Valproic Acid (NSC 93819) sodium salt - 10mM in DMSO , Succinate semialdehyde dehydrogenase inhibitor, CAS No.1069-66-5, Succinate semialdehyde dehydrogenase inhibitor

CAS: 1069-66-5 Cat. No.: V408675 Molecular Weight: 166.2 EC Number: 213-961-8 PubChem CID: 16760703
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GRADE & PURITY 10mM in DMSO
Synonyms
Sodium valproate | sodium 2-propylpentanoate
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Status
Price
Qty
1ml
V408675-1ml
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Information

Valproic Acid (NSC 93819) sodium salt Valproic Acid sodium salt (NSC 93819, Sodium valproate) is a HDAC inhibitor by selectively inducing proteasomal degradation of HDAC2, used in the treatment of epilepsy, bipolar disorder and prevention of migraine he
In vitro

Valproic acid acts through a distinct pathway that involves direct inhibition of histone deacetylase (IC(50) for HDAC1 = 0.4 mM). Valproic acid mimics the histone deacetylase inhibitor trichostatin A, causing hyperacetylation of histones in cultured cells. Valproic acid, like trichostatin A, also activates transcription from diverse exogenous and endogenous promoters. Valproic acid and trichostatin A have remarkably similar teratogenic effects in vertebrate embryos, while non-teratogenic analogues of valproic acid do not inhibit histone deacetylase and do not activate transcription. Valproic acid induces proliferation of peroxisomes in the rodent liver. Valproic acid at a concentration of 1 mM induces relief of this repression by Gal4 fusions of N‐CoR, TR or PPARδ in a cell line expressing the ligand‐binding domain of PPARδ fused to the DNA‐binding domain of the glucocorticoid receptor (GR) together with a GR‐controlled reporter gene. Valproic acid induces accumulation of hyperacetylated histone and inhibits HDAC activity. Valproic acid induces a specific type of differentiation characterized by reduced proliferation, morphological alterations, marker gene expression and particularly the accumulation of the AP-2 transcription factor as a potential marker of neuronal or neural crest cell-like differentiation in F9 teratocarcinoma cells. Valproic acid impairs cell proliferation or survival as indicated by decreased incorporation of [3H]thymidine in F9 and P19 teratocarcinoma cells.

In vivo

Valproic acid delays growth of the primary tumors in the MT‐450 rat breast cancer model.
Cell Data

cell lines:

Concentrations:

Incubation Time:

Powder Purity:≥98%

Specifications

Synonyms
Sodium valproate | sodium 2-propylpentanoate
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
Valproic Acid sodium salt (NSC 93819, Sodium valproate) is a HDAC inhibitor by selectively inducing proteasomal degradation of HDAC2, used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches. Valproic acid induces Notch1 si
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
INHIBITOR
Mechanism of action
Succinate semialdehyde dehydrogenase inhibitor
Names and Identifiers
Isomeric SMILES CCCC(CCC)C(=O)[O-].[Na+]
WGK Germany 3
RTECS YV7876000
PubChem CID 16760703
Molecular Weight 166.2
Reaxy-Rn 4212221

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
SolubilitySolubility (25°C) In vitro Water: 100 mg/mL warmed with 50ºC Water: bath (61.7 mM); DMSO: Insoluble; Ethanol: Insoluble;
Documents & Articles
Citations of This Product
References
1. Yuan Yuyang, Li Tianyu, Ye Zhichao, Feng Yuyao, Chen Zhe, Wang Yusen, Sun Yiqiao, Wu Haoyu, Yang Zhaodong, Wang Yifan, Zhang Yiran, Huang Liquan, Liang Bo.  (2022)  A One-Step Electropolymerized Biomimetic Polypyrrole Membrane-Based Electrochemical Sensor for Selective Detection of Valproate.  Frontiers in Bioengineering and Biotechnology,      [PMID:35242753] [10.3389/fbioe.2022.851692]
2. Guo Qing, Gan Jun, Wang En-ze, Wei Yu-ming, Xu Jie, Xu Yun, Zhang Fei-fei, Cui Meng, Jia Meng-xing, Kong Ming-jian, Tang Qiong-yao, Zhang Zhe.  (2025)  Electrophysiological characterization of human KCNT1 channel modulators and the therapeutic potential of hydroquinine and tipepidine in KCNT1 mutation-associated epilepsy mouse model.  ACTA PHARMACOLOGICA SINICA,      [PMID:39870847] [10.1038/s41401-024-01457-8]
3. Yingjun Xu, Yiming Han, Li Liu, Shanshan Han, Shibiao Zou, Bo Cheng, Fengbang Wang, Xunwei Xie, Yong Liang, Maoyong Song, Shaochen Pang.  (2024)  Highly sensitive response to the toxicity of environmental chemicals in transparent casper zebrafish.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:39032757] [10.1016/j.scitotenv.2024.174865]
4. Hongshan Li, Rongqian Mo, Jiayu Yue, Rongrong Cheng, Dianyu Li, Yusuf M. Idres, Yanmei Yang, Yanqiao Wen, Xiangrong Li, Ruofei Feng.  (2024)  Sodium valproate promotes low metabolism and high protein expression in CHO-engineered cell lines.  BIOCHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.bej.2024.109362]
5. Yuwei Zhu, Wenbo Gao, Jianlin Zheng, Ye Bai, Xinyu Tian, Tengjin Huang, Zebin Lu, De Dong, Anqi Zhang, Changyou Guo, Zhiwei Huang.  (2025)  Phosphoantigen-induced inside-out stabilization of butyrophilin receptor complexes drives dimerization-dependent γδ TCR activation.  IMMUNITY,      [PMID:40334665] [10.1016/j.immuni.2025.04.012]
6. Yang Zhao, Feiya Zhu, Jiayu Xie, Yiting Wang, Motlalepula Matsabisa, Minke Tang.  (2025)  Panax notoginseng Flower Extract Attenuates Pentylenetetrazole-Induced Epilepsy by Restoring Glutamate Homeostasis.  Brain Sciences,  15  (10): (1110).  [PMID:41154204] [10.3390/brainsci15101110]
7. Xin Gao, Xinjia Li, Yuanteng Zheng, Lijie Xia, Haonan Li, Yuqing Li, Attila Sik, Kechun Liu, Meng Jin.  (2025)  Rapid antiepileptic activity identification of isopimpinellin using a multi-model of epilepsy based on behavior-biomarker-BBB screening pipeline.  PHYTOMEDICINE,      [PMID:41351986] [10.1016/j.phymed.2025.157636]
8. Xiangxi Meng, Yumo Tian, Sen Hu, Lili Wang, Yuxian Zhong, Kui Sun, Minghua Du.  (2026)  The protective effect of sodium valproate on rats with severe scald combined with seawater immersion.  EUROPEAN JOURNAL OF MEDICAL RESEARCH,      [PMID:41709307] [10.1186/s40001-026-04043-2]
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