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4-Methyl-2-oxovaleric acid - 90%, high purity , CAS No.816-66-0

2 Citations

Moligand™

≥90%

CAS#: 816-66-0
Formula: C₆H₁₀O₃
Molecular Weight: 130.14
Beilstein Registry Number: 1701823
EC Number: 212-435-5
MDL number: MFCD00066204
PubChem CID: 70

Item Number

M401024

Grouped product items
SKU	Size	Availability	Price	Qty
M401024-25g	25g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$559.90
M401024-100g	100g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$1,957.90

Basic Description

Synonyms	2-keto-4-methyl-pentanoate \| 2-oxo-4-methylpentanoate \| 2-Oxo-4-methylvaleric acid \| NCGC00246997-01 \| D82408 \| Isopropylpyruvic acid \| STR07443 \| HY-W012722 \| UNII-4GUJ8AH400 \| a-Ketoisocapronate \| 2-Keto-4-methylpentanoic acid \| 4-Methyl-2-oxovaleric ac
Specifications & Purity	Moligand™, ≥90%
Storage Temp	Store at 2-8°C
Shipped In	Wet ice
Grade	Moligand™
Product Description	An intermediate in the metabolism of leucine.

Associated Targets(Human)

SLC16A7 Tchem Monocarboxylate transporter 2 (0 Activities)

Discover Target: SLC16A7

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC16A3 Tchem Monocarboxylate transporter 4 (0 Activities)

Discover Target: SLC16A3

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC16A1 Tchem Monocarboxylate transporter 1 (0 Activities)

Discover Target: SLC16A1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)

Discover Target: SLC16A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC16A3 Tchem Monocarboxylate transporter 4 (196 Activities)

Discover Target: SLC16A3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Names and Identifiers

IUPAC Name	4-methyl-2-oxopentanoic acid
INCHI	InChI=1S/C6H10O3/c1-4(2)3-5(7)6(8)9/h4H,3H2,1-2H3,(H,8,9)
InChi Key	BKAJNAXTPSGJCU-UHFFFAOYSA-N
Canonical SMILES	CC(C)CC(=O)C(=O)O
Isomeric SMILES	CC(C)CC(=O)C(=O)O
WGK Germany	3
PubChem CID	70
UN Number	3265
Molecular Weight	130.14
Beilstein	1701823
Reaxy-Rn	1701823

Refractive Index

1.431

Flash Point(°C)

83 °C

Boil Point(°C)

85 °C

Melt Point(°C)

8-10°C

Safety and Hazards(GHS)

Pictogram(s)	GHS05
Signal	Danger
Hazard Statements	H314:Causes severe skin burns and eye damage
Precautionary Statements	P280:Wear protective gloves/protective clothing/eye protection/face protection. P321:Specific treatment (see ... on this label). P405:Store locked up. P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P260:Do not breathe dust/fume/gas/mist/vapors/spray. P301+P330+P331:IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing. P363:Wash contaminated clothing before reuse. P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing. P302+P361+P354:IF ON SKIN: Take off Immediately all contaminated clothing. Immediately rinse with water for several minutes. P316:Get emergency medical help immediately.
WGK Germany	3
Reaxy-Rn	1701823

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Xinjian Yin, Yayun Liu, Lijun Meng, Haisheng Zhou, Jianping Wu, Lirong Yang. (2020) Semi-rational hinge engineering: modulating the conformational transformation of glutamate dehydrogenase for enhanced reductive amination activity towards non-natural substrates. Catalysis Science & Technology, 10 (10): (3376-3386). [PMID:] [10.1039/C9CY02576F]
2. Xinjian Yin, Yayun Liu, Lijun Meng, Haisheng Zhou, Jianping Wu, Lirong Yang. (2018) Rational Molecular Engineering of Glutamate Dehydrogenases for Enhancing Asymmetric Reductive Amination of Bulky α-Keto Acids. ADVANCED SYNTHESIS & CATALYSIS, 361 (4): (803-812). [PMID:] [10.1002/adsc.201801251]

References

1. Xinjian Yin, Yayun Liu, Lijun Meng, Haisheng Zhou, Jianping Wu, Lirong Yang. (2020) Semi-rational hinge engineering: modulating the conformational transformation of glutamate dehydrogenase for enhanced reductive amination activity towards non-natural substrates. Catalysis Science & Technology, 10 (10): (3376-3386). [PMID:] [10.1039/C9CY02576F]
2. Xinjian Yin, Yayun Liu, Lijun Meng, Haisheng Zhou, Jianping Wu, Lirong Yang. (2018) Rational Molecular Engineering of Glutamate Dehydrogenases for Enhancing Asymmetric Reductive Amination of Bulky α-Keto Acids. ADVANCED SYNTHESIS & CATALYSIS, 361 (4): (803-812). [PMID:] [10.1002/adsc.201801251]

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4-Methyl-2-oxovaleric acid - 90%, high purity , CAS No.816-66-0

Basic Description

Associated Targets(Human)

Associated Targets(non-human)

Mechanisms of Action

Names and Identifiers

Certificates

Certificate of Analysis(COA)

Chemical and Physical Properties