laevo-norleucine, 327-57-1

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CODE125389 CODE125389
Product(s):
327-57-1 L-Norleucine 95%
A non-essential amino acid. Used as internal standard in amino acid analysis.

Glentham Life Sciences Ltd

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CODE125389 CODE125389
Product(s):
GM2610 L-norLeucine

TCI AMERICA

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CODE125389 CODE125389
Product(s):
N0303 L-norLeucine >99.0%(T)
SDS

CAS Number:	327-57-1	3D/inchi
Other(deleted CASRN):	1013313-52-4
ECHA EINECS - REACH Pre-Reg:	206-321-4
FDA UNII:	832C8OV84S
Nikkaji Web:	J9.189H
Beilstein Number:	1721750
MDL:	MFCD00064423
XlogP3:	-1.50 (est)
Molecular Weight:	131.17501000
Formula:	C6 H13 N O2
BioActivity Summary:	listing
NMR Predictor:	Predict (works with chrome, Edge or firefox)

Category:natural substances and extractives

US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:

Google Scholar:	Search
Google Books:	Search
Google Scholar: with word "volatile"	Search
Google Scholar: with word "flavor"	Search
Google Scholar: with word "odor"	Search
Google Patents:	Search
US Patents:	Search
EU Patents:	Search
Pubchem Patents:	Search
PubMed:	Search
NCBI:	Search

Physical Properties:

Assay:	95.00 to 100.00
Food Chemicals Codex Listed:	No
Boiling Point:	234.00 °C. @ 760.00 mm Hg (est)
Flash Point:	204.00 °F. TCC ( 95.30 °C. ) (est)
logP (o/w):	0.920 (est)
Soluble in:
	water, 1.20E+04 mg/L @ 25 °C (exp)
	water, 1.569e+004 mg/L @ 25 °C (est)

Organoleptic Properties:

Odor and/or flavor descriptions from others (if found).

Cosmetic Information:

None found

Suppliers:

BOC Sciences

For experimental / research use only.

L-Norleucine 95%

Odor: characteristic

Use: A non-essential amino acid. Used as internal standard in amino acid analysis.

Changzhou Longo Chemical

L-norLeucine

ExtraSynthese

For experimental / research use only.

L-(+)-norLeucine

Glentham Life Sciences

L-norLeucine

Santa Cruz Biotechnology

For experimental / research use only.

L-(+)-norLeucine ≥99%

Sigma-Aldrich: Sigma

For experimental / research use only.

L-norLeucine ≥98% (TLC)

sds

TCI AMERICA

For experimental / research use only.

L-norLeucine >99.0%(T)

sds

Safety Information:

Preferred SDS: View

Hazards identification

Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements

Pictogram

Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in Use Information:

Category:
natural substances and extractives
Recommendation for laevo-norleucine usage levels up to:
	not for fragrance use.

Recommendation for laevo-norleucine flavor usage levels up to:
	not for flavor use.

Safety References:

EPI System: View

ClinicalTrials.gov:search

AIDS Citations:Search

Cancer Citations:Search

Toxicology Citations:Search

EPA Substance Registry Services (TSCA):327-57-1

EPA ACToR:Toxicology Data

EPA Substance Registry Services (SRS):Registry

Laboratory Chemical Safety Summary :21236

National Institute of Allergy and Infectious Diseases:Data

WGK Germany:3

(2S)-2-aminohexanoic acid

Chemidplus:0000327571

RTECS:RC6308000 for cas# 327-57-1

References:

	(2S)-2-aminohexanoic acid
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	21236
Pubchem (sid):	134973448

Other Information:

(IUPAC):	Atomic Weights of the Elements 2011 (pdf)
Videos:	The Periodic Table of Videos
tgsc:	Atomic Weights use for this web site
(IUPAC):	Periodic Table of the Elements
CHEBI:	View
CHEMBL:	View
Golm Metabolome Database:	Search
Metabolomics Database:	Search
KEGG (GenomeNet):	C01933
HMDB (The Human Metabolome Database):	HMDB01645
FooDB:	FDB022699
YMDB (Yeast Metabolome Database):	YMDB01001
Export Tariff Code:	2922.49.4050
ChemSpider:	View

Potential Blenders and core components note

None Found

Potential Uses:

None Found

Occurrence (nature, food, other):note

not found in nature

Synonyms:

(2S)-2-	aminohexanoic acid
(S)-2-	aminohexanoic acid
	hexanoic acid, 2-amino-, (S)-
L-(+)-nor	leucine
L-nor	leucine

Articles:

PubMed:Gas chromatographic quantification of free D-amino acids in higher vertebrates.

PubMed:Pyridinium-carbaldehyde: active Maillard reaction product from the reaction of hexoses with lysine residues.

PubMed:Spiro cross-links: representatives of a new class of glycoxidation products.

PubMed:Identification of new heterocyclic nitrogen compounds from glucose-lysine and xylose-lysine maillard model systems.

PubMed:Olfactory discrimination of amino acids in brown bullhead catfish.

Notes:

An unnatural amino acid that is used experimentally to study protein structure and function. It is structurally similar to methionine, however it does not contain sulfur. Aminocaproic acid works as an antifibrinolytic. It is a derivative of the amino acid lysine. It binds reversibly to the kringle domain of plasminogen and blocks the binding of plasminogen to fibrin and its activation to plasmin. [HMDB]

laevo-norleucine hexanoic acid, 2-amino-, (S)-

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Articles:

laevo-norleucine
hexanoic acid, 2-amino-, (S)-