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Hydroxylated lecithin

HCID 97663
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
1955-68-6
Standard SMILES
N[C@@H](CC(=O)NO)C(=O)O
InChIKey
ZBYVTTSIVDYQSO-REOHCLBHSA-N
Molecular formula
C4H8N2O4
Average molar mass
148.12 g/mol
Monoisotopic mass
148.04840674

Overview

Beta-L-aspartylhydroxamic acid is a non-proteinogenic L-alpha-amino acid that is L-asparagine hydroxylated at N-4. It is a hydroxamic acid, a L-asparagine derivative and a non-proteinogenic L-alpha-amino acid. It is a tautomer of a beta-L-aspartylhydroxamic acid zwitterion.

Names & identifiers

Preferred name
Hydroxylated lecithin
IUPAC
(2S)-2-amino-4-(hydroxyamino)-4-oxobutanoic acid
English name
L-Aspartic acid beta-hydroxamate
Molecular formula
C4H8N2O4
Molecular weight
148.12

Names & synonyms

(2S)-2-amino-3-(hydroxycarbamoyl)propanoic acidLecithin, hydroxylatedRefChem:789520DTXSID1093751EINECS 232-440-6L-Aspartic acid beta-hydroxamate1955-68-6N-Hydroxy-L-asparagineN4-Hydroxy-L-asparagine(2S)-2-amino-4-(hydroxyamino)-4-oxobutanoic acidbeta-L-AspartylhydroxamateL-Aspartic acid |A-hydroxamate
Show more names
AAHl-aspartic acid β-hydroxamateHDXNsc141662L-β-Aspartohydroxamic acidL-ASPARTICACIDβ-HYDROXAMATEL-Aspartyl-?-hydroxamic acid3-(Hydroxycarbamoyl)-L-alanine
beta-L-aspartylhydroxamic acidbeta-aspartohydroxamic acidCHEMBL63902L-Asparaginsaeure-4-hydroxyamidL-Asparagine, N-hydroxy-D-Aspartic acid beta-hydroxamateLecithin ethoxylatedSD4

Database identifiers

CAS
1955-68-6、8029-76-3

Properties

Computed structural properties

XLogP
-3.5
Topological polar surface area
113 Ų
Hydrogen bond donors
4
Hydrogen bond acceptors
5
Rotatable bonds
3
Heavy atoms
10
Formal charge
0
Complexity
146

Physicochemical properties

Melting point
171 · 171-172 °C
Density
1.532 · 1.532±0.06 g/cm3(Predicted)
storage temp.
20 °C · −20°C
pka
3.02 · 3.02±0.10(Predicted)
form
Solid
color
White to off-white
Major Application
detection
InChI
1S/C4H8N2O4/c5-2(4(8)9)1-3(7)6-10/h2,10H,1,5H2,(H,6,7)(H,8,9)/t2-/m0/s1
InChIKey
ZBYVTTSIVDYQSO-REOHCLBHSA-N
SMILES
N[C@@H](CC(=O)NO)C(O)=O
UNSPSC Code
12352209 · 12352209
NACRES
26 · NA.26
PPE
95 · Eyeshields, Gloves, type N95 (US)
WGK Germany
3 · 3
Storage Class
11 · 11 - Combustible Solids

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Safety data

PPE
Eyeshields, Gloves, type N95 (US)
wgk
3
Storage Class
11 - Combustible Solids

Chemistry & industry

Pharmacology

Cellular LocationsCytoplasm

Uses & manufacturing

Use ClassificationFood Additives -> EMULSIFIER -> JECFA Functional Classes
Applications · 2 items

DescriptionHydroxylated lecithin, also known as b-L-aspartylhydroxamate or b-aspartohydroxamic acid, belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. Based on a literature review a small amount of articles have been published on Hydroxylated lecithin.

UsesL-ASPARTIC ACID BETA-HYDROXAMATE can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical and pharmaceutical production process.

Suppliers21 total

上海麦克林生化科技股份有限公司021-50706066 15221275939 · [email protected]
河北展药生物科技有限公司15369953316 +8615369953316 · [email protected]
Aladdin Scientific[email protected]
Syntechem Co.,Ltd[email protected]
广东元丰化学试剂有限公司0751-2829979 13318593351 · [email protected]
Hebei Shengyuan Jinlong Import and Export Co. LTD

Related reactions

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
PubChem CID
97663
ChEMBL
CHEMBL63902
ChEBI
CHEBI:52794
Nikkaji
J372.799H
+86-17367750398 · [email protected]
广州爱纯医药科技有限公司020-39119399 18927568969 · [email protected]
邯郸统溢新材料科技有限公司17330042575 · [email protected]
广东翁江化学试剂有限公司0751-2815987 13927875076 · [email protected]
安耐吉化学&3A(安徽泽升科技股份有限公司)400-0056266 · [email protected]
Qiuxian Baitai New Material Co., LTD+86-19932103556 · [email protected]
陕西缔都医药化工有限公司+86-29-81139210 +86-17392587031 · [email protected]
上海吉奉生物科技有限公司021-61263377 15023907684 · [email protected]
江苏洪珉药业有限公司18221292452 · [email protected]
陕西缔都医药有限责任公司81148925 17391631969 · [email protected]
BOC Sciences+1-631-485-4226 · [email protected]
上海皓鸿生物医药科技有限公司400-8210725 4008210725 · [email protected]
DAYANG CHEM (HANGZHOU) CO.,LTD+86-88938639 +86-17705817739 · [email protected]
江苏艾康生物医药研发有限公司025-58859352 18651614124 · [email protected]
Henan Lavoisier Chemical Products Co.Ltd+86-86-37163682289 +8615981966935 · [email protected]
Dideu Industries Group Limited+86-29-81148696 +86-15129568250 · [email protected]
Additional notes · 1 item

DefinitionChEBI: Beta-L-aspartylhydroxamic acid is a non-proteinogenic L-alpha-amino acid that is L-asparagine hydroxylated at N-4. It is a hydroxamic acid, a L-asparagine derivative and a non-proteinogenic L-alpha-amino acid. It is a tautomer of a beta-L-aspartylhydroxamic acid zwitterion.