Alpha-aminoisobutyric acid methyl ester, HCl
CAS number:15028-41-8

Section4. First aid measures
Skin contact:Immediately wash skin with copious amounts of water for at least 15 minutes while removing
contaminated clothing and shoes. If irritation persists, seek medical attention.
Eye contact:Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
flushing of the eyes by separating the eyelids with fingers. If irritation persists, seek medical
attention.
Inhalation:Remove to fresh air. In severe cases or if symptoms persist, seek medical attention.
Ingestion:Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.

Section5. Fire fighting measures
In the event of a fire involving this material, alone or in combination with other materials, use dry
powder or carbon dioxide extinguishers. Protective clothing and self-contained breathing apparatus
should be worn.

Section6. Accidental release measures
Personal precautions: Wear suitable personal protective equipment which performs satisfactorily and meets local/state/national
standards.
Respiratory precaution:Wear approved mask/respirator
Hand precaution:Wear suitable gloves/gauntlets
Skin protection:Wear suitable protective clothing
Eye protection:Wear suitable eye protection
Methods for cleaning up: Mix with sand or similar inert absorbent material, sweep up and keep in a tightly closed container
for disposal. See section 12.
Environmental precautions: Do not allow material to enter drains or water courses.

Section7. Handling and storage
Handling:This product should be handled only by, or under the close supervision of, those properly qualified
in the handling and use of potentially hazardous chemicals, who should take into account the fire,
health and chemical hazard data given on this sheet.
Store in closed vessels.
Storage:

Section8. Exposure Controls / Personal protection
Engineering Controls: Use only in a chemical fume hood.
Personal protective equipment: Wear laboratory clothing, chemical-resistant gloves and safety goggles.
General hydiene measures: Wash thoroughly after handling. Wash contaminated clothing before reuse.

Section9. Physical and chemical properties
Appearance:Not specified
Boiling point:No data
No data
Melting point:
Flash point:No data
Density:No data
Molecular formula:C5H11NO2.ClH
Molecular weight:153.6

Section10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, nitrogen oxides, hydrogen chloride.

Section11. Toxicological information
No data.

Section12. Ecological information
No data.

Section13. Disposal consideration
Arrange disposal as special waste, by licensed disposal company, in consultation with local waste
disposal authority, in accordance with national and regional regulations.

Section14. Transportation information
Non-harzardous for air and ground transportation.

Section15. Regulatory information
No chemicals in this material are subject to the reporting requirements of SARA Title III, Section
302, or have known CAS numbers that exceed the threshold reporting levels established by SARA
Title III, Section 313.


SECTION 16 - ADDITIONAL INFORMATION
N/A

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2922499990

 Customs

HS Code 2922499990
Summary HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0%

 Articles4

More Articles
An efficient and expedient method for the synthesis of 11C-labeled α-aminoisobutyric acid: a tumor imaging agent potentially useful for cancer diagnosis.

Bioorg. Med. Chem. Lett. 21 , 2437-2440, (2011)

We describe the synthesis of (11)C-labeled α-aminoisobutyric acid 2 from iodo[(11)C]methane and methyl N-(diphenylmethylen)-d,l-alaniate (5). The tetrabutylammonium fluoride (TBAF)-promoted α-[(11)C]m...

Peptide sweeteners. 6. Structural studies on the C-terminal amino acid of L-aspartyl dipeptide sweeteners.

J. Med. Chem. 27 , 1663-1668, (1984)

Stereochemical and structural aspects of the variations in the C-terminal residue of L-aspartyl-L-phenylalanine methyl ester have been investigated. Novel configurational analogues such as L-aspartyl-...

Characterization of glycine transport in cultured Müller glial cells from the retina.

Glia 26 , 273-279, (1999)

Rapid termination of the synaptic action of glutamate (Glu) and glycine (Gly) is achieved by uptake into the presynaptic terminal and glial cells. In the vertebrate CNS, Gly acts both as an inhibitory...

 Synonyms

2-Aminoisobutyric acid methyl ester hydrochloride
Methyl 2-Aminoisobutyrate Hydrochloride
MFCD00214247
methyl 2-amino-2-methylpropanoate,hydrochloride
Methyl 2-amino-2-methylpropanoate hydrochloride
Methyl α-aminoisobutyrate hydrochloride
Methyl alpha-aminoisobutyrate hydrochloride
α-Aminoisobutyric acid methyl ester hydrochloride
Alanine, 2-methyl-, methyl ester, hydrochloride (1:1)
Methyl 2-methylalaninate hydrochloride (1:1)
H-Aib-OMe.HCl
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