N-(2-methyl-1-oxobutyl)-Glycine

Modify Date: 2024-01-09 11:34:29

N-(2-methyl-1-oxobutyl)-Glycine Structure
N-(2-methyl-1-oxobutyl)-Glycine structure
Common Name N-(2-methyl-1-oxobutyl)-Glycine
CAS Number 52320-67-9 Molecular Weight 159.18300
Density 1.097g/cm3 Boiling Point 371.8ºC at 760mmHg
Molecular Formula C7H13NO3 Melting Point N/A
MSDS N/A Flash Point 178.7ºC

 Use of N-(2-methyl-1-oxobutyl)-Glycine


N-(2-Methylbutyryl)glycine is a Glycine (HY-Y0966) derivative[1].

 Names

Name N-(2-methylbutanoyl)glycine
Synonym More Synonyms

 N-(2-methyl-1-oxobutyl)-Glycine Biological Activity

Description N-(2-Methylbutyryl)glycine is a Glycine (HY-Y0966) derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

 Chemical & Physical Properties

Density 1.097g/cm3
Boiling Point 371.8ºC at 760mmHg
Molecular Formula C7H13NO3
Molecular Weight 159.18300
Flash Point 178.7ºC
Exact Mass 159.09000
PSA 69.89000
LogP 1.07360
Index of Refraction 1.458

 Safety Information

HS Code 2924199090

 Synthetic Route

~%

N-(2-methyl-1-oxobutyl)-Glycine Structure

N-(2-methyl-1-o...

CAS#:52320-67-9

Literature: Gregersen; Keiding; Kolvraa Biomedical Mass Spectrometry, 1979 , vol. 6, # 10 p. 439 - 443

 Precursor & DownStream

Precursor  2

DownStream  0

 Customs

HS Code 2924199090
Summary 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Synonyms

N-(2-Methylbutyryl)glycine
N-sec.-Valerylglycin
N-sec-Valerylglycine
2-(2-methylbutanoylamino)acetic acid
2-(2-methylbutanamido)acetic acid
2-methylbutyrylglycine
a-methylbutyrylglycine
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